Nucleophilic Substitution at Tetracoordinate Phosphorus. Stereochemical Course and Mechanisms of Nucleophilic Displacement Reactions at Phosphorus in Diastereomeric cis- and trans-2-Halogeno-4-methyl-1,3,2-dioxaphosphorinan-2-thiones: Experimental and DFT Studies

Geometrical cis- and trans- isomers of 2-chloro-, 2-bromo- and 2-fluoro-4-methyl-1,3,2-dioxaphosphorinan-2-thiones were obtained in a diastereoselective way by (a) sulfurization of corresponding cyclic PIII-halogenides, (b) reaction of cyclic phosphorothioic acids with phosphorus pentachloride and (c) halogen–halogen exchange at PIV-halogenide. Their conformation and configuration at the C4-ring carbon and phosphorus stereocentres were studied by NMR (1H, 31P) methods, X-ray analysis and density functional (DFT) calculations. The stereochemistry of displacement reactions (alkaline hydrolysis, methanolysis, aminolysis) at phosphorus and its mechanism were shown to depend on the nature of halogen. Cyclic cis- and trans-isomers of chlorides and bromides react with nucleophiles (HO−, CH3O−, Me2NH) with inversion of configuration at phosphorus. DFT calculations provided evidence that alkaline hydrolysis of cyclic thiophosphoryl chlorides proceeds according to the SN2-P mechanism with a single transition state according to the potential energy surface (PES) observed. The alkaline hydrolysis reaction of cis- and trans-fluorides afforded the same mixture of the corresponding cyclic thiophosphoric acids with the thermodynamically more stable major product. Similar DFT calculations revealed that substitution at phosphorus in fluorides proceeds stepwise according to the A–E mechanism with formation of a pentacoordinate intermediate since a PES with two transition states was observed.


Introduction
The stereochemistry and mechanisms of nucleophilic substitution reactions at the phosphorus atom have been the major points of interest of many research groups since the middle of the last century [1]. The stereochemical course of nucleophilic displacement reactions at phosphorus has also been a subject of our early systematic studies, which have employed, in the first stage, optically active acyclic thiophosphonic acids 1 and their derivatives, as for example the enantiomeric thiophosphonyl chlorides 2 ( Figure 1).

Figure 1.
Structures of optically active acyclic thiophosphonic acid (1) and the corre thiophosphonyl chloride (2) used in studies of nucleophilic substitution at phospho These early investigations resulted, among others, in elaboration of a for thiophosphonic acids 1 (interconversion of the enantiomers of 1) [2,3] an unequivocal proof for the inversion of configuration at phosphorus occ chloride exchange reaction between radioactive chloride anion ( 36 Cl − ) and o thiophosphonyl chloride 2 [4]. It has also been demonstrated that alkaline optically active chlorides 2 proceeds with inversion at the P atom [5].
The second most important question about the mechanisms of reactions at phosphorus was, and it is still, whether these reactions occur s according to the SN2-P mechanism via a single transition state (TS) or ste addition-elimination mechanism (A-E) involving formation of pentacoordinate phosphorus intermediate (trigonal bipyramidal intermedia formed in the first reaction step by addition of the nucleophilic reage electrophilic phosphorus substrate and decomposes in the second step by of the leaving group (L) to the reaction product (see Scheme 1). Scheme 1. Mechanisms of nucleophilic substitution reactions at phosphorus and str possible pentacoordinate phosphorus intermediates (TBPI) formed by the A-E mec These early investigations resulted, among others, in elaboration of a Walden cycle for thiophosphonic acids 1 (interconversion of the enantiomers of 1) [2,3] and in providing unequivocal proof for the inversion of configuration at phosphorus occurring in the chloride exchange reaction between radioactive chloride anion ( 36 Cl − ) and optically active thiophosphonyl chloride 2 [4]. It has also been demonstrated that alkaline hydrolysis of optically active chlorides 2 proceeds with inversion at the P atom [5].
The second most important question about the mechanisms of displacement reactions at phosphorus was, and it is still, whether these reactions occur synchronously according to the S N 2-P mechanism via a single transition state (TS) or stepwise by the addition-elimination mechanism (A-E) involving formation of an unstable, pentacoordinate phosphorus intermediate (trigonal bipyramidal intermediate, TBPI). It is formed in the first reaction step by addition of the nucleophilic reagent (N) to the electrophilic phosphorus substrate and decomposes in the second step by the departure of the leaving group (L) to the reaction product (see Scheme 1). These early investigations resulted, among others, in elaboration of a Walden cycle for thiophosphonic acids 1 (interconversion of the enantiomers of 1) [2,3] and in providing unequivocal proof for the inversion of configuration at phosphorus occurring in the chloride exchange reaction between radioactive chloride anion ( 36 Cl − ) and optically active thiophosphonyl chloride 2 [4]. It has also been demonstrated that alkaline hydrolysis of optically active chlorides 2 proceeds with inversion at the P atom [5].
The second most important question about the mechanisms of displacement reactions at phosphorus was, and it is still, whether these reactions occur synchronously according to the SN2-P mechanism via a single transition state (TS) or stepwise by the addition-elimination mechanism (A-E) involving formation of an unstable, pentacoordinate phosphorus intermediate (trigonal bipyramidal intermediate, TBPI). It is formed in the first reaction step by addition of the nucleophilic reagent (N) to the electrophilic phosphorus substrate and decomposes in the second step by the departure of the leaving group (L) to the reaction product (see Scheme 1). In analogy with the SN2 substitution at carbon, the SN2-P reactions also occur with inversion of configuration. However, the relationship between the stereochemistry and the A-E mechanism is more complicated. It is now generally accepted that the stereochemical outcome of such stepwise reactions depends mainly on the disposal of the attacking N and leaving L groups in a short-living intermediate TBPI. Thus, the diapical or diequatorial disposal of N and L should lead to inversion of configuration at phosphorus while the stereochemical outcome of the apical-equatorial substitution is predicted to be retention. Moreover, these three different TBPIs may be formed as primary In analogy with the S N 2 substitution at carbon, the S N 2-P reactions also occur with inversion of configuration. However, the relationship between the stereochemistry and the A-E mechanism is more complicated. It is now generally accepted that the stereochemical outcome of such stepwise reactions depends mainly on the disposal of the attacking N and leaving L groups in a short-living intermediate TBPI. Thus, the diapical or diequatorial disposal of N and L should lead to inversion of configuration at phosphorus while the stereochemical outcome of the apical-equatorial substitution is predicted to be retention. Moreover, these three different TBPIs may be formed as primary intermediates or as a result of their pseudorotation. In this connection, it is necessary to emphasize a great importance of the Westheimer's concept [6] and his rules (apical entry of N, apical departure of L, microscopic reversibility and pseudorotation of TBPI) for understanding many aspects of nucleophilic substitution at phosphorus as well as at other heteroatoms such as sulfur [7]. The results of his careful studies on acid-catalyzed bidirectional hydrolysis of methyl ethylene phosphate 3 (2-methoxy-1,3,2-dioxaphospholan-2-one) and the concurrent rapid 16 O/ 18 O oxygen exchange in the phosphoryl group of 3 provided arguments for the A-E mechanism involving transient formation of a trigonal bipyramidal intermediate (TBPI-a) with the five-membered ring occupying the energetically most favorable apical-equatorial position and its Berry pseudorotation (BPR).
Although methyl ethylene phosphate 3 is an achiral molecule, an inspection of the pathway for the external hydrolysis of 3 and the oxygen 16 O/ 18 O exchange proposed by Westheimer strongly suggested that in cyclic five-membered phosphorus compounds the nucleophilic displacement reactions should occur with retention of configuration at P. This was found to be the case [8]. Using the geometrical cis and trans isomers of 2-chloro-4,5dimethyl-1,3,2-dioxaphospholan-2-thiones 4 as model compounds, we have demonstrated that the replacement of chloride anion in trans-4 by nucleophilic reagents N takes place with retention of configuration at phosphorus. This stereochemical outcome of the reaction was best rationalized in terms of the A-E mechanism shown in Scheme 2 and provided experimental, stereochemical evidence in support of the Westheimer's concept. intermediates or as a result of their pseudorotation. In this connection, it is necessary to emphasize a great importance of the Westheimer's concept [6]and his rules (apical entry of N, apical departure of L, microscopic reversibility and pseudorotation of TBPI) for understanding many aspects of nucleophilic substitution at phosphorus as well as at other heteroatoms such as sulfur [7]. The results of his careful studies on acid-catalyzed bidirectional hydrolysis of methyl ethylene phosphate 3 (2-methoxy-1,3,2dioxaphospholan-2-one) and the concurrent rapid 16 O/ 18 O oxygen exchange in the phosphoryl group of 3 provided arguments for the A-E mechanism involving transient formation of a trigonal bipyramidal intermediate (TBPI-a) with the five-membered ring occupying the energetically most favorable apical-equatorial position and its Berry pseudorotation (BPR). Although methyl ethylene phosphate 3 is an achiral molecule, an inspection of the pathway for the external hydrolysis of 3 and the oxygen 16 O/ 18 O exchange proposed by Westheimer strongly suggested that in cyclic five-membered phosphorus compounds the nucleophilic displacement reactions should occur with retention of configuration at P. This was found to be the case [8]. Using the geometrical cis and trans isomers of 