ライフサイエンスコーパス: boronic acid

1 subtly changing the structure of the achiral boronic acid.

2 tected using the fluorescent probe, coumarin boronic acid.

3 MR study of the protodeboronation of an aryl boronic acid.

4 mponent in the coupling reaction, namely the boronic acid.

5 on-promoted transmetalation reaction of aryl boronic acid.

6 which undergoes cross-coupling with the aryl boronic acid.

7 sceptible to potent reversible inhibition by boronic acids.

8 s, as well as arylammonium salts directly to boronic acids.

9 ing reaction of diaryl diselenides with aryl boronic acids.

10 les the generation of a variety of protected boronic acids.

11 al groups such as alcohols, amines, and even boronic acids.

12 clotrimers, which are readily intercepted by boronic acids.

13 of trisubstituted-alkenyl alcohols with aryl boronic acids.

14 fonylhydrazones with aryl and heteroaromatic boronic acids.

15 anocatalytic strategy for the formylation of boronic acids.

16 dentifying bortezomib and additional peptide boronic acids.

17 ve coupling of methylene C-H bonds with aryl boronic acids.

18 y accessible from the commercially available boronic acids.

19 aryl phosphonium salts and coupled with aryl boronic acids.

20 lladium intermediate using 1.5 equiv of aryl boronic acid 2.

21 llowed by covalent coupling of 3-aminophenyl boronic acid (3-APBA).

22 rotocol provide details for preparation of a boronic acid (3-cyanopheylboronic acid) and a boronic es

23 alogue of the sensor that does not contain a boronic acid (4) responded nearly identically to 3 in th

24 Boronic acids act as Bronsted acid type receptors throug

25 shared the same functional groups (halides, boronic acids, alkenes, and alkynes, among other groups)

26 omplexation of particular diol groups by the boronic acid also enables selective transformations of m

27 etrahedral adducts with the B(III) center of boronic acids, although there is also evidence for some

28 as solved through the development of a novel boronic acid-amine copromoter system for glycosyl accept

29 ming Petasis reaction occurring between aryl boronic acids, amines, and glyoxylic acids to prepare al

30 We describe a boronic acid analogue possessing interesting and potent

31 Using a combination of boronic acid and 5-chlorosalicylic acid as the additives

32 alysis indicated the association behavior of boronic acid and AHB.

33 ep is a Suzuki-Miyaura coupling of a furan-3-boronic acid and an 8-halocoumarin, which is advantageou

34 red rate law includes a second order in both boronic acid and catechol moieties, and inverse second o

35 le an estimate of beta(11-1) for any pair of boronic acid and diol from their pKa values, is proposed

36 Boronic acid and esters have been extensively utilized f

37 on of the E-ring aryl chloride to a reactive boronic acid and its use in the synthesis of a systemati

38 ly dependent on the electronic nature of the boronic acid and more subtle electronic effects of the a

39 d antibody immobilization via interaction of boronic acid and oligosaccharide moiety found on Fc regi

40 via forming the cis-diol linkage between the boronic acid and sugar moieties.

41 Two additional processes compete when the boronic acid and the boronate are present in sufficient

42 the fluorination to take place ortho to the boronic acid and the other, toward an ipso substitution.

43 pi interaction between the substrate ligated boronic acid and the phosphate.

44 means of electro-polymerization of 3-Thienyl boronic acid and Thiophen.

45 a stereodynamic probe carrying complementary boronic acid and urea units achieves this goal with hydr

46 s allows greater reactivity with simple aryl boronic acids and allows coupling reactions to proceed t

47 Coupling of readily available boronic acids and diazo compounds has emerged recently a

48 H profiles gives shifted pKa values both for boronic acids and diol as a result of significant interd

49 bioorthogonal click reaction between abiotic boronic acids and diols.

50 e reaction was amenable to a variety of aryl boronic acids and disubstituted malononitriles, providin

51 Boronic acids and esters have critical roles in the area

52 The widespread use of alkyl boronic acids and esters is frequently hampered by the c

53 Many of the current applications of boronic acids and esters require materials with very low

54 ium catalyzed oxidative homocoupling of aryl boronic acids and esters to biphenyls has been recognize

55 thod of conversion of haloarenes directly to boronic acids and esters.

56 rylating carbocyclization of allenynes using boronic acids and focuses on the correlation between rea

57 rboxylates with vicinal donor aryl groups by boronic acids and potassium organotrifluoroborates under

58 ed 1,3-stereoselective conjugate addition of boronic acids and potassium trifluoroborates under metal

59 vast reagent space of commercially available boronic acids and proceeds at ambient temperature.

