Heteroelement Analogues of Benzoxaborole and Related Ring Expanded Systems

Abstract

The review covers the chemistry of organoboron heterocycles structurally related to benzoxaboroles where one of the carbon atoms in a boracycle or a fused benzene ring is replaced by a heteroelement such as boron, silicon, tin, nitrogen, phosphorus, or iodine. Related ring expanded systems including those based on naphthalene and biphenyl cores are also described. The information on synthetic methodology as well as the basic structural and physicochemical characteristics of these emerging heterocycles is complemented by a presentation of their potential applications in organic synthesis and medicinal chemistry, the latter aspect being mostly focused on the promising antimicrobial activity of selected compounds.

1. Introduction

Recently, benzoxaboroles (Scheme 1, structure I) constitute one of the leading groups of organoboron compounds. This is mainly due to their promising biological properties, which have been exploited for the past 20 years in medicinal and bioanalytical chemistry [1,2,3,4]. Benzoxaboroles are strongly predestined for such applications due to their improved thermodynamic stability, resulting from the presence of a strong covalent boron-oxygen bond. Overall, they are rather stable to air and water and, in general, do not undergo rapid degradation under in vivo conditions. Therefore, heteroelement analogues of benzoxaboroles (Scheme 1, general structures II) constitute an interesting alternative and may offer the opportunity for various novel applications while retaining high stability arising from the presence of a strong B-O bond in the ring structure. The replacement of a carbon atom in the boracycle or an adjacent benzene ring with a different atom may result in a significant change of structural behaviour, e.g., a tendency to aggregation involving dative interactions of a heteroatom with the boron atom. Moreover, the presence of a heteroatom may result in modified physicochemical properties, including solubility, lipophilicity, hydrolytic stability, boron Lewis acidity, and others. The aim of this review is to highlight several emerging groups of boracyclic systems which comprise various heteroelement atoms such as another boron, silicon, tin, nitrogen, phosphorus, and iodine. Some ring expanded analogues (Scheme 1, general structures III), including compounds based on naphthalene and biphenyl-scaffold, are also included. Overall, the review is divided into sections based on type of heteroelement and heterocyclic ring as the primary and secondary classification criteria, respectively. The synthesis and physicochemical properties as well as applications of compounds of interest are consecutively presented in each section.

Scheme 1. Structures of benzoxaborole, I; its heteroelement congeners, II; and related ring-expanded systems, III. El stands for heteroatom or heteroatom-based fragment.

2. Benzoxadiboroles and Related Ring-Expanded Systems Comprising B-O-B Linkage

The formal substitution of the C3 carbon atom in benzoxaborole results in a benzoxadiborole framework featuring a B-O-B linkage within the five-membered ring. An example of such a well-defined boracyclic system (1) was reported by Kaufmann et al. in 1994 [5]. It was isolated in a low yield by aminolysis of 1,2-bis(dichloroboryl)benzene [6] followed by ring closure with hydroxide anion (Scheme 2).

Scheme 2. Synthesis of 1,3-bis(diisopropylamino)-1,3-dihydro-2,1,3-benzooxadiborole.

Phenylene-1,2-diboronic acid (2a) was found to be a useful precursor of benzooxadiborole derivatives (Scheme 3). It can be readily obtained by careful hydrolysis of 1,2-bis(dichloroboryl)benzene [6] or a Br/Li exchange reaction of 2-(2-bromophenyl)butyl[1,3,6,2]dioxazaborocan, followed by quenching the aryllithium intermediate with B(OMe)₃ (Scheme 3) [7]. Subsequent studies on the structural behaviour of 2 and its fluorinated derivatives (3–7) revealed that those compounds tend to equilibrate in solution with respective cyclic semi-anhydrides, i.e., 1,3-dihydroxy-1,3-dihydro-2,1,3-benzoxadiboroles (Scheme 3). ¹H and ¹³C NMR analyses in various dry deuterated solvents (acetone, THF, DMSO) revealed that cyclization (2a→2b) occurs to a significant extent. Moreover, the ¹¹B NMR spectrum showed that boron atoms (2) are slightly deshielded (by ca. 4 ppm) with respect to free acid. However, the B-O-B linkage is readily cleaved upon the addition of water (or D₂O), shifting the equilibrium towards free acid (2b).

Scheme 3. Synthesis of phenylene-1,2-diboronic acid (2a). Cyclization and acid-base equilibria involving 2a and 1,3-dihydroxybenzoxadiborole (2b).

The formation of 1,3-dihydroxybenzoxadiborole scaffold (2b) (Scheme 3) clearly accounts for the apparent stronger acidity (pK_a = 6.0) of the entire equilibrium system compared to related acyclic meta- and para-substituted phenylenediboronic acids [8,9]. Theoretical (DFT B3LYP) studies indicate that the relative stabilization the anionic form (2b-OH) is important in this respect, although the persistence of its hydrated forms, i.e., a cyclic species (2a-OH) with a bridging hydroxyl anion bound simultaneously by two boronic groups in a bidentate fashion and an unsymmetrical form (2a-OH′), stabilized by charge-assisted intramolecular H-bond, should also be taken into account.

Subsequent studies revealed that 3,4,5,6-tetrafluorophenylene-1,2-diboronic acid 7 shows a stronger tendency to intramolecular cyclization. X-ray diffraction analysis confirmed the formation of perfluorinated benzoxadiborole (7b), complexed with water molecules (Scheme 4) [8]. Interestingly, a unique dimeric form of 7c was also obtained by crystallization in toluene. The molecule consists of two benzoxadiborole frameworks fused by means of two B-OH-B bridges and additionally stabilized by π-π interactions of aromatic rings, resulting in a general chair-type conformation. Overall, the impact of perfluorination results in the strong acidity enhancement of 7 compared to 2, leading to an apparent pK_a of 3.0, which is among the lowest figures for boronic acids and related species.

Scheme 4. Structural diversity of 3,4,5,6-tetrafluorophenylene-1,2-diboronic acid (7) involving the standard open form (7a), the benzoxadiborole tautomer (7b) and the cyclic dimer (7c).

It was found that the benzoxadiborole scaffold is strongly stabilized upon treatment with -8-hydroxyquinoline (Scheme 5) [10]. The reactions of 2a/2b and its fluorinated derivatives 3–7 afforded respective chelate complexes 8–13, both in solution and under mechanochemical conditions. The most Lewis acidic 7 also bound readily two 8-oxyquinolinato ligands, yielding bis(chelate) (14) (Scheme 6) [10]. All of the obtained complexes exhibit green luminescence in acetonitrile solution (λ_em = ca. 525 nm, Φ = 13–15%), resembling other organoboron 8-oxyquinolinato complexes. Interestingly, it is blue-shifted in solid state (λ_em = ca. 500 nm), which was ascribed to the effect of H-bonding and other polar interactions of discrete molecules in the crystal lattice. Importantly, the electroluminescence properties of complexes 8 and 14 was proved by testing OLEDs containing those compounds as emitters [10]. Later on, complex 8 became the subject of in-depth structural characterization, which included interesting solvatomorphic behaviour [11] as well as high resolution single-crystal X-ray diffraction electron density studies performed for the first time in the case of a luminescent oxyquinolinato organoboron complex [12]. Furthermore, 2 was also employed for the synthesis of a series of luminescent (O,N)-chelate complexes (15–18) with 2-(imidazo[1,2-a]pyridin-2-yl)phenol ligands (Scheme 7) [13]. The products were also characterized by single crystal X-ray diffraction, which revealed formation of H-bonded dimers in the solid state.