2-chloro-4,5-dimethyl-1,3,2-dioxaphospholan-2-thiones 4 as model compounds, we have demonstrated that the replacement of chloride anion in trans-4 by nucleophilic reagents N takes place with retention of configuration at phosphorus. This stereochemical outcome of the reaction was best rationalized in terms of the A-E mechanism shown in Scheme 2 and provided experimental, stereochemical evidence in support of the Westheimer's concept. In the case of cyclic five-membered phosphorus compounds (1,3,2dioxaphospholanes), the ring occupies apical and equatorial position in the intermediate adduct (TBPI) since its diequatorial arrangement would cause a large steric strain [6]. This led to the question of the effect of a six-membered ring in 1,3,2-dioxaphosphorinanes on the stereochemical course and the mechanism of substitution at phosphorus. In this case, the diequatorial or apical-equatorial positions of the ring in the TBPI are equally probable and are not connected with the essential strain energy changes [9].The stereochemistry of the displacement reactions at phosphorus was intensively investigated using the geometrical cis-and trans-isomers of the structurally diverse 1,3,2-dioxaphosphorinanes shown in Figure 2.In this place, it is interesting to note that 1,3,2-dioxaphosphorinanes may be considered as oversimplified analogues of cyclic nucleotides-adenosine 3′,5′phosphate (c-AMP) and thiophosphate (c-AMPS). The elucidation of the mechanism of Scheme 2. Structure of methyl ethylene phosphate 3 and stereochemical course of displacement reactions at phosphorus in trans-2-chloro-4,5-dimethyl-1,3,2-dioxaphospholan-2-thione 4.
In the case of cyclic five-membered phosphorus compounds (1,3,2-dioxaphospholanes), the ring occupies apical and equatorial position in the intermediate adduct (TBPI) since its diequatorial arrangement would cause a large steric strain [6]. This led to the question of the effect of a six-membered ring in 1,3,2-dioxaphosphorinanes on the stereochemical course and the mechanism of substitution at phosphorus. In this case, the diequatorial or apical-equatorial positions of the ring in the TBPI are equally probable and are not connected with the essential strain energy changes [9].The stereochemistry of the displacement reactions at phosphorus was intensively investigated using the geometrical cisand trans-isomers of the structurally diverse 1,3,2-dioxaphosphorinanes shown in Figure 2. In this place, it is interesting to note that 1,3,2-dioxaphosphorinanes may be considered as oversimplified analogues of cyclic nucleotides-adenosine 3 ,5 -phosphate (c-AMP) and thiophosphate (c-AMPS). The elucidation of the mechanism of substitution at phosphorus could shed light on enzymatic hydrolytic processes of cyclic nucleotides.  The results of these very extensive studies on the stereochemistry of nucleophilic substitution reactions at phosphorus in 1,3,2-dioxaphosphorinanes, including also the synthesis of geometrical isomers and determination of their conformation, were summarized in a comprehensive review paper entitled "Stereochemical Aspects of Phosphorus-Containing Cyclohexanes" published in 1979 [10].
In general, the displacement reactions in 1,3,2-dioxaphosphorinanes investigated were found to occur with both inversion and retention at phosphorus. The stereochemical outcome depended on many factors like the nature of the entering and leaving group, solvent, added salts and reaction conditions. However, in spite of the fact that rich experimental material had been accumulated, it was not possible at that time to draw firm conclusions on the mechanism of the displacement reactions investigated. The results were explained by assuming operation of either the SN2 or A-E mechanisms. The best recapitulation of the results obtained in this early period may be found in one of the many papers devoted to the problem and is as follows: "The interpretation of our results is not a simple matter and should be accepted only as a starting point for further investigations" [11].
In our studies on the nucleophilic substitution reactions at phosphorus, the cis-and trans-isomers of 2-chloro-and 2-bromo-4-methyl-1,3,2-dioxaphosphorinan-2-ones (5) were used as model compounds ( Figure 3).  The results of these very extensive studies on the stereochemistry of nucleophilic substitution reactions at phosphorus in 1,3,2-dioxaphosphorinanes, including also the synthesis of geometrical isomers and determination of their conformation, were summarized in a comprehensive review paper entitled "Stereochemical Aspects of Phosphorus-Containing Cyclohexanes" published in 1979 [10].
In general, the displacement reactions in 1,3,2-dioxaphosphorinanes investigated were found to occur with both inversion and retention at phosphorus. The stereochemical outcome depended on many factors like the nature of the entering and leaving group, solvent, added salts and reaction conditions. However, in spite of the fact that rich experimental material had been accumulated, it was not possible at that time to draw firm conclusions on the mechanism of the displacement reactions investigated. The results were explained by assuming operation of either the S N 2 or A-E mechanisms. The best recapitulation of the results obtained in this early period may be found in one of the many papers devoted to the problem and is as follows: "The interpretation of our results is not a simple matter and should be accepted only as a starting point for further investigations" [11].
In our studies on the nucleophilic substitution reactions at phosphorus, the cisand trans-isomers of 2-chloro-and 2-bromo-4-methyl-1,3,2-dioxaphosphorinan-2-ones (5) were used as model compounds ( Figure 3).  The results of these very extensive studies on the stereochemistry of nucleophilic substitution reactions at phosphorus in 1,3,2-dioxaphosphorinanes, including also the synthesis of geometrical isomers and determination of their conformation, were summarized in a comprehensive review paper entitled "Stereochemical Aspects of Phosphorus-Containing Cyclohexanes" published in 1979 [10].
In general, the displacement reactions in 1,3,2-dioxaphosphorinanes investigated were found to occur with both inversion and retention at phosphorus. The stereochemical outcome depended on many factors like the nature of the entering and leaving group, solvent, added salts and reaction conditions. However, in spite of the fact that rich experimental material had been accumulated, it was not possible at that time to draw firm conclusions on the mechanism of the displacement reactions investigated. The results were explained by assuming operation of either the SN2 or A-E mechanisms. The best recapitulation of the results obtained in this early period may be found in one of the many papers devoted to the problem and is as follows: "The interpretation of our results is not a simple matter and should be accepted only as a starting point for further investigations" [11].
In our studies on the nucleophilic substitution reactions at phosphorus, the cis-and trans-isomers of 2-chloro-and 2-bromo-4-methyl-1,3,2-dioxaphosphorinan-2-ones (5) were used as model compounds ( Figure 3).  It was found that methanolysis and aminolysis occur with a full or predominant inversion of configuration [12]. The discussion of a possible mechanism of substitution at P was not conclusive and typical for all the papers at that time. Then, we prepared a new series of diastereomeric cyclic thiophosphoryl halogenides: trans-2-chloro-, trans-2bromo-and cis-2-fluoro-4-methyl-1,3,2-dioxaphosphorinan-2-thiones 6. In contrast to cyclic trans-chloride 6(Cl) and trans-bromide 6(Br), which reacted with nucleophilic reagents with inversion of configuration at phosphorus, cis-fluoride 6(F) was found to give, upon treatment with nucleophiles, a mixture of the corresponding isomeric products, the major one being formed with retention at phosphorus. These preliminary results reported in two short communications [13,14] did not allow us to unequivocally distinguish between a concerted S N 2-P substitution and an addition-elimination (A-E) mechanism. In general, it is difficult or impossible to make this distinction based only on stereochemical results. For instance, the observation of inversion of configuration at phosphorus may be explained not only by the S N 2-P mechanism but also by the A-E mechanism provided that the primarily formed trigonal bipyramidal phosphorane intermediate (TBPI) with nucleophilic reagent (N) and leaving groups (L) occupying apical positions undergoes decomposition to substitution product faster than pseudorotation.
Quite recently, we were able to solve these fundamental mechanistic questions in parallel studies on nucleophilic substitution at tetracoordinate sulfur [15]. We found that the results of kinetic studies of the chloride-chloride exchange reaction in arenesulfonyl chlorides in combination with the DFT computations of this identity reaction gave convincing evidence for operation of the S N 2-S mechanism with a single transition state. Similar DFT calculations for the fluoride exchange reaction in sulfonyl fluorides revealed that it proceeds stepwise according to the A-E mechanism with the formation of a pentacoordinate sulfur intermediate since a triple-well energy profile with two transition states was observed. The results mentioned above encouraged us to combine our stereochemical studies with theoretical calculations to definitely solve the question of the mechanism of substitution reactions at phosphorus (S N 2-P or A-E) in isomeric 2-halogeno-4-methyl-1,3,2dioxaphosphorinan-2-thiones 6. In the present paper we report the complete results of our studies on this class of compounds, including their stereospecific synthesis, stereochemical course of displacement reactions at phosphorus in 6 and the DFT calculations aimed at determination of the mechanisms of the substitution reactions. Our initial investigations were focused on the efficient preparation and assignment of stereochemistry (ring conformation, configuration of the C 4 and phosphorus stereocentres) to 2-chloro-, 2-bromo-and 2-fluoro-4-methyl-1,3,2-dioxaphosphorinan-2-thiones 6, which were intended to use as model compounds in subsequent studies of the stereochemistry of nucleophilic substitution at phosphorus.