60 Enantioconvergent arylation reactions of boronic acids and racemic beta-stereogenic alpha-keto es

61 The cross-coupling of boronic acids and related derivatives with sp(2) electro

62 e stereochemistry of cross-couplings between boronic acids and Z-alkenyl halides.

63 mponent reaction involving terminal alkynes, boronic acids, and perfluoroalkyl iodides is presented h

64 reacting flow-generated diazo compounds with boronic acids, and their application in controlled itera

65 co-functionalizing AuNPs with 3-aminophenyl boronic acid (APB) and L-glutamic acid-(2,2,2)-trichloro

66 Fluorinated boronic acid-appended benzyl bipyridinium salts, derived

67 strategy, we present the use of fluorinated boronic acid-appended pyridinium salts in combination wi

68 The combination of a boronic acid-appended viologen and perylene diimide was

69 mponent probes were assembled with up to six boronic acid-appended viologens (BBVs): 4,4'-o-BBV, 3,3'

70 rs other than the Lewis acidity (pKa) of the boronic acid are at play.

71 Here pendant boronic acids are shown to enhance the cytosolic deliver

72 We show that pyridine boronic acids are unsuitable, but they can be halogen-mo

73 nd amines via (2-(thiophen-2-ylmethyl)phenyl)boronic acid as a highly active bench-stable catalyst.

74 e core have used organoboron dichlorides and boronic acids as the boron precursors.

75 The results can inform the use of boronic acids as they are increasingly utilized in the d

76 fluorination of allylic alcohols using aryl boronic acids as transient directing groups.

77 time, a general, electrophilic amination of boronic acids at ambient temperature.

78 assisted amidation of readily available aryl boronic acids at room-temperature under open-flask condi

79 tidine residues direct oxidative coupling of boronic acids at the backbone NH of a neighboring amino

80 study is reported where folic acid (FA) and boronic acid (BA) based cytosensors and their analytical

81 A multiligand set of boronic acid (BA) beta-lactamase inhibitors was obtained

82 Both are boronic acid based inhibitors, demonstrating that high s

83 able sensor is constructed of a fluorescent, boronic-acid based glucose indicating polymer coated ont

84 ts or through introduction of stoichiometric boronic acid-based additives.

85 ogression, we prepared a library of peptidyl boronic acid-based inhibitors.

86 Using a well-known boronic acid-based saccharide sensor (3), this work reve

87 eficient, electron-rich or ortho-substituted boronic acids better results are obtained with racemic a

88 1,3-syn diol motifs showed high affinity for boronic acid binding.

89 combination of glyco-gold nanoparticles and boronic acid biosensor system opens a way to study nonco

90 )F singlets was utilized to characterize the boronic acid/boronate equilibrium kinetics.

91 e boronic esters or the trimeric form of the boronic acids (boroxines) in solution.

92 ely couples not only heteroaryl halides with boronic acids but also heteroaryl halides with boronate

93 sors are often based on fluorophore-appended boronic acids, but these severely lack discriminatory po

94 arious substituted alkynyl/alkenyl boronates/boronic acids by this procedure to furnish a library of

95 Starting from benzo-[b]-thiophene-2-boronic acid (BZB), a nanomolar inhibitor of AmpC beta-l

96 Starting from benzo(b)thiophene-2-boronic acid (BZBTH2B), a nanomolar non-beta-lactam inhi

97 trabromopyrene and (4-(ethoxycarbonyl)phenyl)boronic acid can easily be coupled to prepare the requis

98 Pioneering work revealed that acyclic boronic acids can act as 'transition state analogue' inh

99 Here we show that boronic acids can be chemoselectively reacted in the pre

100 is that both electron-rich and electron-poor boronic acids can be coupled in high yields.

101 The efficacy of the new boronic acid catalyst was confirmed by its ability to ac

102 alkynyl bromide and pinacol ester of alkynyl boronic acid catalyzed by CuFe2O4 nanoparticles has been

103 H3Hg(+) ensued a fast transmetalation of TPE-boronic acid causing drastic reduction in the solubility

104 dy, we show that the profluorescent coumarin boronic acid (CBA) probe reacts with amino acid and prot

105 SX-517 is the first reported boronic acid chemokine antagonist and represents a novel

106 ng Pd-O-B linkages, a tri-coordinate (6-B-3) boronic acid complex and a tetra-coordinate (8-B-4) boro

107 high SERS enhancement to the glucose-alkyne boronic acid complex on substrate.

