Heteroelement Analogues of Benzoxaborole and Related Ring Expanded Systems

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.


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.

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.
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 pKa of 3.0, which is among the lowest figures for boronic acids and related species. 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.
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 8oxyquinolinato 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)(16)(17)(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.
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 (λem = ca. 525 nm, Φ = 13-15%), resembling other organoboron 8-oxyquinolinato complexes. Interestingly, it is blue-shifted in solid state (λem = 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.
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)(22)(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]. Transformations of strong bidentate Lewis acids of a general formula o-C6F4(BR2)2, R = C 6 F 5 (19), and BR 2 = BC 12 F 8 (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(C 6 F 5 )2]2(µ-OR), R = Me, Ph, C 6 F 5 , and C6F4[BC 12 F 8 ]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)(22)(23) are effective co-catalysts of ethylene polymerization due to activation of dimethyl zirconocene (Cp 2 ZrMe 2 ), resulting in corresponding products with Cp 2 ZrMe + cation [15,18]. Compound 21 was also used for generation of stannylium cationic species 26 (Scheme 9) [19]. 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)(22)(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]. 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 stud- The analogous oxonium salt with (Et 2 O) 2 H + 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, H 2 O) (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/H 2 O 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]. 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]. 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 In addition, one can also mention herein the synthesis of a zwitterionic system (31) based on an anionic benzoxadiborole framework with a C 4 -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].  (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 arylaryl 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 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 arylaryl 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)(35)(36)(37) where hydroxyl groups were replaced with OMe, Cl, Me [23], or mesityl (Mes) substituents [24], respectively. Very recently, a structurally extended analogue of 32 based on bicyclohexene-perinaphthalene framework 38 was obtained using an analogous protocol involving brominelithium 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]. Very recently, a structurally extended analogue of 32 based on bicyclohexene-perinaphthalene framework 38 was obtained using an analogous protocol involving brominelithium 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]. 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 cata- 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 were reported as efficient catalysts of dehydrative amidation of carboxylic acids with amine substrates. Initially, they were employed for efficient preparation of various αand 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 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). One can also mention the unexpected synthesis of the fused polycyclic oxadiborepin (44) from the diboraanthracene precusor (43) which involved double arylation with 8bromo-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 1 H 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. One can also mention the unexpected synthesis of the fused polycyclic oxadiborepin (44) from the diboraanthracene precusor (43) which involved double arylation with 8bromo-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 1 H NMR studies on the structural behaviour of 44 revealed that it exists in equilibrium with the One can also mention the unexpected synthesis of the fused polycyclic oxadiborepin (44) from the diboraanthracene precusor (43) which involved double arylation with 8bromo-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 1 H 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.

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

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 Et 3 N 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. 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 17. Synthesis of benzosiloxaborole derivatives through intramolecular cleavage of B-C bond with SiOH group.
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]. 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 11 B 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]. 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 11 B 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].
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]. 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 11 B 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]. 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]. 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 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].
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]. It should be noted that formyl-substituted benzosiloxaboroles (87)(88)(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]. 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]. It should be noted that formyl-substituted benzosiloxaboroles (87)(88)(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]. It should be noted that formyl-substituted benzosiloxaboroles (87)(88)(89) are cleanly reduced to respective carbinol derivatives (91-93) using NaBH 4 , 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]. In addition, a formyl derivative (89) was successfully subjected to reductive amination with dopamine, giving rise to the benzosiloxaborole conjugate (103) (Scheme 28) [42]. In addition, a formyl derivative (89) was successfully subjected to reductive amination with dopamine, giving rise to the benzosiloxaborole conjugate (103) (Scheme 28) [42]. In addition, a formyl derivative (89) was successfully subjected to reductive amination with dopamine, giving rise to the benzosiloxaborole conjugate (103) (Scheme 28) [42]. 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)Me 2 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. 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. Structurally closely related 6-(chloropyridinyl-2-oxy)-7-fluorobenzosiloxaboroles (138-139) were also obtained using a standard protocol (Scheme 31) [45]. Structurally closely related 6-(chloropyridinyl-2-oxy)-7-fluorobenzosiloxaboroles (138-139) were also obtained using a standard protocol (Scheme 31) [45]. Structurally closely related 6-(chloropyridinyl-2-oxy)-7-fluorobenzosiloxaboroles (138-139) were also obtained using a standard protocol (Scheme 31) [45]. 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. 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 CDCl 3 solution. Remarkably, acetone-d 6 (141) undergoes rearrangement to form 8-membered heterocyclic borinic acid (142)  Structurally closely related 6-(chloropyridinyl-2-oxy)-7-fluorobenzosiloxaboroles (138-139) were also obtained using a standard protocol (Scheme 31) [45]. 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. 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 SiMe 2 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  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  were also subjected to studies on inhibition of β-lactamases KPC-and pAmpC-produced by Gram-negative rods. Those enzymes provide multiresistance 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].
The synthesis and use of ring-expanded analogues of benzosiloxaboroles is currently at the initial stage of development. 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 Ks 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. 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 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].