Scheme 5. Synthesis of benzoxadiborole 8-oxyquinolinato complexes 8–13.

Scheme 6. Synthesis of benzoxadiborole bis(8-oxyquinolinato) complex 14.

Scheme 7. Synthesis of benzoxadiborole (O,N)-chelate complexes 15–18 with 2-(imidazo[1,2-a]pyridin-2-yl)phenol.

Transformations of strong bidentate Lewis acids of a general formula o-C6F4(BR2)2, R = C₆F₅ (19), and BR₂ = BC₁₂F₈ (20) gave rise to various anionic or neutral boracyclic species structurally closely related to 7b/7c (Scheme 8) [14,15,16,17]. However, it should be noted that most of them are formed, at least in a formal sense, by means of dative O→B interactions. Specifically, weakly-coordinating borate anions o-C6F4[B(C₆F₅)2]2(μ-OR), R = Me, Ph, C₆F₅, and C6F4[BC₁₂F₈]2(μ-OMe) were employed for stabilization of selected tertiary carbocations in respective ion-pair compounds (21–24 and 25, respectively) (Scheme 8) [15,16,17,18]. It was found that trityl salts (21–23) are effective co-catalysts of ethylene polymerization due to activation of dimethyl zirconocene (Cp₂ZrMe₂), resulting in corresponding products with Cp₂ZrMe⁺ cation [15,18]. Compound 21 was also used for generation of stannylium cationic species 26 (Scheme 9) [19].

Scheme 8. Synthesis of ion-pair compounds 21–25, comprising tertiary carbocations and weakly-coordinating anions based on perfluorinated benzoxadiborole backbones.

Scheme 9. Synthesis of stannylium cationic species 26.

The analogous oxonium salt with (Et₂O)₂H⁺ counterion was also obtained [19]. Similarly, related Bronsted acids based on solvated protons were generated from reactions of 19–20 with an excess of protic reagents (MeOH, H₂O) (Scheme 10) [20]. It should be noted that such species are generally prone to protolytic cleavage of B-C, which results in fragmentation of a boracyclic anions derived from 19. On the other hand, controlled treatment of 20 with MeOH/H₂O gives rise to various neutral species such as cyclic borinic ester (27) obtained upon protonolysis of one B-C bond in the borafluorene ligand, the unique system (28) with water molecule bridging two boron centres, water-coordinated borinic acid (29) as well as the benzoxadiborole (30) arising from the cleavage of another B-C bond. The molecular structures of compounds 27–30 were determined by X-ray diffraction. The studies on the reactivity of 19–20 towards water were directly connected to their use as potent initiators of isobutene polymerization. They were aimed at shedding light on the plausible role of dissolved water as a chain transfer agent in polymerizations involving 19–20 that give rise to weakly-coordinating counteranions. It was suggested that species featuring bridging water molecule such as compound 28 are active as a strong Brønsted acid that is able to protonate isobutene which initiates the polymer chain growth [20].

Scheme 10. Transformations of 20 to various boracyclic systems (27–30) upon interactions with MeOH and H₂O.

In addition, one can also mention herein the synthesis of a zwitterionic system (31) based on an anionic benzoxadiborole framework with a C₄-chain attached to an oxygen atom and decorated with a cationic phosphonium end group. This was obtained by the ring opening of the THF molecule due to interaction with a Frustrated Lewis Pair system composed of 1,2-bis(dichloroboryl)benzene and tris(tert-butyl)phosphine (Scheme 11) [21].

Scheme 11. Synthesis of a zwitterionic system 31 based on an anionic benzoxadiborole framework.

The ring-expanded benzoxadiborole analogues are based on naphthalene and biphenyl scaffolds. Thus, 1,3-dihydroxy-1H,3H-naphth[l,8-cd][l,2,6]oxadiborin (32) (Scheme 12) is easily accessible by diboronation of 1,8-dilithionaphthalene with B(OMe)₃ [22,23,24]; 4,9-Dimethoxy derivative (33) was obtained analogously and characterized by single-crystal X-ray diffraction [25]. Compound 32 was successfully used as a coupling partner in selected Suzuki–Miayura cross-coupling reactions, resulting in the formation of new aryl-aryl bonds [26,27,28]. Thus, its behaviour seems to be rather typical of arylboronic acids and their derivatives. However, unlike benzoxadiboroles, the B-O-B linkage in 32 seems to be rather stable as there are no data which might indicate that a reversible hydrolysis to naphthalene-1,8-diboronic acid occurs to any appreciable extent. Compound 32 was used as a starting material for synthesis of a few 1H,3H-naphth[l,8-cd][l,2,6]oxadiborin derivatives (34–37) where hydroxyl groups were replaced with OMe, Cl, Me [23], or mesityl (Mes) substituents [24], respectively.

Scheme 12. Synthesis of 1,3-dihydroxy-1H,3H-naphth[l,8-cd][l,2,6]oxadiborins (32–33) and conversion of 32 to 34–37.

Very recently, a structurally extended analogue of 32 based on bicyclohexene-peri-naphthalene framework 38 was obtained using an analogous protocol involving bromine-lithium exchange in an appropriate dibromide, followed by boronation. It should be stressed that the system features a significant ring strain arising from the presence of two C4 and one C5-ring fused with the naphthalene core. Nevertheless, 38 was used successfully for the synthesis of peri-substituted bis(hexyl ether) (39)via oxidation of B-C bonds followed by alkylation (Scheme 13) [29].

Scheme 13. Synthesis and transformation of a boracyclic system (38) featuring B-O-B linkage attached to bicyclohexene-peri-naphthalene scaffold.