108 adium-oxygen-boron linkages, a tricoordinate boronic acid complex, and two tetracoordinate boronate c

109 alized boronic acid to form a glucose-alkyne-boronic acid complex.

110 d (PBA) binds to both ARS and HbA1c via diol-boronic acid complexation.

111 The resulting PtNHase-boronic acid complexes represent a "snapshot" of reactio

112 tants (Kd) of the biotin-avidin and dopamine-boronic acid complexes were determined to be 15 +/- 1 fM

113 eboronation of polyfluoroaryl and heteroaryl boronic acids complicates their use in Suzuki-Miyaura co

114 bility using isobutylboronic acid as a model boronic acid compound.

115 A triosmium carbonyl cluster-boronic acid conjugate is used as a secondary carbohydra

116 ns using a homologous series of seven phenyl boronic acids conjugated to a polyethylene glycol, eight

117 In reactions with aryl boronic acids containing EWG at the para position, there

118 ide was developed through incorporation of a boronic acid-containing cleavable linker between polycat

119 al engineering, where double-H-bonding donor boronic acids could act as suitable organocatalysts or t

120 acilitated by Lewis acid assistance from the boronic acid coupling partner and an ionic S(N)1-like me

121 ronic acid (SX-517), a potent noncompetitive boronic acid CXCR1/2 antagonist.

122 t can be converted to trifluoroborate salts, boronic acids, cyclopropylarenes, cyclopropylamines, and

123 ploys an air-stable diethanolamine-complexed boronic acid (DABO boronate) as the allyl transfer reage

124 f a new type of hybrid biomaterial, namely a boronic acid-decorated lectin (BAD-lectin), for efficien

125 eworks with compositions ranging from highly boronic acid-deficient to networks with catechol voids.

126 r molecule based on a 2-hydroxymethyl phenyl boronic acid derivative binds even at neutral pH to the

127 to electrophilic amination of several common boronic acid derivatives (e.g., pinacol esters).

128 A variety of aryl boronic acid derivatives and dialkylmalononitriles were

129 The reaction tolerates various boronic acid derivatives and functional groups.

130 Functionalized O-heterocyclic boronic acid derivatives are produced using this transfo

131 t synthesis of pyridine-based heteroaromatic boronic acid derivatives is reported through a novel dib

132 sing achiral or racemic acyclic alkenols and boronic acid derivatives is reported.

133 porphyrin and its Suzuki cross coupling with boronic acid derivatives.

134 reported efflux pump inhibitory activity of boronic acid derivatives.

135 ul and pharmaceutically relevant alpha-amino boronic acid derivatives.

136 e variation of the dye structure through the boronic acid derived moiety (approach (b)) enables the f

137 A series of boronic acid derived salicylidenehydrazone (BASHY) compl

138 Stability constants of boronic acid diol esters in aqueous solution have been d

139 acter spp were evaluated using the cefotetan-boronic acid disk test and the cefotetan-cloxacillin Ete

140 thereby facilitating synthesis of the alkyl boronic acid drugs Velcade and Ninlaro as well as a boro

141 ient where one molecule was attracted to the boronic acid end of the gradient, and the other to the c

142 Rapid and direct: the carboxylation of boronic acid esters with (11)CO(2) provides [(11)C]carbo

143 MIDA boronates (N-methylimidodiacetic boronic acid esters) serve as an increasingly general pl

144 he alkyne group of the alkyne-functionalized boronic acid exhibits a distinct Raman peak at 1996 cm(-

145 While 2- and 4-substituted aryl boronic acids favored the (R)-enantiomer with most of th

146 action scope, including the use of different boronic acids, five-, six-, and seven-membered cyclic en

147 The use of bis-boronic acid for the direct synthesis of boronic acids h

148 Large collections of chemically diverse boronic acid fragments are commercially available becaus

149 olution greatly enhanced the emission of the boronic acid functionalized dye by a factor of up to 18.

150 olume resetting agent is incorporated into a boronic acid functionalized hydrogel containing an embed

151 trochemical cytosensor was designed based on boronic acid-functionalized polythiophene.

152 1-naphthaleneboronic acid and acenaphthene-5-boronic acid gave corresponding o-naphthyl benzaldehydes

153 developed and optimized with N-Boc-indole-2-boronic acid giving access to alpha-indole-gamma-substit

154 functional groups, and should allow for the boronic acid group to be used as an effective traceless

155 nd reversible binding of the analyte via the boronic acid group, amplification of SERS signals by the

156 The use of a monomer bearing a boronic acid group, with its ability to specifically int

157 dation of BDBA resulted in the conversion of boronic acid groups to phenol groups.

