ライフサイエンスコーパス: boron

1 donation, despite the electron deficiency of boron.

2 ells allow the intracellular accumulation of boron.

3 lly at least, by formation of complexes with boron.

4 pecies 2 that possesses a planar tetraatomic boron(0) unit with the average oxidation state of zero.

5 the proton fusion reaction (P-BFT) and using boron-10 agent to capture the low energy secondary neutr

6 a radiation effectiveness enhancement, using boron-11 agent to initiate the proton fusion reaction (P

7 In addition, boron administration showed a marked reduction in myocar

8 ld acid/base treatment and maintain constant boron adsorption capacities for at least 10 regeneration

9 The boron adsorption rate constants of both frameworks, dete

10 Here, we show that boron-alkylated BODIPY photocages are capable of directl

11 In this review, we look at boron, an element that despite its nonmetal nature, low

12 of two constitutional isomers where only the boron and nitrogen positions change.

13 ate 2p elements-particularly carbon but also boron and nitrogen-to the heavier p-block elements such

14 boronophenylphosphonic acid-designed to have boron and phosphorus as an isoelectronic combination of

15 ions between the alkyl groups of the diol on boron and the chiral phosphoric acid catalyst influence

16 Borophene, a 2D allotrope of boron and the lightest elemental Dirac material, is the

17 ns progress through coordination between the boron and the phenolic oxygen.

18 Multiple bonds between boron and transition metals are known in many borylene (

19 nd smooth formation of a planar complex with boron and Zn(2+) ions concluded the presence of a TICT p

20 ich III extractable manganese, copper, zinc, boron, and iron in soils and (b) to assess accumulation

21 lation occurs at the carbon atom adjacent to boron, and room temperature hydroboration occurs across

22 that Ln can engage in covalent bonding with boron, and, in some members of the LnB(6) family, also e

23 nic communication between the closely spaced borons, and the attachment of electron-deficient pendent

24 Here, we report boron- and phosphorus-containing heterosiliconoids with

25 a phenomenon in BAs and a related material - boron antimonide, that has never been predicted or exper

26 The oxidation of alizarin red s (ARS) in the boron-ARS complex at MNP/CNT/GCE and the oxidation of ti

27 ceeding 1000 W m(-1) K(-1) in single-crystal boron arsenide (BAs) has led to interest in the potentia

28 s considerably lower for boron phosphide and boron arsenide as the identical isotopic mass disorder b

29 ons predict that the thermal conductivity of boron arsenide is second only to that of diamond, the be

30 , we identified Li(2)[4] (Me substituents at boron) as the best performing catalyst; its substrate sc

31 rinic acids reversibly bind catechol to form boron "ate" complexes (BACs) that alter the electron den

32 esult of the formation of a chlorine radical-boron 'ate' complex that selectively cleaves sterically

33 esters with alkyl lithium reagents provides boron-ate complexes.

34 y sensitive to the steric crowding about the boron atom, pointing to the crucial involvement of the G

35 able amount of spin density localized on the boron atoms (0.322 for 2 and 0.369 for 4).

36 d in BiB(2) O(-) [Bi=B-B=O](-) in which both boron atoms can be viewed as sp-hybridized and the [B-BO

37 anthracene framework and dislocation of the boron atoms from the planes of the phenyl rings they are

38 This mechanism was exploited to shuttle boron atoms into cancer cells for the application of bor

39 generating peptide conjugates with up to 80 boron atoms per molecule.

40 Branched conjugates loaded with up to 80 boron atoms per peptide molecule exhibited a maintained

41 ompared to heterocycles with two nitrogen or boron atoms, e.g., C(2)B(10)H(12) carboranes versus plan

42 y but at the same time sterically shield the boron atoms, resulting in a macrocycle that is both high

43 ral cages composed of alternating carbon and boron atoms.

44 eolite MCM-22 isomorphously substituted with boron (B-MWW).

45 icals (CH(3) (.) ) in the ODHP reaction over boron-based catalysts is achieved by using online synchr

46 -isolated BO(3) units are the active site in boron-based catalysts.

47 erstanding the ODHP reaction mechanisms over boron-based catalysts.

48 A sustainable boron-based catalytic approach for chemoselective N-alky

49 mical bonding, paving the foundation for new boron-based chemical compounds and nanomaterials.

50 powerfully demonstrated by the reactivity of boron-based molecules with H(2), CO, alkynes, alkenes an

51 Recent work has used boron-based proxies in planktic foraminifera to characte

52 Correction for 'Boron-based stimuli responsive materials' by Soren K.

53 en a boron cluster cage and an exopolyhedral boron-based substituent (e.g., -BF(3)K, -B(OH)(2)).

54 Reactions at the resulting carbon-boron bond show how these borylations can lead to the in

55 carbon and a synthetically versatile carbon-boron bond with control of stereoselectivity and regiose

56 o explore metastable synthesis of boron-rich boron-carbide materials.