Results and Discussion
At first, trans-2-chloro-4-methyl-1,3,2-dioxaphosphorinan-2-thione 6(Cl) was prepared by treatment of trans-2-chloro-4-methyl-1,3,2-dioxaphosphorinan 7 [16][17][18] with acetylsulfenyl chloride. The reaction was carried out in ether at 0 • C and afforded trans-6(Cl) as a pure diastereomer ( 31 P-NMR assay) in 91% yield (Scheme 3). This reaction, as other reactions of P III -compounds with sulfenyl chlorides [19], gave the desired product 6(Cl) in a stereospecific way with retention of configuration at phosphorus via the intermediate quasi-phosphonium chloride (A). Hence, the isomer of 6(Cl) obtained has the same trans-relation between the C4-methyl group and the chlorine atom This reaction, as other reactions of P III -compounds with sulfenyl chlorides [19], gave the desired product 6(Cl) in a stereospecific way with retention of configuration at phosphorus via the intermediate quasi-phosphonium chloride (A). Hence, the isomer of 6(Cl) obtained has the same trans-relation between the C 4 -methyl group and the chlorine atom as in the starting phosphorochloridite (7).
To gain more detailed insight into the ring stereochemistry and conformation the 270 MHz 1 H-NMR spectrum of trans-6(Cl) was recorded. It showed that all the resonance signals of the ring protons were well separated from each other, thus allowing the first order analysis of the spectrum without use of spin decoupling. In Table 1, all of the chemical shifts and coupling constants, derived from the spectrum, are summarized.  This reaction, as other reactions of P III -compounds with sulfenyl chlorides [19], gave the desired product 6(Cl) in a stereospecific way with retention of configuration at phosphorus via the intermediate quasi-phosphonium chloride (A). Hence, the isomer of 6(Cl) obtained has the same trans-relation between the C4-methyl group and the chlorine atom as in the starting phosphorochloridite (7).
To gain more detailed insight into the ring stereochemistry and conformation the 270 MHz 1 H-NMR spectrum of trans-6(Cl) was recorded. It showed that all the resonance signals of the ring protons were well separated from each other, thus allowing the first order analysis of the spectrum without use of spin decoupling. In Table 1, all of the chemical shifts and coupling constants, derived from the spectrum, are summarized. These values and particularly very distinct differences between the long-range 31 P-1 H couplings observed for axial and equatorial protons indicated that the dioxaphosphorinan ring in trans-6(Cl) adopts the chair conformation with the equatorial C4-methyl group and thiophosphoryl sulfur. Thus, the methyl protons appeared in the spectrum as a double doublet with coupling constants with the axial methine proton, 3 JCH3-CH = 6.2 Hz, and with phosphorus, 4 JCH3-P = 2.6 Hz. These values are diagnostic for equatorial position of the methyl group in the dioxaphosphorinan ring. The 31 P-NMR spectrum of trans-6(Cl) showed the resonance signal shaped like a double multiplet at δP = 59.0 ppm (see Figure  4, which is characteristic and typical for the 1,3,2-dioxaphosphorinan ring with the methyl group and thiophosphoryl sulfur in equatorial positions.) Interestingly, almost the same shape of the 31 P-spectrum was observed for the phosphoryl analogues of our compounds [12,20]. These values and particularly very distinct differences between the long-range 31 P-1 H couplings observed for axial and equatorial protons indicated that the dioxaphosphorinan ring in trans-6(Cl) adopts the chair conformation with the equatorial C 4 -methyl group and thiophosphoryl sulfur. Thus, the methyl protons appeared in the spectrum as a double doublet with coupling constants with the axial methine proton, 3 J CH3-CH = 6.2 Hz, and with phosphorus, 4 J CH3-P = 2.6 Hz. These values are diagnostic for equatorial position of the methyl group in the dioxaphosphorinan ring. The 31 P-NMR spectrum of trans-6(Cl) showed the resonance signal shaped like a double multiplet at δ P = 59.0 ppm (see Figure 4, which is characteristic and typical for the 1,3,2-dioxaphosphorinan ring with the methyl group and thiophosphoryl sulfur in equatorial positions.) Interestingly, almost the same shape of the 31 P-spectrum was observed for the phosphoryl analogues of our compounds [12,20].
The results of the chlorination reaction of diastereomeric thiophosphites 8 summarized in Scheme 4 indicated that the diastereomer trans-6(Cl) is thermodynamically more stable than cis-6(Cl) and that epimerization at phosphorus was occurring in the reaction course. A possibility of epimerization of the starting thiophosphites 8 (trans-8→cis-8) was excluded since treatment of a 1:1 mixture of isomeric 8 with gaseous hydrogen chloride under the reaction conditions comparable to the chlorination reaction did not affect the isomeric ratio of 8. Most probably, cis-6(Cl), when formed from trans-8, undergoes conversion to the more stable trans-6(Cl) via the chloride-chloride exchange reaction at phosphorus as shown below (Scheme 5). The results of the chlorination reaction of diastereomeric thiophosphites 8 summarized in Scheme 4 indicated that the diastereomer trans-6(Cl) is thermodynamically more stable than cis-6(Cl) and that epimerization at phosphorus was occurring in the reaction course. A possibility of epimerization of the starting thiophosphites 8 (trans-8→cis-8) was excluded since treatment of a 1:1 mixture of isomeric 8 with gaseous hydrogen chloride under the reaction conditions comparable to the chlorination reaction did not affect the isomeric ratio of 8. Most probably, cis-6(Cl), when formed from trans-8, undergoes conversion to the more stable trans-6(Cl) via the chloride-chloride exchange reaction at phosphorus as shown below (Scheme 5). The observation of a fully stereospecific formation of trans-6(Cl) upon chlorination of a mixture of isomeric thiophosphites 8 prompted us to investigate their bromination (Scheme 6). It was found that the reaction of thiophosphite 8 consisting of 73% trans-8 and 27% cis-8 with elemental bromine carried out at 30 °C in benzene gave only one crystalline isomer of phosphorobromidate trans-6(Br) in 85% yield. As in the case of trans-6(Cl), the C4-methyl protons of the crystalline isomer appeared in 1 H-NMR spectrum as a double doublet with characteristic coupling constants, 3 JCH3-H = 6.9 Hz and 4 JCH3-P = 2.9 Hz, indicating that it exists in a chair conformation with both the C4-methyl and P=S groups in equatorial position. Moreover, Figure 4 shows that the shape of the resonance signal in the 31 P-NMR spectrum of the more stable crystalline thiophosphoryl bromide trans-6(Br) is almost the same as that of the corresponding chloride trans-6(Cl). When the same mixture of isomeric thiophosphites 8 was reacted with bromine at −15°C, a mixture of both isomeric phosphorobromidates was formed, i.e., trans-6(Br) (64%) and cis-6(Br) (36%). The observation of a fully stereospecific formation of trans-6(Cl) upon chlorination of a mixture of isomeric thiophosphites 8 prompted us to investigate their bromination (Scheme 6). It was found that the reaction of thiophosphite 8 consisting of 73% trans-8 and 27% cis-8 with elemental bromine carried out at 30 • C in benzene gave only one crystalline isomer of phosphorobromidate trans-6(Br) in 85% yield. As in the case of trans-6(Cl), the C 4 -methyl protons of the crystalline isomer appeared in 1 H-NMR spectrum as a double doublet with characteristic coupling constants, 3 J CH3-H = 6.9 Hz and 4 J CH3-P = 2.9 Hz, indicating that it exists in a chair conformation with both the C 4 -methyl and P=S groups in equatorial position. Moreover, Figure 4 shows that the shape of the resonance signal in the 31 P-NMR spectrum of the more stable crystalline thiophosphoryl bromide trans-6(Br) is almost the same as that of the corresponding chloride trans-6(Cl). When the same mixture of isomeric thiophosphites 8 was reacted with bromine at −15 • C, a mixture of both isomeric phosphorobromidates was formed, i.e., trans-6(Br) (64%) and cis-6(Br) (36%). In search of a stereospecific synthesis of the less stable cyclic thiophosphoryl chloride cis-6(Cl), we turned our attention on the reaction of monothiophosphoric acids with phosphorus pentachloride. This reaction with the enantiomers of thiophosphonic acid 1 afforded exclusively enantiomerically pure thiophosphonyl chlorides 2 with inversion of configuration [2,4,22].In the hope that cyclic monothiophosphoric acids will react with phosphorus pentachloride in a similar way, the reaction of easily available cis-and trans-2-hydroxy-4-methyl-1,3,2-dioxaphosphorinan-2-thiones 9 [23]withthis reagent was inves-Scheme 6. Stereospecific synthesis of trans-2-bromo-4-methyl-1,3,2-dioxaphosphorinan-2-thione 6(Br).
In search of a stereospecific synthesis of the less stable cyclic thiophosphoryl chloride cis-6(Cl), we turned our attention on the reaction of monothiophosphoric acids with phosphorus pentachloride. This reaction with the enantiomers of thiophosphonic acid 1 afforded exclusively enantiomerically pure thiophosphonyl chlorides 2 with inversion of configuration [2,4,22].In the hope that cyclic monothiophosphoric acids will react with phosphorus pentachloride in a similar way, the reaction of easily available cis-and trans-2-hydroxy-4-methyl-1,3,2-dioxaphosphorinan-2-thiones 9 [23]withthis reagent was investigated. However, we were surprised to find that in addition to the expected isomeric chlorides 6(Cl), two other products were formed. Their structures were dependent on the configuration at phosphorus in starting cyclic thioacids 9. Thus, treatment of trans-9 with PCl5 suspended in benzene at 0-5 °C resulted in formation of three products as revealed by 31 P-NMR spectra: thiophosphoryl chloride (trans-6(Cl), phosphoryl chloride trans-5(Cl) and unsymmetrical trans-cis-dithiopyrophosphate 10 (see Scheme 7). Scheme 7. Structure of products formed in reaction between phosphorus pentachloride and thiophosphoric acid trans-9. Scheme 7. Structure of products formed in reaction between phosphorus pentachloride and thiophosphoric acid trans-9.
The formation of thiophosphoryl chloride trans-6(Cl) in this reaction was expected as well as the fact that it was formed from thioacid trans-9 with inversion of configuration at phosphorus. However, the appearance of phosphorochloridate trans-5(Cl) among the reaction products was astonishing. Moreover, the replacement of sulfur in trans-9 by chlorine leading to trans-5(Cl) was occurring with retention at phosphorus. The third product was identified as one of the three isomeric bis-(4-methyl-1,3,2-dioxaphosphorinan-2-thionyl)oxides 10. Their synthesis, configuration and conformation were reported in a separate paper [24].
A somewhat different outcome of the reaction of thioacid cis-9 with PCl 5 was observed. To our satisfaction the major product in this case was the desired thermodynamically less stable thiophosphoryl chloride cis-6(Cl) formed in 60% yield. It was accompanied by the more stable isomer trans-6(Cl) (21%). The latter was undoubtedly the product of epimerization at phosphorus in cis-6(Cl) taking place in the presence of chloride anions in a reaction mixture. Interestingly, the same dithiopyrophosphate trans-cis-10 was also formed in this reaction in comparable amounts (19%) (Scheme 8). Distillation of a mixture of these three reaction products allowed us to isolate thiophosphoryl chloride cis-6(Cl) containing 5% trans-isomer as the lowest boiling fraction. This almost diastereomerically pure cis-chloride 6 was used in our further experiments. nied by the more stable isomer trans-6(Cl) (21%). The latter was undoubtedly the product of epimerization at phosphorus in cis-6(Cl) taking place in the presence of chloride anions in a reaction mixture. Interestingly, the same dithiopyrophosphate trans-cis-10 was also formed in this reaction in comparable amounts (19%) (Scheme 8). Distillation of a mixture of these three reaction products allowed us to isolate thiophosphoryl chloride cis-6(Cl) containing 5% trans-isomer as the lowest boiling fraction. This almost diastereomerically pure cis-chloride 6 was used in our further experiments. Scheme 8. Structure of products formed in reaction between phosphorus pentachloride and thiophosphoric acid cis-9.
Although elucidation of all mechanistic details of the reaction under discussion was beyond the scope of the present work, we wish to rationalize herein its multidirectional course and stereochemistry of the products formation (Scheme 9). Taking into account the well-known ambident reactivity of monothiophosphoric acids and their anions, it is reasonable to assume that cyclic thioacids, like acyclic ones, react with phosphorus pentachloride at the oxygen atom. This initial reaction, for example with trans-9, results in formation of O-trichlorophosphonium chloride (A) as the first reaction intermediate. This, in turn, upon a nucleophilic attack of the chloride anion at the phosphorinanyl phosphorus and the concomitant four-membered ring closure between sulfur and the trichlorophosphonium phosphorus atom, is converted into a second intermediate (B). Its formation and relative stability are due to the presence of two six-and four-membered rings, which are known to stabilize hypervalent phosphorus compounds. Interestingly, almost Scheme 8. Structure of products formed in reaction between phosphorus pentachloride and thiophosphoric acid cis-9.
Although elucidation of all mechanistic details of the reaction under discussion was beyond the scope of the present work, we wish to rationalize herein its multidirectional course and stereochemistry of the products formation (Scheme 9). Taking into account the well-known ambident reactivity of monothiophosphoric acids and their anions, it is reasonable to assume that cyclic thioacids, like acyclic ones, react with phosphorus pentachloride at the oxygen atom. This initial reaction, for example with trans-9, results in formation of O-trichlorophosphonium chloride (A) as the first reaction intermediate. This, in turn, upon a nucleophilic attack of the chloride anion at the phosphorinanyl phosphorus and the concomitant four-membered ring closure between sulfur and the trichlorophosphonium phosphorus atom, is converted into a second intermediate (B). Its formation and relative stability are due to the presence of two six-and four-membered rings, which are known to stabilize hypervalent phosphorus compounds. Interestingly, almost the same type of structure was postulated for the intermediate found in the reaction between oxophosphoranesulfenyl chlorides and phosphorus trichloride [25]. This trigonal bipyramidal intermediate (B) may undergo decomposition in two ways. The first accompanied by elimination of phosphoryl trichloride affords the expected thiophosphoryl chloride trans-6(Cl) with the experimentally confirmed inversion of configuration. On the other hand, simultaneous elimination of thiophosphoryl trichloride from (B) results in formation of the unexpected phosphoryl chloride trans-5(Cl) with retention of configuration at phosphorus. This stereochemistry of the conversion trans-9→trans-5(Cl) is also in a full agreement with that experimentally found (see Scheme 9). Finally, the formation of dithiopyrophosphate 10 as a third reaction product is worthy of notice. It is undoubtedly formed in the reaction between starting thioacid trans-9 and the first reaction intermediate (A). The latter, having a good leaving group, undergoes nucleophilic substitution by thioacid trans-9 with inversion of configuration at phosphorus, which affords unsymmetrical trans-cis-diastereomer of dithiopyrophosphate 10.
To complete the synthesis of cyclic thiophosphoryl halogenides 6(Cl, Br, F) and having some experience with the preparation of chlorides 6(Cl) and bromides 6(Br), we turned to the synthesis of diastereomeric fluorides 6(F). In general, the synthetic approaches to acyclic and cyclic thiophosphoryl fluorides are sparse and of limited applicability. The most practical method of their synthesis involves the halogen exchange reaction at phosphorus using inorganic fluorides [3,26]. In our first attempt to obtain 6(F), a very simple reaction was tested, namely, the addition of elemental sulfur to cyclic fluorophosphite 11. The latter was prepared according to the modified procedure described by Schmutzler [27] from trans-chlorophosphite 7 and antimony trifluoride (Scheme 10).