158 ylation of gamma-vinyl-gamma-lactone by aryl boronic acid has been developed.

159 alkyl primary amines from the corresponding boronic acids has been achieved at ambient temperature m

160 ng reactivity of Au(III)-F species with aryl boronic acids has been studied in detail taking advantag

161 bis-boronic acid for the direct synthesis of boronic acids has greatly facilitated the two-step, one-

162 Boronic acids have been shown to be potent inhibitors of

163 of the current methods for the synthesis of boronic acids, however, require transition metal catalys

164 roteins in complex samples using fluorescent boronic acids in gel electrophoresis.

165 sociation constant (Ka) of ortho-substituted boronic acids in solution showed that Ka for 1:1 associa

166 tuted-3-iodoquinolin-4(1H)-ones with several boronic acids in water using Pd(OAc)2 as a catalyst and

167 ng-opening reaction of vinylcyclopropanes by boronic acids in water, using palladium nanoparticles fo

168 (alpha-Amidoalkyl)boronic acids include biochemically significant serine p

169 A panel of boronic acid inhibitors was designed and tested against

170 conversion of aryl, heteroaryl, and alkenyl boronic acids into sulfinate intermediates, and onwards

171 ve rapid and high-yielding conversion of the boronic acids into the corresponding sulfinates.

172 idate that the ipso amination of substituted boronic acids involves the formation of cyanamidyl/arylc

173 -coupling between alkyl-carboxylic acids and boronic acids is described.

174 coupling of 1-aryl-2,2-difluoroalkenes with boronic acids is described.

175 t of a gold(I)-catalyzed sulfination of aryl boronic acids is described.

176 ditions from both organotrifluoroborates and boronic acids is described.

177 f heteroatom nucleophiles, O-alkylation with boronic acids is rare.

178 nes and barbituric acids, respectively, with boronic acids is reported.

179 its nitrile-N center with boron atom of the boronic acids, leading to chemoselective primary aminati

180 for aqueous-organic protodeboronation of 18 boronic acids, many widely viewed as unstable, have been

181 We have developed a synthetic boronic acid mask that restrains the ribonucleolytic act

182 ol chemiluminescence (CL) biosensor based on boronic acid modified gold substrate has been developed

183 Detection with a SSM boronic acid-modified SiNW-FET of the dopamine released

184 The boronic acid moiety confined within the lamellar morphol

185 The boronic acid moiety greatly accelerates the initial form

186 nsor, pnGFP, based on the incorporation of a boronic acid moiety into a circularly permuted green flu

187 is achieved by introduction of a C-terminal boronic acid moiety into dipeptidic inhibitors of the Zi

188 A boronic acid moiety was found to be a critical pharmacop

189 A boronic acid moiety was site-specifically introduced int

190 h conditions amenable to the presence of the boronic acid moiety which was considered important for t

191 exahydroxytriphenylene and 1,4-phenylene bis(boronic acid) monomers in solution.

192 preparation of reactive allylic and benzylic boronic acids, obtained by reacting flow-generated diazo

193 ween alpha-hydroxycarboxylate of citrate and boronic acids of BDBA.

194 llowed expedient preparations of alpha-amino boronic acids, often with high stereoselectivity, thereb

195 show that the suppressive effect of peptide boronic acids on hyperactive Wnt signaling is dependent

196 the aid of boronate probes, e.g. coumarin-7-boronic acid or 4-boronobenzyl derivative of fluorescein

197 ent, the imino group that forms ortho to the boronic acid or boronate ester group can form a dative N

198 romodibenzo[15]crown-5 and the corresponding boronic acids or borolanes via Suzuki cross-coupling and

199 N-tosylhydrazones, dihalogenated arenes, and boronic acids or boronate esters was developed, producin

200 d in trimeric forms (RBO3) commonly known as boronic acids or boroxins; obtaining their monomers has

201 with a range of aryl, heteroaryl, and styryl boronic acids or esters has been developed.

202 s-coupling of a triflate 6 with (hetero)aryl boronic acids or esters.

203 lyst to generate carbon radicals from either boronic acids or esters.