Related oxadiborepins, i.e., 7-membered boracyclic systems comprising B-O-B linkage and 2,2′-biphenyl core, were also obtained [30,31,32]. It should be noted that the plausible equilibrium between biphenyl-2,2′-diboronic acid and its cyclic semi-anhydride (40) has not been studied to date, although its synthesis was reported already in 2002 [30], followed by crystallographic determination of 38 in 2011 [31]. Compounds 41–42 were obtained in a multistep protocol starting with 2,2′-dibromobiphenyl (Scheme 14). Remarkably, 41–42 were reported as efficient catalysts of dehydrative amidation of carboxylic acids with amine substrates. Initially, they were employed for efficient preparation of various α- and β-hydroxy substituted amides [32] but thereafter also proved effective in catalyzing the formation of Weinreb amides [33,34] as well as various oligopeptides [35]. In the former case, the proposed mechanism of the catalytic process involves the cooperation of the two boron atoms in 41–42, which enables the formation of a cyclic mixed anhydride with carboxylic acid molecule, as evidenced by the ESI MS spectrum; this is followed by an attack of amine on the activated carbonyl group (Scheme 15) [32]. It should be noted that the performance of 42 is impressive, as evidenced by low catalyst loading (even a 0.01 mol% turnover number (TON) parameter up to 7500).

Scheme 14. Synthesis of oxadiborepins 40–42.

Scheme 15. Direct amidation of β-hydroxy substituted carboxylic acids with amines in the presence of bromo-substituted oxadiborepins 41–42.

One can also mention the unexpected synthesis of the fused polycyclic oxadiborepin (44) from the diboraanthracene precusor (43) which involved double arylation with 8-bromo-1-naphthyllithium followed by successful debromination/C–C coupling using Ni(COD)₂/bpycatalyst (Scheme 16) [36]. The formation of a third C–C bond and the cleavage of two B–C bonds was observed when THF was used as the solvent. The ¹H NMR studies on the structural behaviour of 44 revealed that it exists in equilibrium with the respective diborinic acid (45) upon the addition of water, whereas complete conversion to the dibromo derivative (46) occurs upon heating with an excess of BBr₃. Compound 46 is readily reconverted back to 44 upon the addition of water.

Scheme 16. Synthesis and cleavage of the fused polycyclic oxadiborepin 44.

3. Benzosiloxaboroles and Related Ring-Expanded Systems Comprising B-O-Si Linkage

Benzosiloxaboroles are silicon analogues of benzoxaboroles where the carbon atom in a boracyclic ring is replaced by a silicon atom, thus resulting in the formation of a B-O-Si linkage. The first benzosiloxaborole derivative bearing mesityl group at the boron atom (49) was synthesized in 2008 (Scheme 17) [37,38]. The starting 1-dimesitylboryl-2-(dimethylsilyl) benzene (47) was subjected to hydrolysis of the Si-H bond followed by ring closure effected through an attack of silanol on one of the B-Mes bonds, yielding mesitylene as a byproduct. The reaction occurs slowly in THF at rt, but can be accelerated by heating or the addition of tertiary amine such as Et₃N and diazabicyclo[5.4.0]undec-7-ene (DBU). In the case of the latter, one can isolate an intermediate ionic compound (50) with the boracyclic anion resulting from the quantitative deprotonation of silanol (48). When heated in THF at 80 °C, it undergoes transformation to complex 51 with the DBU ligand coordinated to the boron atom in 49.

Scheme 17. Synthesis of benzosiloxaborole derivatives through intramolecular cleavage of B-C bond with SiOH group.

The bromine-lithium exchange reaction of ortho-(dimethylsilyl)bromobenzene with t-BuLi, followed by trapping with (isopropoxy)diarylboranes (52–53), resulted in borohydride intermediates (56–57), which form neutral ortho-(alkoxysilyl)(diarylboryl)benzenes (58–59) after the addition of chlorotrimethylsilane. The formation of 56–57 can be explained in terms of intramolecular hydride–isopropoxide exchange between silicon and boron atoms in initially formed unstable alkoxyborate complexes (54–55) (Scheme 18) [39].

Scheme 18. Synthesis of ortho-(alkoxysilyl) arylboranes (58–59) featuring dative Si-O(i-Pr)→B linkage.

Compound 58 reacts readily with MeOH and EtOH to give methoxysilane 60 and ethoxysilane 61, respectively (Scheme 19) [39]. The ¹¹B and ²⁹Si NMR spectroscopy data of 58–61 point to intramolecular O→B coordination, which results in the existence of cyclic structures. In addition, X-ray diffraction analysis of 60 confirmed the formation of a boracyclic ring involving a rather strong dative Si-O(Me)→B linkage (B-O distance of 1.652(2) Å). Remarkably, this interaction enhances reactivity of the Me-O bond owing to the enhanced electrophilic character of the carbon atom. Thus, the treatment of 60 with 1,4-diazabicyclo[2.2.2]octane (DABCO) afforded ionic complex 62, composed of silyloxyborate anion and DABCO-Me cation (Scheme 19). However, the oxygen atom in the anion is nucleophilic and can be readily methylated to regenerate 60. Finally, the cleavage of the Me-O bond in 60 can also be performed using KF in the presence of 18-crown-6 ligand to give potassium salt (63).

Scheme 19. Synthesis of ionic compounds 62–63, featuring benzosiloxaborolate anion.

Analogous ortho-(alkoxysilyl)(borafluorenyl)benzenes (64–65) were obtained using the protocol described above for 58–59. Compound 64 was readily converted to respective methoxy- and ethoxysilanes (66–67) and resulted in ionic compounds 68–69 upon treatment with 1,4-diazabicyclo[2.2.2]octane (DABCO) and KF/18-crown-6, respectively (Scheme 20) [40].

Scheme 20. Synthesis of ionic compounds 68–69 featuring benzosiloxaborolate anion comprising 9-borafluorenyl moiety.

The synthesis of a benzosiloxaboroles bearing hydroxy group at the boron atom, i.e., 3-hydroxybenzosiloxaboroles, was accomplished using two general protocols. The first one involves bromine-lithium exchange in ortho-bromoaryl(dimethyl)silanes and subsequent boronation with trialkyl borates B(OR)₃ (R = Me, Et, i-Pr), followed by hydrolysis, leading to intramolecular dehydrogenative condensation (Scheme 21) [41,42,43]. The second method involves the addition of Me₂Si(H)Cl to 2-(2-lithiophenyl)-butyl-1,3,6,2-dioxazaborocan or its functionalized analogue, generated via Br-Li exchange using n-BuLi in Et₂O/THF (1:1) at low temperatures, typically below −90 °C (Scheme 21) [41,42,43]. Extensive work resulted in the preparation of a number of 3-hydroxybenzosiloxaboroles (70–96) bearing substituents such as F, Cl, Br, CF₃, CN, CHO, CH₂OH, and B(OH)₂, attached at various positions of the aromatic ring [41,42,43].

Scheme 21. Synthesis of functionalized benzosiloxaborole derivatives.

The formation of 3-hydroxybenzosiloxaboroles was the subject of some mechanistic studies aimed mainly at the elucidation of the activation pathways of the Si-H bond in boronated arylsilane precursors. DFT (M06-2X22/6-31+G(d)23) theoretical calculations revealed that the process of ring closing is driven by the coordination of an oxygen atom from the B(OH)₂ or, far better, from the anionic B(OH)₃⁻ group to the silicon atom (Scheme 22) [44].