Scheme 9.
Proposed course of reaction between thioacid trans-9 and phosphorus pentachloride. This trigonal bipyramidal intermediate (B) may undergo decomposition in two ways. The first accompanied by elimination of phosphoryl trichloride affords the expected thiophosphoryl chloride trans-6(Cl) with the experimentally confirmed inversion of configuration. On the other hand, simultaneous elimination of thiophosphoryl trichloride from (B) results in formation of the unexpected phosphoryl chloride trans-5(Cl) with retention of configuration at phosphorus. This stereochemistry of the conversion trans-9→trans-5(Cl) is also in a full agreement with that experimentally found (see Scheme 9). Finally, the formation of dithiopyrophosphate 10 as a third reaction product is worthy of notice. It is undoubtedly formed in the reaction between starting thioacid trans-9 and the first reaction intermediate (A). The latter, having a good leaving group, undergoes nucleophilic substitution by thioacid trans-9 with inversion of configuration at phosphorus, which affords unsymmetrical trans-cis-diastereomer of dithiopyrophosphate 10.
To complete the synthesis of cyclic thiophosphoryl halogenides 6(Cl, Br, F) and having some experience with the preparation of chlorides 6(Cl) and bromides 6(Br), we turned to the synthesis of diastereomeric fluorides 6(F). In general, the synthetic approaches to acyclic and cyclic thiophosphoryl fluorides are sparse and of limited applicability. The most practical method of their synthesis involves the halogen exchange reaction at phosphorus using inorganic fluorides [3,26]. In our first attempt to obtain 6(F), a very simple reaction was tested, namely, the addition of elemental sulfur to cyclic fluorophosphite 11. The latter was prepared according to the modified procedure described by Schmutzler [27] from trans-chlorophosphite 7 and antimony trifluoride (Scheme 10). Trans-fluorophosphite 11 as a major and thermodynamically more stable product obtained in this reaction was contaminated with 5% cis-isomer. To our surprise, it was found that the addition of elemental sulfur to trans-11 does not occur even in boiling toluene. When, however, acetylsulfenyl chloride was used instead of elemental sulfur, the conversion of trans-11 to cis-6(F) was achieved efficiently under mild reaction conditions (Scheme 11). Trans-fluorophosphite 11 as a major and thermodynamically more stable product obtained in this reaction was contaminated with 5% cis-isomer. To our surprise, it was found that the addition of elemental sulfur to trans-11 does not occur even in boiling toluene. When, however, acetylsulfenyl chloride was used instead of elemental sulfur, the conversion of trans-11 to cis-6(F) was achieved efficiently under mild reaction conditions (Scheme 11). Scheme 11. Synthesis of thiophosphoryl fluoride 6(F).
As expected, the sulfurization of trans-fluorophosphite 11 occurred with a full retention of configuration at phosphorus and afforded the crude thiophosphoryl fluoride cis-6(F) containing 5% of trans-6(F). The diastereomerically pure solid cis-isomer (m.p. 33-34 °C) was isolated from this mixture by distillation and crystallization. The NMR ( 1 H, 31 P) data of cis-fluoride 6(F) were consistent with a rigid chair conformation in which the thiophosphoryl sulfur and the methyl group on C4 are in equatorial positions on the 1,3,2dioxaphosphorinan ring. For instance, the resonance signal (double doublet) of the methyl protons with characteristic coupling constants, 3 JCH3-H = 6.2 Hz and 4 JCH3-P = 2.6 Hz, shows that the methyl group is equatorial. The 31 P-NMR spectrum of cis-6(F) shows a typical doublet with the coupling constant 1 JP-F= 1086 Hz due to the presence of fluorine directly bonded to phosphorus. The shape of each arm of this doublet is almost identical with the 31 P-NMR resonance signals of trans-6(Cl) and trans-6(Br) (see Figure 1). This observation may be taken as additional evidence that all the thiophosphoryl halogenides mentioned above exist in the same chair conformation with the equatorial C4-methyl and thiophos-Scheme 11. Synthesis of thiophosphoryl fluoride 6(F).
As expected, the sulfurization of trans-fluorophosphite 11 occurred with a full retention of configuration at phosphorus and afforded the crude thiophosphoryl fluoride cis-6(F) containing 5% of trans-6(F). The diastereomerically pure solid cis-isomer (m.p. 33-34 • C) was isolated from this mixture by distillation and crystallization. The NMR ( 1 H, 31 P) data of cis-fluoride 6(F) were consistent with a rigid chair conformation in which the thiophosphoryl sulfur and the methyl group on C 4 are in equatorial positions on the 1,3,2dioxaphosphorinan ring. For instance, the resonance signal (double doublet) of the methyl protons with characteristic coupling constants, 3 J CH3-H = 6.2 Hz and 4 J CH3-P = 2.6 Hz, shows that the methyl group is equatorial. The 31 P-NMR spectrum of cis-6(F) shows a typical doublet with the coupling constant 1 J P-F = 1086 Hz due to the presence of fluorine directly bonded to phosphorus. The shape of each arm of this doublet is almost identical with the 31 P-NMR resonance signals of trans-6(Cl) and trans-6(Br) (see Figure 1). This observation may be taken as additional evidence that all the thiophosphoryl halogenides mentioned above exist in the same chair conformation with the equatorial C 4 -methyl and thiophosphoryl group. Finally, a single-crystal X-ray analysis of cis-6(F) revealed [28] that the 1,3,2dioxaphosphorinan ring also adopts a chair conformation in the solid state and confirmed our configurational assignments based on NMR measurements (see Figures 2 and 5). 6(F) containing 5% of trans-6(F). The diastereomerically pure solid cis-isomer (m.p. 33-34 °C) was isolated from this mixture by distillation and crystallization. The NMR ( 1 H, 31 P) data of cis-fluoride 6(F) were consistent with a rigid chair conformation in which the thiophosphoryl sulfur and the methyl group on C4 are in equatorial positions on the 1,3,2dioxaphosphorinan ring. For instance, the resonance signal (double doublet) of the methyl protons with characteristic coupling constants, 3 JCH3-H = 6.2 Hz and 4 JCH3-P = 2.6 Hz, shows that the methyl group is equatorial. The 31 P-NMR spectrum of cis-6(F) shows a typical doublet with the coupling constant 1 JP-F= 1086 Hz due to the presence of fluorine directly bonded to phosphorus. The shape of each arm of this doublet is almost identical with the 31 P-NMR resonance signals of trans-6(Cl) and trans-6(Br) (see Figure 1). This observation may be taken as additional evidence that all the thiophosphoryl halogenides mentioned above exist in the same chair conformation with the equatorial C4-methyl and thiophosphoryl group. Finally, a single-crystal X-ray analysis of cis-6(F) revealed [28] that the 1,3,2dioxaphosphorinan ring also adopts a chair conformation in the solid state and confirmed our configurational assignments based on NMR measurements (see Figures 2 and 5).  The trans-isomer of 6(F) was obtained from trans-bromide 6(Br) and ammonium fluoride. The bromide → fluoride exchange reaction carried out in acetonitrile solution at 40 • C afforded after 8 h a mixture of transand cis-fluorides at a ratio of 84:16. When the reaction was conducted for 24 h at the same temperature, the desired trans-fluoride 6(F) was formed with inversion of configuration and with 94% diastereomeric purity. The diastereomerically pure trans-6(F) was obtained by preparative gas chromatography. However, prolongation of the reaction time to 50 h resulted in the isomerization of trans-6(F) (inversion of configuration at P) to the thermodynamically more stable cis-6(F) and the latter was formed with 83% diastereomeric purity (Scheme 12). The trans-isomer of 6(F) was obtained from trans-bromide 6(Br) and ammonium fluoride. The bromide → fluoride exchange reaction carried out in acetonitrile solution at 40 °C afforded after 8 h a mixture of trans-and cis-fluorides at a ratio of 84:16. When the reaction was conducted for 24 h at the same temperature, the desired trans-fluoride 6(F) was formed with inversion of configuration and with 94% diastereomeric purity. The diastereomerically pure trans-6(F) was obtained by preparative gas chromatography. However, prolongation of the reaction time to 50 h resulted in the isomerization of trans-6(F) (inversion of configuration at P) to the thermodynamically more stable cis-6(F) and the latter was formed with 83% diastereomeric purity (Scheme 12). Scheme 12. Synthesis of thiophosphoryl fluoride trans-6(F) and its epimerization to cis-6(F).
Most probably, the above fluoride-fluoride exchange reaction should lead to the diastereomerically pure cis-6(F) after longer heating. Moreover, the fact that a trace of the less stable trans-6(F) was not observed when the pure fluoride cis-6(F) was heated with NH4F (60 h, 40 °C) indicates that this identity reaction reflects a strong preference of fluorine for an axial position versus a P=S bond in the 1,3,2-dioxaphosphorinan ring. DFT calculations show that the trans-6(F) isomer has a free energy of ΔG = 2.5 kcal/mol higher than cis-6(F) isomer, which corresponds roughly to an equilibrium concentration ratio [trans-6(F)]eq/[cis-6(F)]eq of ca. 1.5 × 10 −2 . Taking into account 1 H-and 31 P-NMR data, as well as DFT calculations (see Supplementary Materials), it is reasonable to assume that the trans-6(F) isomer exists in two chair conformations (A and B) and one boat conformation(C) that are in a fast equilibrium as shown below (Scheme 13). Most probably, the above fluoride-fluoride exchange reaction should lead to the diastereomerically pure cis-6(F) after longer heating. Moreover, the fact that a trace of the less stable trans-6(F) was not observed when the pure fluoride cis-6(F) was heated with NH 4 F (60 h, 40 • C) indicates that this identity reaction reflects a strong preference of fluorine for an axial position versus a P=S bond in the 1,3,2-dioxaphosphorinan ring. DFT calculations show that the trans-6(F) isomer has a free energy of ∆G = 2.5 kcal/mol higher than cis-6(F) isomer, which corresponds roughly to an equilibrium concentration ratio [trans-6(F)] eq /[cis-6(F)] eq of ca. 1.5 × 10 −2 . Taking into account 1 H-and 31 P-NMR data, as well as DFT calculations (see Supplementary Materials), it is reasonable to assume that the trans-6(F) isomer exists in two chair conformations (A and B) and one boat conformation(C) that are in a fast equilibrium as shown below (Scheme 13).
Most probably, the above fluoride-fluoride exchange reaction should lead to the diastereomerically pure cis-6(F) after longer heating. Moreover, the fact that a trace of the less stable trans-6(F) was not observed when the pure fluoride cis-6(F) was heated with NH4F (60 h, 40 °C) indicates that this identity reaction reflects a strong preference of fluorine for an axial position versus a P=S bond in the 1,3,2-dioxaphosphorinan ring. DFT calculations show that the trans-6(F) isomer has a free energy of ΔG = 2.5 kcal/mol higher than cis-6(F) isomer, which corresponds roughly to an equilibrium concentration ratio [trans-6(F)]eq/[cis-6(F)]eq of ca. 1.5 × 10 −2 . Taking into account 1 H-and 31 P-NMR data, as well as DFT calculations (see Supplementary Materials), it is reasonable to assume that the trans-6(F) isomer exists in two chair conformations (A and B) and one boat conformation(C) that are in a fast equilibrium as shown below (Scheme 13). Scheme 13. Conformational equilibrium in trans-6(F).
The conformer (B) with the axial methyl group at C4 should be present in equilibrium in substantial proportions, which is reflected in the different shape of the diagnostic 1 H-NMR resonance signal of the C4-Me from that of the cis-isomer 6(F). Thus, the methyl protons of trans-6(F) appeared in the spectrum as a doublet of triplets due to characteristic splitting by the C4-proton ( 3 JCH3-H = 6.5 Hz), then by phosphorus ( 4 JCH3-P = 0.9 Hz) and additionally by the vicinal axial proton at C5 with the same coupling constant value (0.9 Hz) as with phosphorus. The observation of the last coupling and a small value of the coupling constant with phosphorus is indicative of the presence of the conformer (B) in equilibrium. On the other hand, the 31 P-NMR spectrum of trans-6(F) shows a typical doublet due to splitting by fluorine with the coupling constant 1 JP-F = 1094 Hz. Both arms of this doublet are dense multiplets, which are characteristic of the dioxaphosphorinan rings, having methyl and thiophosphoryl groups trans situated. The 31 P-NMR spectra of a mixture of trans-6(F) (84%) and cis-6(F) (16%) (shown in Figure 5) in conjunction with Figure 4 best illustrate the relationship between the shape of the 31 P-NMR resonance signals and configuration at phosphorus and C4-carbon in the 1,3,2-dioxaphosphorinan systems. The conformer (B) with the axial methyl group at C 4 should be present in equilibrium in substantial proportions, which is reflected in the different shape of the diagnostic 1 H-NMR resonance signal of the C 4 -Me from that of the cis-isomer 6(F). Thus, the methyl protons of trans-6(F) appeared in the spectrum as a doublet of triplets due to characteristic splitting by the C 4 -proton ( 3 J CH3-H = 6.5 Hz), then by phosphorus ( 4 J CH3-P = 0.9 Hz) and additionally by the vicinal axial proton at C 5 with the same coupling constant value (0.9 Hz) as with phosphorus. The observation of the last coupling and a small value of the coupling constant with phosphorus is indicative of the presence of the conformer (B) in equilibrium. On the other hand, the 31 P-NMR spectrum of trans-6(F) shows a typical doublet due to splitting by fluorine with the coupling constant 1 J P-F = 1094 Hz. Both arms of this doublet are dense multiplets, which are characteristic of the dioxaphosphorinan rings, having methyl and thiophosphoryl groups trans situated. The 31 P-NMR spectra of a mixture of trans-6(F) (84%) and cis-6(F) (16%) (shown in Figure 5) in conjunction with Figure 4 best illustrate the relationship between the shape of the 31 P-NMR resonance signals and configuration at phosphorus and C 4 -carbon in the 1,3,2-dioxaphosphorinan systems.
These observations are supported by our DFT calculations. We performed full conformational analysis of one pair of diastereomers, namely (R P ,S C4 ) and (S P ,S C4 ), as the other pair, (S P ,R C4 ) and (R P ,R C4 ), respectively, are their equivalent enantiomeric forms. For both diastereomers, two stable low energy chair conformations and one boat conformation were identified. The structures and relative free energies of the cisand trans-conformers of 6(F) in aqueous solution (in kcal/mol) are given in Supplementary Materials, Figure S2 and Table S2. The calculated geometry of cis-2-fluoro-4-methyl-1,3,2-dioxaphosphorinan-2-thione in the aqueous solution agrees very well with its crystal structure reported [24], which proves the reliability of the theoretical method used (Supplementary Materials, Table S4).
The most stable conformer of the two diastereomers (Scheme 11) is the conformer cis-6(F) in which fluorine occupies an axial position and the methyl group on the C 4 carbon occupies an equatorial position.