57 s of stable crystal structures in boron-rich boron-carbide system and provides a pathway for large-ar

58 borinines display restricted rotation at the boron-carbon aryl bond, yielding conformational isomers

59 Here we demonstrate the formation of a boron-carbon bond between these substances in a two-step

60 performed to demonstrate the crucial role of boron catalyst for the activation of the intermediate di

61 lies unique features of highly electrophilic boron catalysts, such as tris(pentafluorophenyl)borane,

62 nctional indicators; and substitution at the boron center often renders the resultant BODIPY incompat

63 nced with increasing electrophilicity of the boron center.

64 with ionizable groups or substitution at the boron center.

65 The boron-centered radicals derived from alkenyl N-heterocyc

66 (+) featuring three bridge-bonds between two boron centers.

67 -carbons of the flanking Dipp groups and the boron centres of the diazaborolyl heterocycles, with K..

68 0.5 m H(2) SO(4) ) increases with increasing boron chain condensation in vanadium borides: Using a -2

69 tical V(x) B(y) phases containing at least a boron chain.

70 Herein, we report a new method, the boron-chalcogen mixture (BCM) method, for the synthesis

71 uranium chalcogenides based on the use of a boron-chalcogen mixture, where boron functions as an "ox

72 one of the most representative reactions in boron chemistry.

73 We report a carbon-boron clathrate with composition 2 La@B(6) C(6) (LaB(3)

74 Here, a new strategy utilizing a substituted boron cluster as a molecular dopant for conjugated polym

75 the direct oxidation of a B-B bond between a boron cluster cage and an exopolyhedral boron-based subs

76 is proposed to be delocalized throughout the boron cluster core.

77 ter unveiled the existence of fullerene-like boron clusters (borospherenes).

78 Here, we present polyhedral boron clusters (carboranes) as strongly binding, yet eas

79 onsequently, we conclude that aromaticity in boron clusters survives radical structural changes.

80 Metallacarboranes are a class of inorganic boron clusters that have recently been recognized as bio

81 carriers approximately matches the number of boron clusters, yielding a doping efficiency of ~100%.

82 The results suggest that boron coatings retain oxygen by forming oxidized boron s

83 calcium, iron, manganese, zinc, phosphorous, boron, cobalt, Vitamins A, D, B6, thiamine, riboflavin,

84 rs of diphenanthrioctaphyrin, as well as the boron complex formed from them, have been separated into

85 e reactivity of P2 toward a tetracoordinated boron complex has been explored as a potential tool for

86 s downstream functionalizations of the alkyl boron compounds.

87 ntial applications of the stimuli-responsive boron compounds.

88 tically versatile organo-boronate esters and boron containing bioactives.

89 borylation is utilised mainly for accessing boron containing conjugated organic materials, however r

90 tions to alkenyl boronates, and additions of boron-containing allyl moieties to N-H ketimines.

91 te was previously shown to be a bench-stable boron-containing building block for the synthesis of bor

92 olecules (QTAIM) calculations imply that the boron-containing fragment closely approaches a limiting

93 pleuromutilins modified by introduction of a boron-containing heterocycle on C(14) of the polycyclic

94 satile precursors for the synthesis of novel boron-containing heterocycles.

95 Boron-containing materials have recently been identified

96 Boron-containing materials, and in particular boron nitr

97 ization techniques that the surface of these boron-containing ODH catalysts oxidize and hydrolyze und

98 catalysed processes and requires halogen- or boron-containing substrates(3-6).

99 ttack on CO(2) combined with internal P=O to boron coordination.

100 s conjugate can be considered as a promising boron delivery agent for BNCT.

101 phase peptide synthesis to produce selective boron delivery agents for BNCT.

102 One of the reasons is the lack of selective boron delivery agents.

103 ny advantages, compared to the corresponding boron-derived reagents.

104 kenyl nitriles are obtained providing useful boron-dienenitrile building blocks that can be further f

105 n mind, a series of methine- and aza-bridged boron dipyrromethene (BODIPY) derivatives were synthesiz

106 f our approach, we quantitatively designed a boron dipyrromethene (BODIPY)-based AIEgen which exhibit

107 two heavier main group element analogues of boron-dipyrromethene (BODIPY) chromophores are described

108 gn pH-controllable singlet oxygen-generating boron-dipyrromethene (BODIPY) dyes.

109 These boron-dipyrromethene (BODIPY)-based molecular rotors are

110 Compound 8 significantly inhibited boron-dipyrromethene (BODIPY)-verapamil transport mediat

111 resolution) of single, fluorescently labeled boron-dipyrromethene-labeled ATP molecules in relaxed sk

112 tuted alkenes by enabling irreversible alpha-boron-directed insertion pathways to achieve otherwise c

113 The type of boron does not influence the dependencies of the indicat

114 the use of an sp(2)-bonded carbon microspot boron doped diamond (BDD) electrode for voltammetric mea

115 ochemical windows of polished and unpolished boron doped diamond (BDD) electrodes with hydrogen and o

116 m lattice of an industrial type interstitial boron doped palladium nanoparticle catalyst system (Pd-(

117 t progress and achievements in the growth of boron-doped (metal-like) and nitrogen and phosphorus-dop

118 des, boron-doped diamond electrode (BDD) and boron-doped carbon nanowalls (B:CNW) electrode, were use

119 We introduce a new boron-doped cyclophane, the hexabora[1(6) ]cyclophane B6

120 tigated mechanisms for biofouling control at boron-doped diamond (BDD) electrode surfaces polarized a

121 of magnitude lower than reported values for boron-doped diamond anodes.