204 Aryl boronic acids or pinacol esters containing EDG were conv

205 yl-Bpin, p-tolyl-Bcat) and the corresponding boronic acid (p-tolyl-B(OH)2) in this type of cross-coup

206 A wide range of sensitive boronic acids, particularly polyfluoroaryl substrates th

207 erine beta-lactamase inhibitors containing a boronic acid pharmacophore, with the goal of finding a p

208 However, aryl boronic acid pinacol (BPin) ester reagents can be diffic

209 presence of ostensibly equivalently reactive boronic acid pinacol (BPin) esters by kinetic discrimina

210 reactions from (S)-nicotine containing a C-4 boronic acid pinacol ester group.

211 ) = 6-morpholino-2,2':6',2''-terpyridine-6''-boronic acid pinacol ester) to promote directed Lewis ac

212 inophenol and a Z- or an E-gamma-substituted boronic acid pinacol ester.

213 the formal homologation of aryl and alkenyl boronic acid pinacol esters.

214 d isocoumarins and 2-pyrones are isolated as boronic acids, pinacolboronate esters, or potassium orga

215 efficiency of arylboron-based nucleophiles, boronic acid, potassium trifluoroborate, neopentylglycol

216 traceless protection of the C3/C5 diol with boronic acids prior to glycosylation.

217 d Luciferin-2 (PCL-2), a H(2)O(2)-responsive boronic acid probe that releases 6-hydroxy-2-cyanobenzot

218 n peroxide using hydropropidine and coumarin boronic acid probes, respectively.

219 tructure-activity analyses using a series of boronic acid proteasome inhibitors and correlate cytotox

220 ent coupling of Selectfluor, a styrene and a boronic acid, provides chiral monofluorinated compounds

221 Condensation of oximes with boronic acids RB(OH)2 or B(OH)3 affords remarkably stabl

222 Boronic acids readily form boronate esters with the 1,2-

223 ted using a SNAP-tag approach to install the boronic acid reagent onto the extracellular domain of th

224 We repurposed the approximately 650 boronic acid reagents in our collection as a directed fr

225 An array of three water-soluble boronic acid receptors in combination with (19)F NMR spe

226 eptor pair and (b) functional tuning via the boronic acid residue.

227 Non-ortho-substituted boronic acids result in "flat" complexes.

228 died catalysts, meta-alkoxy substituted aryl boronic acids resulted in the (S)-enantiomer when used i

229 e nature of the adduct and the effect of the boronic acid's pK(a)(B) on the stability constant of the

230 rodeposited screen-printed electrode through boronic acid-saccharide interactions, with the boronic a

231 A ferrocenium boronic acid salt activates allylic alcohols to generate

232 rol experiments in the presence of competing boronic acids showed no crossover side-products and conf

233 Control of boronic acid solution speciation is presented as a new s

234 Control of boronic acid speciation is presented as a strategy to ac

235 e including the final trapping of a reactive boronic acid species with an aldehyde to generate a rang

236 ic, squarylium cyanine dye functionalized by boronic acid ("SQ-BA") was designed and synthesized for

237 een SWNT photoluminescence quantum yield and boronic acid structure.

238 a data set in which both the phosphoric and boronic acid structures were systematically varied, key

239 H-bond paired the adenine moiety of ATP, the boronic acid substituent of thiophene 3 covalently bound

240 to an aryl ketone or aldehyde with an ortho-boronic acid substituent.

241 ween vicinal hydroxyl groups of arabitol and boronic acid substituents of the bithiophene functional

242 ithiophene) derivatives bearing cytosine and boronic acid substituents, in the presence of the inosin

243 Boronic acid-substituted shapeshifting bullvalenes beari

244 Herein, we report on boronic acid-substituted stilbenes that limit TTR amyloi

245 With EWG meta to the boronic acid, substitution ipso to the boron moiety take

246 ctions of benzylic alcohols, including other boronic acids such as 2,3,4,5-tetrafluorophenylboronic a

247 popular C-C bond forming reactions of these boronic acids, such as the Suzuki-Miyaura, Heck, and Hay

248 ons (hydrophobicity, aromaticity, branching, boronic acids) suggest that the best siCPDs act differen

249 BL detection by the CLSI disk test (CLSI), a boronic acid-supplemented CLSI disk test (CLSI plus BA),

250 Boronic acid-supplemented tests can enhance ESBL detecti

251 ity exceeding 95%, with the exception of the boronic acid synergy test (88%) and modified Hodge test

252 ohort, sensitivities ranged from 72% for the boronic acid synergy test for the detection of KPC produ

253 arba assay, the Modified Carba NP assay, the boronic acid synergy test, and the metallo-beta-lactamas

254 ow protodeboronation, as do 3- and 4-pyridyl boronic acids (t0.5 > 1 week, pH 12, 70 degrees C).