Stereochemistry of Nucleophilic Displacement Reactions at Phosphorus in 2-Halogeno-4-methyl-1,3,2-dioxaphosphorinan-2-thiones 6
Having in hand the diastereomeric pairs of thiophosphoryl chloride 6(Cl) and fluoride 6(F), we could start with investigation of the stereochemical course of nucleophilic displacement processes occurring at phosphorus. In the present work, three basic substitution reactions were examined, namely alkaline hydrolysis, methanolysis and aminolysis. The choice of the first two reactions was due to the fact that they produce diastereomeric thioacids 9 [23] and thionophosphates 12 [19], respectively, which were obtained by us in an independent way and the configuration at phosphorus in both diastereomers of 9 and 12 was firmly established. Moreover, the diastereomeric hydrolysis products 9 as well as thiophosphoryl amides 13 formed in the third reaction do not undergo epimerization at phosphorus under the reaction conditions. At first, the stereochemical course of displacement reactions at phosphorus in the trans-isomer of thiophosphoryl chloride 6(Cl) was investigated. The results obtained are summarized in Scheme 14. us in an independent way and the configuration at phosphorus in both diastereomers of 9 and 12 was firmly established. Moreover, the diastereomeric hydrolysis products 9 as well as thiophosphoryl amides 13 formed in the third reaction do not undergo epimerization at phosphorus under the reaction conditions. At first, the stereochemical course of displacement reactions at phosphorus in the trans-isomer of thiophosphoryl chloride 6(Cl) was investigated. The results obtained are summarized in Scheme 14.
Alkaline hydrolysis of the diastereomerically pure trans-6(Cl) as well as other halogenides 6 was carried out in a water-dioxane solution at ca. 0 • C. The crude sodium salt of thioacid 9 isolated from the reaction mixture showed two resonance signals at δ P = 50.5 and 54.0 ppm in the 31 P-NMR spectrum, corresponding to the sodium salts of thioacid trans-9 and cis-9, respectively. They were formed in a 92:8 ratio. For further identification and characterization, this mixture of both sodium salts was converted into the corresponding dicyclohexyl ammonium salts of trans-9 (92%) and cis-9 (8%) displaying chemical shifts at δ P = 50.5 and 53.5 ppm. The fact that thioacid trans-9 was formed as the major hydrolysis product indicates that the reaction under discussion occurred with inversion of configuration at phosphorus. A very small amount (8%) of thioacid cis-9 formed in this reaction may be explained by a concomitant formation of cis-6(Cl) (via the chloride-chloride exchange reaction in the starting trans-6(Cl)) and its subsequent hydrolysis to cis-9. Alkaline hydrolysis of the thermodynamically less stable thiophosphoryl chloride cis-6(Cl) with 95% diastereomeric purity afforded a mixture of two sodium salts of thioacid cis-9 and trans-9 in a 77:23 ratio as revealed by 31 P-NMR spectrum. Formation of the sodium salt of cis-9 as the major product also demonstrated the prevailing stereoinvertive course of hydrolysis of this stereomer (Scheme 15).