Scheme 22. The proposed mechanism for the activation of the Si–H bond by the anionic boronate group in the presence of water.

On the other hand, experimental studies showed that, in the absence of water, the ortho-(dimethylsilyl)-substituted trialkoxyaryl(boronate) anion undergoes hydride transfer from silicon to boron to give a mixture of tris(hydrido)arylborate and tris(alkoxy)arylborate anions (97–98) as confirmed by ¹¹B NMR spectroscopy data (Scheme 23) [43]. Hydrolysis of the mixture proceeds with hydrogen evolution, and the final intramolecular condensation of transiently generated silanol and boronic groups occurs readily to give the siloxaborole ring. In fact, DFT calculations indicate that this process is thermodynamic and favourable, to a similar extent, as the condensation of carbinol and boronic groups, resulting in the formation of B-O-C linkage in benzoxaboroles [41].

Scheme 23. Activation of the Si–H bond by the anionic trialkoxyboronate group through hydride-alkoxy exchange between silicon and boron [41].

It was found that the activated Si-H bond was able to reduce nitrile to the formyl group, which was used for synthesis of compound 86 (Scheme 24) [42].

Scheme 24. Activation of the Si–H bond by the anionic trialkoxyboronate group, resulting in reduction of the nitrile group and formation of (86).

Interestingly, the reduction of otherwise rather inert acetal CH(OMe)₂ groups was observed, giving rise to benzosiloxaboroles comprising an additional fused oxaborole ring (99 and 100) (Scheme 25) [42]. An analogous system (101) with two siloxaborole heterocycles fused with the central aromatic ring was also prepared using a double Br-Li exchange in appropriate bis(dimethylsilyl)dibromobenzene, followed by boronation (Scheme 26) [43].

Scheme 25. Synthesis of 99–100 involving the reduction of acetal CH(OMe)₂ group with activated Si–H bond.

Scheme 26. Synthesis of benzobis(siloxaborole) 101.

It should be noted that formyl-substituted benzosiloxaboroles (87–89) are cleanly reduced to respective carbinol derivatives (91–93) using NaBH₄, whilst an analogous reaction of 90 afforded a unique dimeric species (102) featuring a central 10-membered heterocycle comprising two B-O-Si linkages. Its formation is apparently driven by the preferred formation of an oxaborole ring with concomitant breakdown of the siloxaborole ring with the release of free silanol moiety. Subsequent bimolecular dehydrative condensation leads to the formation of 102 (Scheme 27) [42].

Scheme 27. Synthesis of extended borasiloxane heterocycle system (102) through the reduction of 89.

In addition, a formyl derivative (89) was successfully subjected to reductive amination with dopamine, giving rise to the benzosiloxaborole conjugate (103) (Scheme 28) [42].

Scheme 28. Reductive amination of (89) leading to dopamine conjugate (103).

Very recently, the 6-hydroxy-7-chloro substituted 3,3-difluorobenzosiloxaborolate anion was prepared in the form of a potassium salt (110), starting with the protection of 4-bromo-2-chlorophenol (105) with tert-butylsilyldimethyl chloride (TBDMS-Cl), followed by introduction of the Si(H)Me₂ group, subsequent boronation, and cleavage of the silyl ether group (OTBDMS) in benzosiloxaborole (107) (Scheme 29) [45]. Similar reactions were performed using 4-bromo-2-fluorophenol (104) as the starting material. Unfortunately, the final cleavage of the OTBDMS group in 106 resulted in a mixture containing a significant amount of aryltrifluoroborate salt (108), together with the desired boracyclic species (109), which hampered further applications.

Scheme 29. Synthesis of potassium hydroxy-substituted benzosiloxa(difluoro)borolates 109–110.

The salt (110) was used as a phenolate O-nucleophile for reactions with MeI, Et₂NCOCl, benzoyl, and benzenesulfonyl chlorides as electrophilic partners. The syntheses proceeded smoothly under mild conditions, giving rise to a series of functionalized benzosiloxaboroles (111–137), respectively (Scheme 30) [45].

Scheme 30. Synthesis of functionalized benzosiloxaboroles 111–137.

Structurally closely related 6-(chloropyridinyl-2-oxy)-7-fluorobenzosiloxaboroles (138–139) were also obtained using a standard protocol (Scheme 31) [45].

Scheme 31. Synthesis of functionalized benzosiloxaboroles (138–139).

In addition, it is worth noting that Br-Li exchange in arylsilane (140), followed by treatment with B(Oi-Pr)₃ (0.5 equiv) gave selectively a unique borinate-type species (141) in ca. 70% yield (Scheme 32) [44]. The X-ray diffraction analysis revealed that its molecular structure features the spiro-arrangement of a central boron atom, linking two benzosiloxaborole systems. In crystal structure, discrete molecules form centrosymmetric dimers due to strong and symmetrical hydrogen bonds (O⋯O distance is only 2.432 Å). VT NMR analyses point to a dynamic character of 141 in CDCl₃ solution. Remarkably, acetone-d₆ (141) undergoes rearrangement to form 8-membered heterocyclic borinic acid (142) comprising the Si–O–Si linkage. However, the process is reversible because crystallization again afforded 141, whilst prolonged exposure of the solution to air (>1 week) resulted in extensive degradation.

Scheme 32. Synthesis and reversible rearrangement of spiro-borinate species 141.

X-ray diffraction analyses of selected benzosiloxaboroles showed that their molecular structures are similar to those found for related benzoxaboroles. This is also true for supramolecular assembly, which is typically based on centrosymmetric H-bonded dimers [41,45]. Determination of the acidity of selected derivatives in water/methanol solution revealed that their pK_a values vary in a wide range (~4.0–8.0), depending on substitution pattern [43,45]. 1,1-Dimethyl-3-hydroxybenzosiloxaborole (70) is a stronger acid (pK_a = 7.9) than its benzoxaborole counterpart (pK_a = 8.3) [41]. Increased acidity of the boron atom in 70 arises apparently from its lower saturation by the endocyclic oxygen lone pairs owing to competition with distinctive Si-O bond conjugation (back-bonding effect). In addition, it was observed that the presence of more electron-withdrawing phenyl groups at the silicon atom increases the acidity in comparison to SiMe₂ derivatives. In combination with perfluorination of the benzene ring, this resulted in the highest acidity of benzosiloxaborole (77) (pK_a = 4.2) among all of the studied derivatives. Notably, the acidity of borinate species (141) is even higher (pK_a = 3.5) [44] and very strongly enhanced with respect to the related simple 7-fluorobenzosiloxaborole (72) (pK_a = 7.2).