255 Such an approach employed thiophene-3-boronic acid (T3BA) as paratope orientation controller,

256 elf-assembled monolayer (SAM) of thiophene-3-boronic acid (T3BA) is provided to modify the gold elect

257 DD.AA-type complexes of a series of aromatic boronic acids that adopt a syn-syn conformation with sui

258 By applying the process to other boronic acids, the synthesis of structurally diversified

259 enantioselective organocatalysed transfer of boronic acid to 5-hydroxyfuran-2(5H)-one, followed by an

260 s and (ii) sequential disproportionations of boronic acid to borinic acid and borane.

261 ondary binding with an alkyne-functionalized boronic acid to form a glucose-alkyne-boronic acid compl

262 Csp2 coupling of alkynyl bromide and alkenyl boronic acid to provide conjugated 1,3-enynes.

263 tal-free coupling of a tosyl hydrazone and a boronic acid to the preparation of a complex natural pro

264 epared through Rh-catalyzed addition of aryl boronic acids to 2,2-disubstituted malononitriles.

265 action tolerates a variety of functionalized boronic acids to afford a cis-fused bicyclic framework c

266 ing of benzylic ammonium triflates with aryl boronic acids to afford diarylmethanes and diarylethanes

267 o-enol esters were subsequently coupled with boronic acids to afford tetrasubstituted alkene derivati

268 )-catalyzed enantioselective 1,4-addition of boronic acids to electron-deficient alkenes is reported.

269 the peculiar dynamic covalent reactivity of boronic acids to form tetraboronate derivatives, interes

270 lysed Csp(3) Suzuki coupling of acetals with boronic acids to generate benzylic ethers, a reaction th

271 unanimously in the related addition of aryl boronic acids to methacrylate derivatives.

272 ge of alkyl boronic esters and aryl or alkyl boronic acids to react with electron-deficient olefins v

273 OF-5 structure can form over a wide range of boronic acid-to-catechol ratios, thus producing framewor

274 arged dye molecules was demonstrated using a boronic acid-to-cationic gradient where one molecule was

275 ium-catalyzed carbonylative coupling of aryl boronic acids together with terminal alkynes and perfluo

276 Boronic acid transition-state analogues are able to reve

277 Boronic acid transition-state inhibitors (BATSIs) repres

278 In contrast, 2-pyridyl and 5-thiazolyl boronic acids undergo rapid protodeboronation (t0.5 appr

279 Cyclopropyl and vinyl boronic acids undergo very slow protodeboronation, as do

280 ronic acid-saccharide interactions, with the boronic acid units specifically binding to the glycosyla

281 timal conditions for the slow release of the boronic acid using KOH as the base in biphasic THF/water

282 ere included in the investigations with each boronic acid varying in the substituent at its 4-positio

283 acid drugs Velcade and Ninlaro as well as a boronic acid version of the iconic antibiotic vancomycin

284 donocardia thermophila JCM 3095 (PtNHase) by boronic acids via kinetics and X-ray crystallography.

285 ion of aldehydes has been accomplished using boronic acids via the synergistic combination of copper

286 for the interconversion of diverse protected boronic acids, via intermediate organotrifluoroborates.

287 th cytosine and bithiophene derivatized with boronic acid were used as functional monomers.

288 and p-halophenols with o-, m-, and p-phenol boronic acids were investigated for all combinations und

289 o preserve the often sensitive C-B bond, all boronic acids were readily converted to their more stabl

290 irect benzylation between tosylhydrazone and boronic acid, which allowed the generation of structural

291 on transition state analog, benzothiophene-2-boronic acid, which was also isotopically enriched with

292 ling reactions involving aryl sulfamates and boronic acids, which operates at a significantly lower c

293 hydrolysis, resulting in fast release of the boronic acid while reagents bearing, for example, alkyny

294 rocess involves etherification of an alkenyl boronic acid with N-hydroxyphthalimide followed by a [3,

295 site-selective, copper-promoted couplings of boronic acids with carbohydrate derivatives.

296 described transnitrilative cyanation of aryl boronic acids with dialkylmalononitriles, the present re

297 This reaction is amenable to a wide range of boronic acids with different biorelevant functional grou

298 An efficient transnitrilation of aryl boronic acids with dimethylmalononitrile (DMMN) is descr

299 The photocatalytic hydroxylation of boronic acids with methylene blue as photosensitizer pro

300 endent, and varied substantially between the boronic acids, with rate maxima that varied over 6 order