Molecules 2021, 26, x FOR PEER REVIEW 15 of 30
Alkaline hydrolysis of the diastereomerically pure trans-6(Cl) as well as other halogenides 6 was carried out in a water-dioxane solution at ca. 0 °C. The crude sodium salt of thioacid 9 isolated from the reaction mixture showed two resonance signals at δP = 50.5 and 54.0 ppm in the 31 P-NMR spectrum, corresponding to the sodium salts of thioacid trans-9 and cis-9, respectively. They were formed in a 92:8 ratio. For further identification and characterization, this mixture of both sodium salts was converted into the corresponding dicyclohexyl ammonium salts of trans-9 (92%) and cis-9 (8%) displaying chemical shifts at δP = 50.5 and 53.5 ppm. The fact that thioacid trans-9 was formed as the major hydrolysis product indicates that the reaction under discussion occurred with inversion of configuration at phosphorus. A very small amount (8%) of thioacid cis-9 formed in this reaction may be explained by a concomitant formation of cis-6(Cl) (via the chloride-chloride exchange reaction in the starting trans-6(Cl)) and its subsequent hydrolysis to cis-9. Alkaline hydrolysis of the thermodynamically less stable thiophosphoryl chloride cis-6(Cl) with 95% diastereomeric purity afforded a mixture of two sodium salts of thioacid cis-9 and trans-9 in a 77:23 ratio as revealed by 31 P-NMR spectrum. Formation of the sodium salt of cis-9 as the major product also demonstrated the prevailing stereoinvertive course of hydrolysis of this stereomer (Scheme 15). The methanolysis reaction of trans-6(Cl) was carried out in a mixture of benzene and sodium methoxide in methanol at 0 °C. It afforded the cyclic thionophosphate trans-12 with 93% diastereomeric purity ( 31 P-NMR assay). As in the case of alkaline hydrolysis of trans-6(Cl), the stereochemical outcome of the methanolysis was also inversion of configuration at phosphorus. However, in this case a small decrease of diastereoselectivity in this reaction may be due to the methoxy-methoxy exchange reaction at phosphorus in trans-12, resulting in formation of cis-12, the more thermodynamically stable isomer.
In contrast to alkaline hydrolysis and methanolysis, the reaction of trans-6(Cl) with dimethylamine in ether at 0 °C gave the corresponding thiophosphoryl amide trans-13 with complete inversion of configuration at phosphorus. As the aminolysis product (trans- The methanolysis reaction of trans-6(Cl) was carried out in a mixture of benzene and sodium methoxide in methanol at 0 • C. It afforded the cyclic thionophosphate trans-12 with 93% diastereomeric purity ( 31 P-NMR assay). As in the case of alkaline hydrolysis of trans-6(Cl), the stereochemical outcome of the methanolysis was also inversion of configuration at phosphorus. However, in this case a small decrease of diastereoselectivity in this reaction may be due to the methoxy-methoxy exchange reaction at phosphorus in trans-12, resulting in formation of cis-12, the more thermodynamically stable isomer.
In contrast to alkaline hydrolysis and methanolysis, the reaction of trans-6(Cl) with dimethylamine in ether at 0 • C gave the corresponding thiophosphoryl amide trans-13 with complete inversion of configuration at phosphorus. As the aminolysis product (trans-13) was not reported in the literature, it was prepared by us in an independent way starting from cis-2-dimethylamino-4-methyl-1,3,2-dioxaphosphorinan 14 (80% dp) [29], which upon treatment with acetylsulfenyl chloride gave thiophosphoryl amide trans-13 with 94% diastereomeric purity. Addition of elemental sulfur to amidophosphite 14 also occurred with retention of configuration at phosphorus and afforded trans-13 with 82% diastereomeric purity (Scheme 16).
The methanolysis reaction of trans-6(Cl) was carried out in a mixture of benzene and sodium methoxide in methanol at 0 °C. It afforded the cyclic thionophosphate trans-12 with 93% diastereomeric purity ( 31 P-NMR assay). As in the case of alkaline hydrolysis of trans-6(Cl), the stereochemical outcome of the methanolysis was also inversion of configuration at phosphorus. However, in this case a small decrease of diastereoselectivity in this reaction may be due to the methoxy-methoxy exchange reaction at phosphorus in trans-12, resulting in formation of cis-12, the more thermodynamically stable isomer.
In contrast to alkaline hydrolysis and methanolysis, the reaction of trans-6(Cl) with dimethylamine in ether at 0 °C gave the corresponding thiophosphoryl amide trans-13 with complete inversion of configuration at phosphorus. As the aminolysis product (trans-13) was not reported in the literature, it was prepared by us in an independent way starting from cis-2-dimethylamino-4-methyl-1,3,2-dioxaphosphorinan 14 (80% dp) [29], which upon treatment with acetylsulfenyl chloride gave thiophosphoryl amide trans-13 with 94% diastereomeric purity. Addition of elemental sulfur to amidophosphite 14 also occurred with retention of configuration at phosphorus and afforded trans-13 with 82% diastereomeric purity (Scheme 16). Similar results were obtained with the thiophosphoryl bromide trans-6(Br), which was used as a substrate in the three substitution reactions investigated herein (see Scheme 14). Thus, alkaline hydrolysis and methanolysis of this bromide were found to occur with a predominant inversion of configuration at phosphorus while aminolysis, as in the case of the trans-chloride 6(Cl), was fully diastereoselective and gave the pure trans-13 with inversion of configuration. In this connection, it is interesting to mention that the condensation reactions of isomeric cisand trans-chlorides and bromides, 6(Cl) and 6(Br) with the diastereomeric thioacid 9 anions occurred almost exclusively by inversion of P-configuration [24].
Before discussing our present results on displacement reactions in the diastereomeric thiophosphoryl fluorides 6(F), it is necessary to note that Inch and coworkers [30] reported very early that the displacement of fluorine by nucleophilic reagents in the 1,3,2dioxaphosphorinan-2-ones derived from carbohydrates occurs with preponderant retention at phosphorus. However, the stereochemical course of these reactions was examined with only one, more stable diastereomer with the axial fluorine. Therefore, the discussion on the stereochemistry-mechanism relationship was rather limited and not conclusive. As we have been successful in preparing and purifying both cisand trans-fluorides 6(F), we decided to concentrate our attention on their alkaline hydrolysis. In the first place, this reaction was investigated with the thermodynamically more stable thiophosphoryl fluoride cis-6(F), and also with the axial fluorine, to compare our results with those reported by Inch. Thus, hydrolysis was carried out according to a general procedure also applied for other thiophosphoryl halogenides 6 (NaOH, H 2 O-dioxane, 0 • C) and resulted in a mixture of the two sodium salts of the thioacid cis-9 and trans-9 in a ratio of 66:34 as estimated by 31 P-NMR spectra [27] (see Scheme 17). Similar results were obtained with the thiophosphoryl bromide trans-6(Br), which was used as a substrate in the three substitution reactions investigated herein (see Scheme 14). Thus, alkaline hydrolysis and methanolysis of this bromide were found to occur with a predominant inversion of configuration at phosphorus while aminolysis, as in the case of the trans-chloride 6(Cl), was fully diastereoselective and gave the pure trans-13 with inversion of configuration. In this connection, it is interesting to mention that the condensation reactions of isomeric cis-and trans-chlorides and bromides, 6(Cl) and 6(Br) with the diastereomeric thioacid 9 anions occurred almost exclusively by inversion of P-configuration [24].
Before discussing our present results on displacement reactions in the diastereomeric thiophosphoryl fluorides 6(F), it is necessary to note that Inch and coworkers [30] reported very early that the displacement of fluorine by nucleophilic reagents in the 1,3,2-dioxaphosphorinan-2-ones derived from carbohydrates occurs with preponderant retention at phosphorus. However, the stereochemical course of these reactions was examined with only one, more stable diastereomer with the axial fluorine. Therefore, the discussion on the stereochemistry-mechanism relationship was rather limited and not conclusive. As we have been successful in preparing and purifying both cis-and trans-fluorides 6(F), we decided to concentrate our attention on their alkaline hydrolysis. In the first place, this reaction was investigated with the thermodynamically more stable thiophosphoryl fluoride cis-6(F), and also with the axial fluorine, to compare our results with those reported by Inch. Thus, hydrolysis was carried out according to a general procedure also applied for other thiophosphoryl halogenides 6 (NaOH, H2O-dioxane, 0 °C) and resulted in a mixture of the two sodium salts of the thioacid cis-9 and trans-9 in a ratio of 66:34 as estimated by 31 P-NMR spectra [27] (see Scheme 17). This result clearly showed that the fluoride cis-6(F) underwent hydrolytic conversion to cis-9(Na) as the major product with retention of configuration at phosphorus. In this way, the results of Inch were to some extent corroborated. However, the most intriguing was a high content of the sodium salt of trans-9, which was simultaneously formed in this reaction with inversion of configuration, as epimerization of the more stable cis-6(F) to its less stable trans-isomer does not occur in the presence of fluoride anion. Such a stereo- This result clearly showed that the fluoride cis-6(F) underwent hydrolytic conversion to cis-9(Na) as the major product with retention of configuration at phosphorus. In this way, the results of Inch were to some extent corroborated. However, the most intriguing was a high content of the sodium salt of trans-9, which was simultaneously formed in this reaction with inversion of configuration, as epimerization of the more stable cis-6(F) to its less stable trans-isomer does not occur in the presence of fluoride anion. Such a stereochemical outcome of alkaline hydrolysis should be due to a different mechanism of hydrolysis of 2-fluorophosphorinanes 6(F) as compared with their chloro-and bromoanalogues. We have also noted a negligible effect of the reaction medium and added inorganic salts on the retention-inversion ratio (see Table 2). Table 2. Effect of reaction medium on percentage of cisand trans-isomers of thioacid 9 obtained in hydrolysis of thiophosphoryl fluoride cis-6(F).