Selected functionalized 3-hydroxybenzosiloxaboroles emerged as novel small-molecule therapeutic agents. Simple halogenated derivatives (72–80) exhibit good antifungal activity with low Minimal Inhibitory Concentration (MIC) values (0.78–12.5 mg/L) for strains from Candida genus such as C. albicans, C. tropicalis, C. krusei, and C. guilliermondii. Thus, they can be regarded as effective silicon bioisosteres of related benzoxaboroles such as 5-fluorobenzoxaborole (Tavaborole), which has already been approved for the use against onychomycosis of the toenails [4].

Benzosiloxaboroles (70–139) were also screened as potential antibacterial agents against selected Gram-positive and Gram-negative strains. Overall, they showed at best a weak activity against Gram-negative bacilli, which was ascribed to the effective extrusion of used agents through bacterial walls by MDR efflux pumps. The highest increase in bacterial susceptibility to benzosiloxaboroles in the presence of efflux-pump inhibitor PAβN was observed for chloro derivatives (79-80) as MIC values decreased from 400 mg/L to 6.25 mg/L for E. coli and from 100–200 mg/L to 6.25 mg/L for S. maltophilia [43].

Benzosiloxaboroles show strongly varying activity against Gram-positive bacteria. The most promising results were obtained with respect to selected cocci strains such as Staphylococcus aureus (including MRSA strains), S. epidermidis, Enterococcus faecalis, and E. faecium, with MICs in the range of 6.25–50 mg/L in some cases. Interestingly, replacement of the fluoro substituent with the chloro one has the positive impact effect on the activity against Gram-positive cocci [43]. 6-Arylsulfonyloxy-7-chloro benzosiloxaboroles (113–130) showed high activity towards S. aureus species, including methicillin-resistant strains, with low MIC values in the range of 0.39–3.12 mg/L. Compounds 123, 129, and 130 also showed relatively high activity against other Gram-positive cocci such as E. faecalis and E. faecium, with MIC value of 6.25 mg/L. It should be noted that related 6-benzoyloxy derivatives (131–137) showed only moderate or weak activity against Gram-positive bacteria (MIC range = 12.5–400 mg/L), which indicates that benzenesulfonyl moiety is necessary to achieve high activity against studied cocci [45].

Benzosiloxaboroles (70–96) were also subjected to studies on inhibition of β-lactamases KPC- and pAmpC-produced by Gram-negative rods. Those enzymes provide multi-resistance to β-lactam antibiotics such as penicillins, cephalosporins, cephamycins, and carbapenems. Compounds 75, 76, 99 and, especially, 6-B(OH)₂-substituted derivative (95) showed promising inhibitory activity. It should be noted that they were essentially inactive (MICs > 400 mg/L) against the studied Gram-negative strains when used alone but showed high activity when combined with meropenem. Molecular modelling studies confirmed strong inhibitory activity of those compounds with respect to KPC-2 carbapenemase [43].

The studies on antimicrobial activity of benzosiloxaboroles were complemented by evaluation of their cytotoxicity towards normal human lung fibroblasts MRC-5. It is worth noting that most of the studied compounds presented rather weak cytotoxicity or can be regarded as essentially non-toxic, which increases their potential in medicinal chemistry [43,45].

In addition, fluorinated 3-hydroxybenzosiloxaborole derivatives (72,74, and 76) showed superior binding properties towards biologically-relevant diols in neutral pH aqueous conditions. Association constants K_s with dopamine, ribose, glucose, fructose, sorbitol, and adenosine and its monophosphate (AMP) were determined using the Springsteen and Wang method, with ARS as a fluorescent probe [41]. Later on, compounds 72, 75, 76, 96, and 102 were employed for the chemometric differential fluorescence-based sensing of saccharides such as glucose, fructose, ribose, sorbitol, lactose, and sucrose [46].

The synthesis and use of ring-expanded analogues of benzosiloxaboroles is currently at the initial stage of development. In 2018, Hartwig et al. obtained 1,1-dimethyloxasilaborinin-3-ol (145), comprising B-O-Si moiety bridging peri-naphthalene scaffold via Ir(I)-catalyzed CH-borylation of 1-(dimethylsilyl)naphthalene (143), followed by hydrolytic cleavage of intermediate pinacol boronate (144) in the presence of a Ru(II) catalyst. (Scheme 33) [47].

Scheme 33. Synthesis of 1,1-dimethyloxasilaborinin-3-ol (145).

Compound 145 was tested as a starting material for further transformations based on conversion of the B-C bond, including synthesis of a biaryl (146) by Suzuki–Miyaura cross coupling reaction, copper-mediated/catalyzed halogenation, and azide formation, as well as oxidation with meta-chloroperbenzoic acid (mCPBA), leading to the formation of naphthalene-fused oxasilole (147). Oxidation of both C-B and C-Si bonds was performed using an excess of H₂O₂ under basic conditions to give naphthalene-1,8-diol (148) (Scheme 34) [47].

Scheme 34. Transformations of 145 involving B-C bond activation.

Borylated indole (149) was obtained by a similar catalytic method reported for the synthesis of 143 (Scheme 35) [48]. A subsequent reaction with aq. H₂O₂ afforded indole-based oxasilaborininol (150) instead of an expected oxasilole derivative. It was converted to 3,4-diarylindole (151) by consecutive Suzuki–Miyaura and Hiyama cross-coupling reactions.

Scheme 35. Synthesis and Pd-catalyzed double cross-coupling reaction of 150.

4. Benzoxaborole Congeners and Related Ring-Expanded Systems Comprising B-O-Sn Linkage

There are only a few examples of heterocycles comprising B-O-Sn linkage fused with an aromatic core. The reaction of 1,8-bis(trimethylstannyl)naphthalene with BCl₃ afforded 1-(chlorodimethylstannyl)-8-(dichloroboryl)naphthalene (152). It underwent chloride–methyl exchange at elevated temperature to give compound 153, which was converted into the borinic acid derivative 1-(dichloromethylstannyl)-8-(hydroxymethylboryl)naphthalene (154). It was characterized by multinuclear NMR spectroscopy, and formation of a heterocyclic motif through dative B-O(H)→Sn interaction was confirmed by single crystal X-ray analysis (Scheme 36) [49].

Scheme 36. Synthesis of 154.

Recently, 1,1-dibutylnaphthoxastannaborinin-3-ol (155), featuring covalent B-O-Sn linkage was obtained in low yields by the heating of 8-iodonaphthalene-1-boronic acid with an excess of Bu₃SnOMe (Scheme 37) [50]. It was characterized in detail by single crystal X-ray diffraction analysis, which showed the formation of centrosymmetric H-bonded dimers.

Scheme 37. Synthesis of 1,1-dibutylnaphthooxastannaborinin-3-ol 155.

In addition, one can mention compound 156 with a ferrocene scaffold, where the formation of a heterocycle occurred through dative B-O(Me)→Sn interaction, resembling the situation observed in the naphthalene derivative (154). An extended complex (157) was isolated from the reaction of 156 with pseudoephedrine (Scheme 38) [51].