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

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)

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)

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-4pyridyl)-(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 Ph 2 Si(H)Cl was used as an electrophilic reagent (Scheme 39) [52].
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]. Unlike structurally related benzoxaboroles, pyridoxaboroles are amphoteric compounds due to the presence of a basic nitrogen atom. 11 B NMR spectroscopy data point to Unlike structurally related benzoxaboroles, pyridoxaboroles are amphoteric compounds due to the presence of a basic nitrogen atom. 11 B NMR spectroscopy data point to Unlike structurally related benzoxaboroles, pyridoxaboroles are amphoteric compounds due to the presence of a basic nitrogen atom. 11 B NMR spectroscopy data point to formation of zwitterionic species featuring the protonated nitrogen atom and anionic boronate moiety in a mixed MeOH/D 2 O 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 2fluoro 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. 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 1 H 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]. 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 1 H 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]. 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 1 H 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]. Recently, two functionalized benzoxazaborine derivatives (182-183) were synthesized via the SN2 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. Recently, two functionalized benzoxazaborine derivatives (182-183) were synthesized via the S N 2 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 EC 50 values obtained for 180 (14.2 nM for Wolbachia infected C6/36 cells and 5.1 nM for Wolbachia infected LDW1 cells) are promising.
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]. 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. 3methyl 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]. Zwitterionic benzoxazaborines featuring a four-coordinated boron atom (193)(194)(195)(196)(197)(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]. 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. 3methyl 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]. 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]. 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]. 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]. 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 NH 3 base instead of LiOH in the second step, was elaborated in order to obtain compounds 187, 207, and 209 (Scheme 51) [74]. 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]. 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].

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-Blinkage. The synthesis of benzophosphoxaboroles 217 and 220, comprising cyclic peroxoboronate motifs, was achieved via 1 O2 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]. 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].

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-Blinkage. The synthesis of benzophosphoxaboroles 217 and 220, comprising cyclic peroxoboronate motifs, was achieved via 1 O2 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]. 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]. 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].

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-Blinkage. The synthesis of benzophosphoxaboroles 217 and 220, comprising cyclic peroxoboronate motifs, was achieved via 1 O2 Scheme 52. Synthesis of compound 210.

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-Blinkage. The synthesis of benzophosphoxaboroles 217 and 220, comprising cyclic peroxoboronate motifs, was achieved via 1 O2 Scheme 53.
The use of the FLP effect for synthesis of boracycles 212-215 from ortho-borylated Nphenyltetramethylguanidine 211.

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 1 O 2 oxidation of ortho-(diphenylphosphino) phenyl boronates 216 and 219 and subsequent con-proportionation to ortho-boronated triphenylphosphine oxides (218 and 221) (Scheme 54) [77]. 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 11 B NMR chemical shifts, which confirmed the presence of the tetracoordinate boron atom. Furthermore, the 31 P NMR resonances are deshielded by ca. 50 ppm compared to the starting phosphine oxide, which clearly reflects the strong O→B coordination. Directed ortho-metalation of bis(tert-butyl)phosphine oxide with t-BuLi, followed by boronation with B(OMe) 3 and reduction using LiAlH 4 , afforded a water-stable benzophosphoxaborole (222) featuring a P=O-BH 2 moiety. It was converted to a mono-C 6 F 5 derivative (223) through the nucleophilic attack of C 6 F 5 MgBr on the boron atom, followed by hydrolysis with a liberation of H 2 (Scheme 55) [78]. A analogous bis(C 6 F 5 )-substituted derivative (224) was obtained by treatment of lithiated bis(t-butyl)phosphine oxide with (C 6 F 5 ) 2 BH·SMe 2 , 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 11 B NMR chemical shifts, which confirmed the presence of the tetracoordinate boron atom. Furthermore, the 31 P NMR resonances are deshielded by ca. 50 ppm compared to the starting phosphine oxide, which clearly reflects the strong O→B coordination. 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 11 B NMR chemical shifts, which confirmed the presence of the tetracoordinate boron atom. Furthermore, the 31 P NMR resonances are deshielded by ca. 50 ppm compared to the starting phosphine oxide, which clearly reflects the strong O→B coordination. 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 11 B NMR chemical shift, pointing to the tetrahedral character of the boron atom. Additionally, 31 P NMR resonance is significantly shifted to a lower field, which is characteristic for P=O systems coordinated to Lewis acid centres (Scheme 57) [80]. 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]. 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]. 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 I 2 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 11 B NMR chemical shift, pointing to the tetrahedral character of the boron atom. Additionally, 31 P NMR resonance is significantly shifted to a lower field, which is characteristic for P=O systems coordinated to Lewis acid centres (Scheme 57) [80]. 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 11 B NMR chemical shift, pointing to the tetrahedral character of the boron atom. Additionally, 31 P NMR resonance is significantly shifted to a lower field, which is characteristic for P=O systems coordinated to Lewis acid centres (Scheme 57) [80]. 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]. 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]. 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]. 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 11 B NMR chemical shift, pointing to the tetrahedral character of the boron atom. Additionally, 31 P NMR resonance is significantly shifted to a lower field, which is characteristic for P=O systems coordinated to Lewis acid centres (Scheme 57) [80]. 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]. 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]. 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]. 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 CO 2 can also be entrapped by 235 with the aid of CatBH as a reducing agent to give analogous system 239 (Scheme 60) [83]. 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]. 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]. 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].

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 CF 3

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].

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]. 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 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 B 4 O 4 ring (Scheme 65) [86].
Crystallographic studies on benzoiodoxaboroles 248, 251, and 252, comprising the trigonal-planar sp 2 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]. Crystallographic studies on benzoiodoxaboroles 248, 251, and 252, comprising the trigonal-planar sp 2 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]. 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). 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. Crystallographic studies on benzoiodoxaboroles 248, 251, and 252, comprising the trigonal-planar sp 2 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]. 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). 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. 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 BF 3 Et 2 O [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 65. Formation of tetrameric benzoiodoxaborole aggregate 256.
Crystallographic studies on benzoiodoxaboroles 248, 251, and 252, comprising the trigonal-planar sp 2 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]. 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). 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. 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].
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].

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 tions, 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].

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

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.