No Reaction Medium
Sodium Salt The results of alkaline hydrolysis of the less stable fluoride trans-6(F) (equatorial fluorine) were even more interesting. In this case, two sodium salts of the thioacid 9 were obtained in a 73:27 ratio; however, the major product, cis-9(Na), was formed with inversion of configuration (see Scheme 18). The results of alkaline hydrolysis of the less stable fluoride trans-6(F) (equatorial fluorine) were even more interesting. In this case, two sodium salts of the thioacid 9 were obtained in a 73:27 ratio; however, the major product, cis-9(Na), was formed with inversion of configuration (see Scheme 18). In additional experiments, it was found that diastereomeric purity of the starting thiophosphoryl fluoride trans-6(F) has practically no effect on the product ratio, which is in this case equivalent to the inversion-retention ratio (see Table 3). Table 3. Effect of diastereomeric purity of thiophosphoryl fluoride trans-6(F) on percentage of cisand trans-isomers of thioacid 9 sodium salt.

No
Diastereomeric Purity of trans-6(F), dp (%) 1  71  78  22  2  89  77  25  3  90  74  26  4  94  73  27 To estimate the effect of epimerization of the starting trans-fluoride 6(F) to cis-isomer by fluoride ion, alkaline hydrolysis was performed with an insufficient molar amount of sodium hydroxide. The results obtained are shown in Scheme 19. It turned out that the unreacted fluoride trans-6(F) was only slightly epimerized and recovered with 84% diastereomeric purity. Therefore, this side process considered here cannot essentially change the main stereochemical outcome of hydrolysis. In additional experiments, it was found that diastereomeric purity of the starting thiophosphoryl fluoride trans-6(F) has practically no effect on the product ratio, which is in this case equivalent to the inversion-retention ratio (see Table 3). Table 3. Effect of diastereomeric purity of thiophosphoryl fluoride trans-6(F) on percentage of cisand trans-isomers of thioacid 9 sodium salt.

No
Diastereomeric Purity of trans-6(F), dp (%) 1  71  78  22  2  89  77  25  3  90  74  26  4  94  73  27 To estimate the effect of epimerization of the starting trans-fluoride 6(F) to cis-isomer by fluoride ion, alkaline hydrolysis was performed with an insufficient molar amount of sodium hydroxide. The results obtained are shown in Scheme 19. It turned out that the unreacted fluoride trans-6(F) was only slightly epimerized and recovered with 84% diastereomeric purity. Therefore, this side process considered here cannot essentially change the main stereochemical outcome of hydrolysis.

trans-9(Na) (%) Retention
To estimate the effect of epimerization of the starting trans-fluoride 6(F) to cis-isomer by fluoride ion, alkaline hydrolysis was performed with an insufficient molar amount of sodium hydroxide. The results obtained are shown in Scheme 19. It turned out that the unreacted fluoride trans-6(F) was only slightly epimerized and recovered with 84% diastereomeric purity. Therefore, this side process considered here cannot essentially change the main stereochemical outcome of hydrolysis. Scheme 19. Partial alkaline hydrolysis of thiophosphoryl fluoride trans-6(F).
Finally, for comparison purposes, the reaction of the more stable thiophosphoryl fluoride cis-6(F) with sodium methoxide was briefly investigated. In accord with the results of alkaline hydrolysis of this thiofluoridate, its methanolysis afforded both isomeric thionophosphatescis-12 and trans-12, the former being the major product was formed with retention of configuration as shown in Scheme 20. Finally, for comparison purposes, the reaction of the more stable thiophosphoryl fluoride cis-6(F) with sodium methoxide was briefly investigated. In accord with the results of alkaline hydrolysis of this thiofluoridate, its methanolysis afforded both isomeric thionophosphatescis-12 and trans-12, the former being the major product was formed with retention of configuration as shown in Scheme 20. It was also found that the product isomer ratios are practically not influenced by solvents, both protic and aprotic, indicating that they reflect the mode of substitution (Table  4). Table 4. Effects of solvents on percentage of cis-and trans-thiophosphates 12 obtained in methanolysis of thiophosphoryl fluoride cis-6(F). Dissecting the results of our studies on the stereochemistry of displacement reactions at phosphorus in 2-halogeno-4-methyl-1,3,2-dioxaphosphorinan-2-thiones 6 presented above several important observations and interpretations can be inferred. First of all, there is a sharp difference in the stereochemical course of substitution reactions between diastereomeric thiophosphoryl chlorides and bromides 6(Cl, Br) on the one side and fluorides 6(F) on the other side. Both diastereomeric chlorides 6(Cl) and bromides 6(Br) react with nucleophilic reagents as a rule with full inversion of configuration at phosphorus. A small decrease of diastereoselectivity observed in alkaline hydrolysis and methanolysis is due to concomitant side epimerization reactions of a substrate and/or a product of the displacement reaction investigated. In the case of thiophosphoryl chlorides 6(Cl) and bromides 6(Br), the substitutions are kinetically controlled, which implies that inversion at phosphorus may be a consequence of a direct SN2-P type displacement.

No. Solvent
In contrast to the diastereomeric chlorides 6(Cl), both diastereomeric fluorides (cis-6(F) and trans-6(F)) undergo alkaline hydrolysis, affording the same mixture of the corresponding thioacids 9 with the thermodynamically more stable thioacid cis-9 being a major product in both cases. It means that hydrolysis of cis-6(F) affords cis-9 with retention of configuration, while trans-6(F) upon hydrolysis gives the same major product with inversion of configuration. Such a stereochemical outcome of alkaline hydrolysis of both isomeric fluorides 6(F) and other observations presented above indicate that this reaction as well as methanolysis are controlled by thermodynamic factors. Taking into account well known facts that (a) fluorine forms a very strong bond with phosphorus, (b) the fluoride anion is a poor leaving group, and (c) fluorine as a substituent stabilizes pentacoordinate phosphorus and is strongly apicophilic, it is believed that nucleophilic substitution at phosphorus in thiophosphoryl fluorides 6(F) occurs according to the addition-elimination It was also found that the product isomer ratios are practically not influenced by solvents, both protic and aprotic, indicating that they reflect the mode of substitution (Table 4). Table 4. Effects of solvents on percentage of cisand trans-thiophosphates 12 obtained in methanolysis of thiophosphoryl fluoride cis-6(F).