Scheme 38. Synthesis of ferrocene derivatives 156–157 with fused heterocycles formed through dative B-O(Me)→Sn bond.

5. Benzoxaborole Aza Analogues and Related Ring-Expanded Systems

Nitrogen benzoxaborole congeners comprising a five-membered heterocycle with B-O-N linkage have not been described in the scientific literature so far. However, replacement of the benzene aromatic ring with a pyridine one gave rise to pyridoxaboroles. Their synthesis started with 3-bromopyridine, which was converted to 6-butyl-2-(3′-bromo-4′-pyridyl)-(N-B)-1,3,6,2-dioxazaborocan (158), followed by Br/Li exchange and the trapping of a resulting lithiated intermediate with selected benzaldehydes to give pyridoxaboroles 159–161. Compound 161 was subjected to N-methylation, resulting in the cationic heterocycle (162). Pyridosiloxaborole (163) was obtained when Ph₂Si(H)Cl was used as an electrophilic reagent (Scheme 39) [52].

Scheme 39. Synthesis of pyridoxaboroles 159–162 and pyridosiloxaborole 163.

In a different approach, 2-fluoro-3-iodopyridine was subjected to LDA-induced deprotonation with concomitant halogen-dance isomerization, followed by the trapping of an aryllithium with 2-methoxybenzaldehyde. The resultant carbinol (164) was protected as a sodium salt, which was subjected to I/Li exchange with t-BuLi and subsequent boronation with B(OMe)₃ to give pyridoxaborole (165) (Scheme 40) [52]. In addition, pyridoxaboroles (166–168) were prepared recently and used in Suzuki–Miyaura cross-coupling reactions with selected halogenated N-methyl substituted pyrazinone and pyridazinone derivatives en route to novel Bruton’s tyrosine kinase (BTK) inhibitors, with the general structure shown in Scheme 41 [53].

Scheme 40. Synthesis of pyridoxaborole (165).

Scheme 41. Synthesis and Suzuki–Miyaura cross-coupling reactions of pyridoxaboroles 166–168.

Unlike structurally related benzoxaboroles, pyridoxaboroles are amphoteric compounds due to the presence of a basic nitrogen atom. ¹¹B NMR spectroscopy data point to formation of zwitterionic species featuring the protonated nitrogen atom and anionic boronate moiety in a mixed MeOH/D₂O solvent. The presence of the Lewis acidic boron and Lewis base N atom results in aggregation by means of N–B dative bonds, leading to the formation of a 1D coordination polymer of 161. However, the introduction of a 2-fluoro substituent at the pyridine ring weakens N–B coordination and therefore H-bonded chains involving BOH groups and pyridine N atoms are formed in the case of 165 [52]. Thus, pyridoxaboroles can serve as self-complementary tectons for generation of molecular networks through N–B coordination and/or hydrogen bonds, where the assembly can be changed by tuning the donor properties of the pyridine N atom. The specific behaviour of pyridoxaboroles results from their amphoteric character, higher boron Lewis acidity as compared to pyridineboronic acids (or esters), and the presence of two competitive electron deficient sites, i.e., the boron and the BOH hydrogen atoms.

Ring-expanded benzoxaborole aza analogues featuring the 6-membered boracycle with B-O-N=C linkage, termed oxazaborines or nitrono arylboronate esters, have been reported already in the 1950s [54,55,56,57,58,59,60,61]. The parent benzoxazaborine (169) was obtained by condensation of 2-formylbenzeneboronic acid with hydroxylamine (Scheme 42) [54,56]. Renewed interest in this heterocycle emerged in 1997 thanks to Groziak et al., who undertook comprehensive research on boron-nitrogen planar heterocycles displaying nucleic acid-like hydrogen bonding motifs [62]. The analogous benzoxazaborininone (171) was obtained by aminolysis of ester group in (2-(ethoxycarbonyl)phenyl)boronic acid with hydroxylamine, followed by intramolecular condensation of boronic and hydroxamic groups in the intermediate (170), leading to a target planar 6-membered boron heterocycle ring. The X-ray diffraction analysis showed the presence of lactam tautomer (171), rather than a lactim one (171′) (Scheme 43) [63].

Scheme 42. Synthesis of the parent benzoxazaborine 169.

Scheme 43. Synthesis of benzoxazaborininone 171.

Later, it was found that a simple three-component protocol involving the treatment of an appropriate chiral hydroxylamine with 2-formylphenylboronic acid and enantiopure BINOL leads to a mixture of diastereomeric nitrono-arylboronate esters, whose ratio can be determined by ¹H NMR analysis and reflects the optical purity of a starting hydroxylamine (Scheme 44a). As a secondary effect, these studies gave rise to a series 4-substituted zwitterionic benzoxazaborine complexes (172–179), obtained as mixtures of diastereomers (Scheme 44b,c) [64].

Scheme 44. General procedure for preparation of mixtures of distareomeric nitrono-borane esters 170–177 (a); Complexes formed in reaction with (R)-hydroxylamines (b) and (S)-hydroxylamines (c).

Recently, two functionalized benzoxazaborine derivatives (182–183) were synthesized via the S_N2 reactions of 7-hydroxybenzoxazaborines (180–181) and pleuromutilin tosylate (Scheme 45). It should be noted that the preparation of 180–181 was not reported. The pleuromutilin scaffold is a primary structural fragment of an important class of antibiotics. Thus, 182–183 were investigated as potential new anti-Wolbachia agents for the treatment of onchocerciasis and lymphatic filariasis [65]. Unlike benzoxaboroles, introduction of a fluorine atom did not improve antimicrobial potency, and only the EC₅₀ values obtained for 180 (14.2 nM for Wolbachia infected C6/36 cells and 5.1 nM for Wolbachia infected LDW1 cells) are promising.

Scheme 45. Synthesis of boracyclic pleuromutilin conjugates 182–183.

Another group of ring-expanded benzoxaborole aza analogues encompasses compounds with a 6-membered boracycle comprising B-O-C=N or B-O-C-N linkage, generally termed benzoxazaborines. They were reported for the first time over 60 years ago [66] but attracted increased interest only in the 1990s [67,68,69,70,71]. The parent benzoxazaborin (186) was synthesized by the reduction of (2-nitrophenyl)boronic acid (184) to (2-aminophenyl)boronic acid (185), which underwent condensation with acetic formic anhydride. 3-methyl and 3-trifluoromethyl substituted benzoxazaborines (187–188) were prepared analogously. Compound 187 was also synthesized from 184 via Parr hydrogenation in aqueous acetic acid, but this method was less efficient (Scheme 46) [68].

Scheme 46. Synthesis of 1,2,4-benzoxazaborines 186–188.

Zwitterionic benzoxazaborines featuring a four-coordinated boron atom (193–198) were also obtained. Thus, the treatment of 185 with selected alkyl isocyanates afforded respective diazaborine intermediates (189–191), which underwent condensation with pinacol to give 193–195. In addition, the reactions of compounds 189 and 190 with KHF₂ resulted in fluoro analogues 197 and 198. In the case of tert-butyl derivative (196), diazaborine pinacol ester did not form, but the problem was overcome by conversion of 185 to pinacol ester (192), followed by treatment with t-BuNCO (Scheme 47) [69,70]. In the methanolic solution, diazaborines 189, 199, and 200 also undergo reversible transformation to zwitterionic oxazaborine systems (201–203, respectively) (Scheme 48) [71].

Scheme 47. Synthesis of zwitterionic benzoxazaborines 193–198.

Scheme 48. Reversible formation of zwitterionic benzoxazaborines 201–203.

The potassium salt with oxazaborine anion (204) served as the intermediate in the synthesis, starting with o-bromotrifluoroacetanilide en route to functionalized triarylborane (205), which was expected to be an efficient fluoride receptor (Scheme 49) [72].

Scheme 49. Synthesis of 205 via ionic benzoxazaborine intermediate 204.

More extended benzoxazaborines comprising substituents, both in the boracyclic ring as well as in the aromatic core, were reported in 2009. The synthesis of 207 and 208 started from methyl 4-amino-3-bromobenzoate, which was converted to an appropriate phenylacetamido derivative followed by the Miyaura borylation. Subsequent deprotection of boronate ester (206) gave compound 207, which was additionally converted to benzoic acid derivative 208 (Scheme 50). Unfortunately, studies on the potential inhibitory activity of 207–208 against d,d-carboxypeptidase R39 did not give positive results [73]. In addition, an analogous variant of the deprotection reaction of pinacol boronate esters, utilizing milder NH₃ base instead of LiOH in the second step, was elaborated in order to obtain compounds 187, 207, and 209 (Scheme 51) [74].

Scheme 50. Synthesis of functionalized benzoxazaborines 207 and 208.

Scheme 51. Synthesis of oxazaborine derivatives 187, 207, and 209, utilizing the reaction of deprotection of o-amido pinacol phenylboronates via difluoroboranes.

Another functionalized derivative (210) was synthesized using 185 and 4-trifluoromethylphenyl isocyanate (Scheme 52). It was further subjected to investigation towards recognition of various guest molecules, especially warfare agents [75].

Scheme 52. Synthesis of compound 210.

Very recently, it was found that ortho-borylated N-phenyltetramethylguanidine (211) exhibits the Frustrated Lewis Pair (FLP) character, which enables formation of zwitterionic boracyclic adducts (212–215) through the insertion of carbonyl electrophiles such as H₂CO, PhCHO, and PhNCO (Scheme 53) [76].

Scheme 53. The use of the FLP effect for synthesis of boracycles 212–215 from ortho-borylated N-phenyltetramethylguanidine 211.

6. Benzophosphoxaboroles and Related Ring-Expanded Systems

Benzophosphoxaboroles can be generally defined as heterocyclic systems comprising P-O-B linkage. There are a few examples of such compounds, which can be regarded as phosphine oxide systems stabilized through intramolecular P=O→B coordination but are also depicted as zwitterionic structures with P⁺-O-B⁻ linkage. The synthesis of benzophosphoxaboroles 217 and 220, comprising cyclic peroxoboronate motifs, was achieved via ¹O₂ oxidation of ortho-(diphenylphosphino) phenyl boronates 216 and 219 and subsequent con-proportionation to ortho-boronated triphenylphosphine oxides (218 and 221) (Scheme 54) [77].

Scheme 54. Synthesis and transformation of benzophosphoxaboroles 217 and 220, comprising peroxoboronate motifs.

Directed ortho-metalation of bis(tert-butyl)phosphine oxide with t-BuLi, followed by boronation with B(OMe)₃ and reduction using LiAlH₄, afforded a water-stable benzophosphoxaborole (222) featuring a P=O-BH₂ moiety. It was converted to a mono-C₆F₅ derivative (223) through the nucleophilic attack of C₆F₅MgBr on the boron atom, followed by hydrolysis with a liberation of H₂ (Scheme 55) [78]. A analogous bis(C₆F₅)-substituted derivative (224) was obtained by treatment of lithiated bis(t-butyl)phosphine oxide with (C₆F₅)₂BH·SMe₂, followed by acidic quenching of an intermediate ate complex. Compounds 222–224 were characterized by X-ray diffraction, which confirmed the formation of typical single B-O bonds (bond lengths in the range of 1.550–1.584 Å). Crystallographic data were consistent with ¹¹B NMR chemical shifts, which confirmed the presence of the tetracoordinate boron atom. Furthermore, the ³¹P NMR resonances are deshielded by ca. 50 ppm compared to the starting phosphine oxide, which clearly reflects the strong O→B coordination.

Scheme 55. Synthesis of 222–224.

Another benzophosphoxaborole derivative (226) was obtained in a two-step protocol starting with O-borylation of Mes₂P(O)H, followed by thermally induced rearrangement of the intermediate phospinoxyborane (225) via intramolecular attack of the S_NAr nucleophilic P atom on the C-F bond, resulting in ring closure, with concomitant migration of fluoride to the boron atom (Scheme 56) [79].

Scheme 56. Synthesis of 226.

Ring-expanded benzophosphoxaborole congeners are based on peri-substituted naphthalene and acenaphthene frameworks. Thus, 1-(dimesitylboryl)-8-(diphenylphosphino)naphthalene was subjected to oxidation of the P(III) centre with I₂ followed by hydrolysis of ae P(V) hypercoordinated intermediate, producing phosphine oxide derivative 227, which showed strong P=O→B coordination according to X-ray diffraction analysis; it was in agreement with ¹¹B NMR chemical shift, pointing to the tetrahedral character of the boron atom. Additionally, ³¹P NMR resonance is significantly shifted to a lower field, which is characteristic for P=O systems coordinated to Lewis acid centres (Scheme 57) [80].

Scheme 57. Synthesis of 227.

Boroxine species 229, resulting from dehydrative cyclotricondensation of 5-diphenylphosphinoacenaphth-6-yl boronic acid (228) was susceptible to partial oxidation in moist air, involving only one of three phosphorus atoms to give compound 230 (Scheme 58) [81].

Scheme 58. Synthesis of 230.

A six-membered zwitterionic ring system (232), comprising an internal B-O bond separated from the phosphorus centre by a carbon atom was obtained by utilizing the distinctive FLP properties of an ambiphilic phosphinoborane i-Pr₂P(o-C₆H₄)BMes₂ 231 towards dipolar activation of phenyl isocyanate (Scheme 59) [82].

Scheme 59. Synthesis of zwitterionic compound 232.