Thionophosphate 12
cis-12 trans-12 Dissecting the results of our studies on the stereochemistry of displacement reactions at phosphorus in 2-halogeno-4-methyl-1,3,2-dioxaphosphorinan-2-thiones 6 presented above several important observations and interpretations can be inferred. First of all, there is a sharp difference in the stereochemical course of substitution reactions between diastereomeric thiophosphoryl chlorides and bromides 6(Cl, Br) on the one side and fluorides 6(F) on the other side. Both diastereomeric chlorides 6(Cl) and bromides 6(Br) react with nucleophilic reagents as a rule with full inversion of configuration at phosphorus. A small decrease of diastereoselectivity observed in alkaline hydrolysis and methanolysis is due to concomitant side epimerization reactions of a substrate and/or a product of the displacement reaction investigated. In the case of thiophosphoryl chlorides 6(Cl) and bromides 6(Br), the substitutions are kinetically controlled, which implies that inversion at phosphorus may be a consequence of a direct S N 2-P type displacement.
In contrast to the diastereomeric chlorides 6(Cl), both diastereomeric fluorides (cis-6(F) and trans-6(F)) undergo alkaline hydrolysis, affording the same mixture of the corresponding thioacids 9 with the thermodynamically more stable thioacid cis-9 being a major product in both cases. It means that hydrolysis of cis-6(F) affords cis-9 with retention of configuration, while trans-6(F) upon hydrolysis gives the same major product with inversion of configuration. Such a stereochemical outcome of alkaline hydrolysis of both isomeric fluorides 6(F) and other observations presented above indicate that this reaction as well as methanolysis are controlled by thermodynamic factors. Taking into account well known facts that (a) fluorine forms a very strong bond with phosphorus, (b) the fluoride anion is a poor leaving group, and (c) fluorine as a substituent stabilizes pentacoordinate phosphorus and is strongly apicophilic, it is believed that nucleophilic substitution at phosphorus in thiophosphoryl fluorides 6(F) occurs according to the addition-elimination (A-E) mechanism.
To calculate the energy of this substitution reaction, we first performed conformational analysis of reagents (6(Cl), 6(F)) and the product, 2-hydroxy-4-methyl-1,3,2dioxaphosphorinan-2-thione 9. In the case discussed here, the presence of the methyl group at C 4 in the six-membered ring induces stereoisomerism in the molecule, which may result in a different reactivity of diastereomers towards the nucleophile. Therefore, we calculated chair and boat conformations for both cisand transdiastereomers of chlorides 6(Cl) and fluorides 6(F) and compared the Gibbs free energies of all stable minima.
The most stable diastereomer of 6(Cl) was found to exist in a chair conformation with chlorine in the axial position and methyl in the equatorial position, denoted in this work as trans-6(Cl). The remaining conformers are ∆G rel = 2.5-5.6 kcal/mol higher in energy than trans-6(Cl). The relative Gibbs free energies of all isomers are collected in Table S1. These data show a strong preference for chlorine to the axial position. All isomers with chlorine occupying the equatorial position have much higher energies. Additional stabilization of trans-6(Cl) is due to the methyl group in equatorial arrangement, which minimizes the steric congestion. These observations support the common knowledge about these ring systems [10].
The stability order of conformers of 6(F) is very similar in terms of relative stereochemistry. One should remember that due to the different priority of substituents, upon replacement of Cl for F, the most stable conformation is again that with axial fluorine and an equatorial methyl group, i.e., cis-6(F) (see Supplementary Materials, Table S2 and Figure S2). Comparison of the calculated structure of this isomer in the aqueous solution agrees very well with the reported crystal structure [28], which proves the reliability of the theoretical method used (Supplementary Materials, Table S4).
The most stable conformer of 9 is that with the axial hydroxyl and equatorial C 4methyl group, i.e., cis-9, as in the case of fluorine and chlorine. However, only slightly less stable (by 0.7 kcal/mol) is the isomer trans-9 with both hydroxyl and methyl groups in equatorial positions (Supplementary Materials, Table S3 and Figure S3).
DFT calculations of the alkaline hydrolysis of trans-6(Cl) in water showed that indeed the preferred reaction route is the attack of hydroxide ion from the opposite side to chlorine and the ligand exchange occurs with inversion of configuration. It is a one-step reaction that proceeds via a single transition state as was found for acyclic alkoxyphosphoryl chlorides [35,36]. Both trans and cis isomers react according to the same S N 2-P mechanism and their free energy profiles are almost identical ( Figure 6). The analogous hydrolysis of 6(F) seems more complicated in view of the experimental results. To deeper understand the mechanistic and stereochemical details of this process, we performed analogous DFT calculations of the replacement of fluoride ion in cis-and trans-6(F) by hydroxyl anion in water solution. Anticipating that the reaction may occur stepwise according to the addition-elimination scheme [35], we considered at first the reaction pathways starting from the approach of the nucleophile to each face of the tetrahedron formed by S, O(C4), O(C6), and F (Scheme 21). The stationary points on the reaction pathway (intermediates and transition states) were identified by computing potential energy scans (PES) of the reaction. The route (a) should lead to formation of a trigonal bipyramidal intermediate (TBPI) with OH and F in apical positions. The route (b) consists of two directions of nucleophilic attack, from the opposite side relative to each oxygen in the ring. Energetically, both routes (b-1 and b-2) are almost equivalent. The The analogous hydrolysis of 6(F) seems more complicated in view of the experimental results. To deeper understand the mechanistic and stereochemical details of this process, we performed analogous DFT calculations of the replacement of fluoride ion in cisand trans-6(F) by hydroxyl anion in water solution. Anticipating that the reaction may occur stepwise according to the addition-elimination scheme [35], we considered at first the reaction pathways starting from the approach of the nucleophile to each face of the tetrahedron It should be mentioned that the frontside attack, although usually associated with a much higher energy barrier than the backside attack [37], is in this case possible as it leads to the TBPI with electronegative oxygen in the apical position. Moreover, the ring in such TBPI occupies the apical-equatorial position, which is the preferred arrangement in terms of the ring strain. In contrast to chloride substitution, it was found that all reaction routes involving fluoride 6(F) proceed via pentacoordinate intermediates, as suggested by stereochemical studies (taking into account the high electronegativity and apicophilicity of fluorine). Below, all P V intermediate structures identified for reaction pathways (a)-(c) of cis and trans diastereomers of 6(F) are presented in Figures 7 and 8).  It should be mentioned that the frontside attack, although usually associated with a much higher energy barrier than the backside attack [37], is in this case possible as it leads to the TBPI with electronegative oxygen in the apical position. Moreover, the ring in such TBPI occupies the apical-equatorial position, which is the preferred arrangement in terms of the ring strain. In contrast to chloride substitution, it was found that all reaction routes involving fluoride 6(F) proceed via pentacoordinate intermediates, as suggested by stereochemical studies (taking into account the high electronegativity and apicophilicity of fluorine). Below, all P V intermediate structures identified for reaction pathways (a)-(c) of cis and trans diastereomers of 6(F) are presented in Figures 7 and 8). It should be mentioned that the frontside attack, although usually associated with a much higher energy barrier than the backside attack [37], is in this case possible as it leads to the TBPI with electronegative oxygen in the apical position. Moreover, the ring in such TBPI occupies the apical-equatorial position, which is the preferred arrangement in terms of the ring strain. In contrast to chloride substitution, it was found that all reaction routes involving fluoride 6(F) proceed via pentacoordinate intermediates, as suggested by stereochemical studies (taking into account the high electronegativity and apicophilicity of fluorine). Below, all P V intermediate structures identified for reaction pathways (a)-(c) of cis and trans diastereomers of 6(F) are presented in Figures 7 and 8). The lowest free energy barrier in the case of cis-6(F) is associated with the classical backside attack of hydroxyl relative to fluorine (path a). The side attack (b), which places the ring in apical-equatorial position, has the barrier by ca. 1 kcal/mol higher ( Table 5). The approach of OH − from the back direction relative to sulfur is associated with the highest free energy barrier (by 8 kcal/mol higher than (a)), so it is the least likely. However, calculations showed that this pathway leads to the most stable TBPI, which also loses fluoride most readily to give the thioacid 9, as can be seen in Supplementary Materials, Figure S7. Thus, from the kinetic point of view, the formation of intermediate (a) seems preferable. Most probably, the pentacoordinate intermediate formed as a result of backside attack (a) can undergo a sequence of reversible pseudorotations, eventually leading to a major product with retention of configuration on P, in accord with thermodynamic equilibrium [38]. Indeed, we have identified at least one sequence of pseudorotations linking both intermediates 6(F)-a and 6(F)-c (Scheme 14).  The lowest free energy barrier in the case of cis-6(F) is associated with the classical backside attack of hydroxyl relative to fluorine (path a). The side attack (b), which places the ring in apical-equatorial position, has the barrier by ca. 1 kcal/mol higher ( Table 5). The approach of OH − from the back direction relative to sulfur is associated with the highest free energy barrier (by 8 kcal/mol higher than (a)), so it is the least likely. However, calculations showed that this pathway leads to the most stable TBPI, which also loses fluoride most readily to give the thioacid 9, as can be seen in Supplementary Materials, Figure S7. Thus, from the kinetic point of view, the formation of intermediate (a) seems preferable. Most probably, the pentacoordinate intermediate formed as a result of backside attack (a) can undergo a sequence of reversible pseudorotations, eventually leading to a major product with retention of configuration on P, in accord with thermodynamic equilibrium [38]. Indeed, we have identified at least one sequence of pseudorotations linking both intermediates 6(F)-a and 6(F)-c (Scheme 14). The reactivity of the diastereomer trans-6(F) is somewhat different. The attack of OH − from the opposite side to fluoride (a) has the lowest free energy barrier (by 7 kcal/mol lower than the attack (b)). The attack from the opposite side to sulfur (c) is again the most unfavourable. This suggests that the reaction with inversion of configuration should kinetically dominate, which is in accord with observations. The thermodynamic parameters of hydrolysis of both diastereomers are presented in Tables 5 and 6 and the free energy profiles for routes (a) and (b) of cisand trans-6(F) hydrolysis are compared in Figure 9. The difference in energies of the free products comes from the fact that in route (a) the free fluoride anion is formally produced as the byproduct while in routes (b) and (c) it is HF and thiophosphate anion. The reaction leading to hydrogen fluoride and thiophosphate anion is much more favourable thermodynamically but in alkaline medium; this of course is meaningless as the fast equilibrium between these species is immediately established.    The DFT calculations presented above provided convincing evidence that alkaline hydrolysis of cyclic thiophosphoryl fluorides 6(F) proceeds according to the addition-  (Tables 5 and 6).
The DFT calculations presented above provided convincing evidence that alkaline hydrolysis of cyclic thiophosphoryl fluorides 6(F) proceeds according to the additionelimination mechanism (A-E) and allowed us to rationalize the stereochemical course and thermodynamic control of this reaction. Taking into account the Westheimer's rules (apical attack, apical departure, pseudorotation, microscopic reversibility), we formulated the most likely mechanism of the alkaline hydrolysis of fluorophosphorinans, which is presented in Scheme 22. Thus, the attack of a hydroxyl anion on phosphorus in cis-6(F) results in formation of the first trigonal bipyramidal intermediate TBPI-A with apical fluorine and OH group and diequatorial six-membered ring. It decomposes slowly with inversion of configuration to thioacid trans-9, which is the minor product of this reaction. The fast Berry pseudorotation of TBPI-A leads to TBPI-B, which, in turn, undergoes permutational isomerization to TBPI-C and TBPI-D. Decomposition of the latter by departure of HF is virtually barrierless (see Supplementary Materials, Figure S7) and leads to the thermodynamically more stable thioacid cis-9 with retention of configuration. This thioacid is the major and stable product. In the case of hydrolysis of trans-6(F), the more stable thioacid cis-9 is formed from the first TBPI-A' with inversion of configuration. The thioacid trans-9 as the minor product of hydrolysis is formed after three consecutive pseudorotations with retention of P-configuration. As the phosphorane intermediate TBPI-B (and TBPI-B') with the apical S are energetically unstable and could not be localized, it is possible that the transformation of TBPI-A into TBPI-C can take place directly via the tetragonal pyramidal intermediate (which may be a 2nd order saddle point) transiently formed from TBPI-A in the process of pseudorotation. 9 as the minor product of hydrolysis is formed after three consecutive pseudor with retention of P-configuration. As the phosphorane intermediate TBPI-B (and with the apical S are energetically unstable and could not be localized, it is poss the transformation of TBPI-A into TBPI-C can take place directly via the tetrag ramidal intermediate (which may be a 2nd order saddle point) transiently form TBPI-A in the process of pseudorotation.

Scheme 22.
Mechanism of alkaline hydrolysis of cis-6(F) and trans-6(F) (bold arrows show mation of major product cis-9 from cis and trans fluorides).

General Experimental Details
Scheme 22. Mechanism of alkaline hydrolysis of cis-6(F) and trans-6(F) (bold arrows show formation of major product cis-9 from cis and trans fluorides).

General Experimental Details
Commercial grade reagents and solvents were used without further purification except as indicated below. THF and diethyl ether were distilled over Na/benzophenone prior to use. Column chromatography was performed using silica gel (70-230 mesh). The routine 1 H-NMR spectra were recorded at 60 and 80 MHz unless stated otherwise. Chemical shifts are quoted in parts per million (ppm) and reported relative to TMS as an internal standard. 31 P-NMR spectra were obtained with a spectrometer operating at 24.3 MHz using 85% phosphoric acid as external standard. A heteronuclear spin decoupler was used for precise 31 P chemical shift determinations. Diastereomeric purities were determined from integrated 1 H-and 31 P-NMR spectra and GLPC analysis. Boiling and melting points are uncorrected.

Reaction of Cyclic Phosphorothioic Acid trans-9 with Phosphorus Pentachloride
To phosphorus pentachloride (1.04 g, 5 mmol) suspended in benzene (25 mL), thioacid trans-9 (0.84 g, 5 mmol) was added dropwise at 0-5 • C. The reaction mixture was stirred for 1 h at this temperature and for the next 1 h at room temperature. After removal of volatile reaction products, the residue was analysed by 31 P-NMR spectra. Based on the chemical shift values, intensity and shape of the P resonance signals, three compounds were identified as being the reaction products: 3.2.10. General Procedure for Methanolysis of 2-Halogeno-4-methyl-1,3,2-dioxaphosphorinan-2-thiones 6(Cl,Br,F) To a solution of sodium methoxide (0.069 g, 3 mmol Na, in methanol, 7 mL) in benzene (20 mL) (or CH 3 CN and DMF), cyclic thiophosphoryl halogenide 6 (3 mmol, 0.51, 0.56, 0.69 g for Cl, Br and F, respectively) was added at ca. 0 • C. The reaction mixture was stirred for an additional 2 h. Sodium halogenide that precipitated was removed by washing the reaction solution, and it was then dried and evaporated. The residue was analyzed by 31 P-NMR to determine the ratio of the diastereomeric methyl esters 12 formed (trans-12, δ P = 63.5 ppm, cis-12, δ P = 61.5 ppm). The pure esters 12 were obtained by distillation under reduced pressure. Methanolysis of trans-6(Cl) exemplifies the above general procedure.

Theoretical Methods
All quantum mechanical calculations were performed using the Gaussian 16 suite of programs [39]. Geometries of the model compounds were optimized using two DFT methods: the hybrid B3LYP density functional [40] corrected for dispersion interactions using Grimme GD3 empirical term [41], with the Def2TZVP basis set [42] in aqueous solution. SCRF calculations in water were performed using CPCM model with UFF atomic radii as implemented in Gaussian 16 [39]. All stationary points were identified as stable minima by frequency calculations. The vibrational analysis provided thermal enthalpy and entropy corrections at 298 K within the rigid rotor/harmonic oscillator/ideal gas approximation [39]. Thermochemical corrections were scaled by a factor of 0.99.

Data Availability Statement:
The data presented in this study are available on request from the corresponding author.