Similar six-membered zwitterionic heterocycles (236–238) are also simply formed by the treatment of ambiphilic ortho-phosphinyl pinacolato and catecholato arylboranes (233–235) with paraformaldehyde. Interestingly, it was found that CO₂ can also be entrapped by 235 with the aid of CatBH as a reducing agent to give analogous system 239 (Scheme 60) [83].

Scheme 60. Synthesis of zwitterionic boron-phosphorus heterocycles 236–239.

The FLP behaviour of 234 was used for the trapping of in situ generated difluorocarbene to give a heterocyclic compound (240) featuring B-CF₂-P moiety. The ring expansion in 240 occurred upon heating with 4-chlorobenzaldehyde through insertion of a carbonyl group, resulting in compound 241 (Scheme 61) [84].

Scheme 61. Synthesis of ring-expanded compound 241.

Analogous 7-membered ring systems (242–244) were obtained by the ring opening of selected epoxides, mediated by the FLP compound 233 (Scheme 62) [85].

Scheme 62. Synthesis of ring-expanded compounds 242–244 from insertion of epoxides with FLP species 233.

7. Benzoiodoxaboroles

Benzoiodoxaborole heterocycles comprising trivalent iodine, oxygen, and boron were only reported in 2011 [86]. In addition to being benzoxaborole congeners, those systems are also structurally related to benziodoxoles, representing an important part of the group of hypervalent iodine compounds extensively exploited in organic synthesis as highly selective and environmentally friendly oxidizing agents [87]. A 1-Chlorobenzoiodoxaborole derivative (248) was synthesized in a simple two-step process involving chlorination of 2-fluoro-6-iodophenylboronic acid (246), followed by the hydrolysis of intermediate 247. Benzoiodoxaboroles (248–251), bearing acetoxy or trifluoroacetoxy substituent at the iodine atom were obtained by oxidation of iodophenylboronic acids (245–246) with bleach (~5% aqueous sodium hypochlorite) in acetic or trifluoroacetic acid. However, it was found that 1-trifluoroacetoxy derivatives 251 and 252 can be obtained in much higher yields (>90%) by the treatment of acetates 249 and 250 with an excess of CF₃CO₂H (Scheme 63) [86]. Hydrolysis of benzoiodoxaboroles 250 and 252, carried out under mild basic conditions, afforded 1-hydroxy-4-fluorobenziodoxaborole (253). Treatment of 250 with p-TsOH H₂O led to the formation of 1-tosyloxy-4-fluorobenzoiodoxaborole (254) (Scheme 64) [86].

Scheme 63. Synthesis of benzoiodoxaboroles 248–252.

Scheme 64. Preparation of benzoiodoxaboroles 253–254.

A slow (10 day) crystallization of 252 in methanol resulted in a unique tetrameric system (256) composed of four molecules of dimethoxy derivative 255, assembled through dative interactions between boron and endocyclic oxygen atoms. Thus, the aggregate features the central 8-membered B₄O₄ ring (Scheme 65) [86].

Scheme 65. Formation of tetrameric benzoiodoxaborole aggregate 256.

Crystallographic studies on benzoiodoxaboroles 248, 251, and 252, comprising the trigonal-planar sp² hybridized boron atom, indicates the presence of a planar five-membered iodoxaborole ring. The most noteworthy feature is the presence of unusually short endocyclic I–O bonds at 2.04–2.09 Å. In fact, they are the shortest ever observed for the five-membered iodine(III) heterocycles. Such a bond shortening, together with the heterocycle planarity, may point to some additional conjugation and possible aromatic character with the contribution of resonance structures shown in Scheme 66. However, DFT calculations of NICS(0) and NICS(1) indexes for 1-chloro- and 1-trifluoroacetoxy substituted benziodoxaboroles revealed low aromaticity of iodoxaborole heterocycle in comparison to typical aromatic rings [86].

Scheme 66. Resonance structures of a benzoiodoxaborole framework.

Compounds 249–252 were tested as oxidizing agents in reactions with various organic substrates. However, they exhibit lower activity than 1-hydroxy- and 1-acetoxybenzoiodoxoles and do not oxidize alcohols, even when combined with a catalyst such as BF₃ Et₂O [86].

More recently, a new generation of pseudocyclic ionic benzoiodoxaboroles bearing various aryl substituents at the iodine atom was developed [88]. These new hypervalent iodine compounds were synthesized from 1-acetoxybenzoiodoxaboroles 249 and 250 and arenes by treatment with trifluoromethanesulfonic acid under mild conditions. Five derivatives (257–261) with various substitution patterns on the aryl group attached to hypervalent iodine were successfully obtained (Scheme 67). X-Ray analysis of 259 and 260 confirmed a pseudocyclic benziodoxaborole structure with rather short intramolecular interactions between the iodine and oxygen (I-O distance in the range of 2.698–2.717 Å).

Scheme 67. Synthesis of pseudocyclic ionic 1-arylbenziodoxaboroles 257–261.

Compounds 258 and 261 serve as new efficient benzyne generators, triggered by water in room temperature [88]. They were tested in reactions with various model substrates. The resultant aryne adducts were obtained in moderate to good yields under mild conditions, with water as the only activator of the reaction (Scheme 68). This is particularly important considering the fact that most of the benzyne precursors known to date require harsh or strongly basic conditions for the efficient generation of the benzyne intermediate. Moreover, further research showed that the new 1-arylbenzoiodoxaboroles could also serve as chemoselective arylating reagents towards the aromatic ring of tert-butyl phenol (Scheme 69) [88].

Scheme 68. Aryne-trapping reactions involving pseudocyclic benzoiodoxaborole precursors 258 and 261.

Scheme 69. Arylation of 4-(tert-butyl)phenol with 258 and 261.

8. Conclusions

Heteroelement analogues of benzoxaboroles represent a diverse group of organoboron heterocycles. They exhibit strongly varying structural behaviour and different physicochemical properties. For example, benzosiloxaboroles can be regarded as close analogues of benzoxaboroles due to comparable stabilities of 5-membered oxaborole rings. In contrast, benzoxadiboroles are prone to hydrolytic ring opening. The Lewis acidity of the boron atom in presented systems also changes in a wide range, reflecting the strong effect of heteroatom substitution and other structural modifications with a special emphasis on fluorination of the aromatic ring. The varying properties open possibilities for many applications. Indeed, obtained systems have been used in organic synthesis as reagents or catalysts, fluorescence emitters for the construction of organic light-emitting diodes (OLEDs), and diol receptors, as well as potent antimicrobial agents. We hope that this review will stimulate further research in the area, which will result in the design of novel structures, including hitherto unknown heterocycles, e.g., comprising B-O-Ge or B-O-Sb linkage. Most importantly, the presented systems show significant practical potential, which should be exploited in future, especially for medicinal chemistry applications.