122 Two different type of electrodes, boron-doped diamond electrode (BDD) and boron-doped carb

123 n saliva and sweat, using a surface-modified boron-doped diamond sensing interface (cross-validated w

124 Functions within these boron-doped molecules are derived from external stimuli

125 A heavily boron-doped silicon substrate silences the photovoltaic

126 aborate to the lithium carbonate electrolyte boron dopes the CNTs increasing their electrical conduct

127 Boron-doping has long been recognized as a promising LUM

128 n analysis revealed that the 4R/A mutant had boron efflux activity, suggesting that the ScBOR1p monom

129 les, while Suginome began the exploration of boron electrophiles.

130 Increasing the boron electrophilicity by the transformation of a borona

131 ding products obtained via aldol addition of boron enolates to enals using the same Evans oxazolidino

132 transition metal complexes as well as recent boron examples for the formation of nitrogen-element bon

133 ansition metal, A = A-group element, and B = boron) exhibit orthorhombic or tetragonal symmetry, with

134 In contrast, tetrad nests, created by boron extraction from B-SSZ-70 at various other location

135 Boron-free AI-2 is the preferred ligand for PctA and Tlp

136 poison (BP) candidate for long life soluble-boron-free core.

137 g from both the inclusion of only 1 equiv of boron from the diboron reagent and a requirement for nea

138 yzed coupling of an azide anion, we prepared boron-functionalized 9-amino-ortho-carborane that binds

139 the use of a boron-chalcogen mixture, where boron functions as an "oxygen sponge" to remove oxygen f

140 experimental evidence of the viability of 2D borons, giving rise to the concept of borophene.

141 of boron-modified derivatives or loss of the boron group with a subsequent oxidation of the phosphoru

142 erful method for introducing these and other boron groups into organic molecules because it can be us

143 Boron has been reported in recent years to augment the i

144 Importantly, boron has the potential to induce cardiomyocyte cell cyc

145 ructure, with carbon atoms inserted into the boron icosahedra and 2b sites in a alpha-tetragonal B(52

146 wo voltammetric methods for determination of boron in hazelnut, peanut, almond, raisin, prune and dat

147 hearts, highlighting a protective effect of boron in the ischemic heart.

148 Boron is a finite resource, which has been listed as a c

149 Although a requirement for boron is a well-established feature of vascular plants,

150 The alternative, here postulated, is that boron is, and always has been, potentially toxic, a feat

151 al record by combining a new high-resolution boron isotope-based CO(2) record with novel estimates of

152 eir unexpected dependence on temperature and boron isotope.

153 SEM imagery, skeletal trace elements and boron isotopes (delta(11)B) have been combined as a nove

154 (cBN) crystals with controlled abundance of boron isotopes and measured kappa greater than 1600 watt

155 wo research groups have suggested that using boron isotopes will lead to a radiation effectiveness en

156 Using boron loaded peptide conjugates, which address G protein

157 Due to its high boron loading and excellent GRPR selectivity, this conju

158 storage materials comprised of electron-poor boron materials combined with electron-rich nitrogen ele

159 synthesis of new conformationally restrained boron-methylated BODIPY photocages that absorb light str

160 Boron might be beneficial as a supplement in MI and may

161 A systematic study of radical boron migration in diboronate complexes to form syntheti

162 ions which also reveal the corresponding 1,3-boron migration in such diboronate complexes to be feasi

163 The 1,5-boron migration in the homologous series leading to 1,4-

164 It is shown that radical 1,2- and 1,4-boron migrations to provide geminal and 1,3-bisborylalka

165 e reaction, resulting in either formation of boron-modified derivatives or loss of the boron group wi

166 presence of an oxidant (I(2)) to afford the boron-modified phosphodiester analogues containing a P-B

167 Boron monofluoride (BF) is a diatomic molecule with 10 v

168 ction between surrounding N(2) molecules and boron nanodroplets incorporate into the tubular structur

169 e exposed BN edge surrounding the surface of boron nanodroplets which is constructed by the heterogen

170 Boron neutron capture therapy (BNCT) allows the selectiv

171 oms into cancer cells for the application of boron neutron capture therapy (BNCT), a noninvasive appr

172 Boron-neutron capture generates an energetic lithium nuc

173 The ABC-trilayer graphene/hexagonal boron nitride (ABC-TLG/hBN) moire superlattice provides

174 changes in cell stiffness and adhesion upon boron nitride (BN) and hydroxyapatite (HAP) nanoparticle

175 growth of single-crystal layers of hexagonal boron nitride (BN) and molybdenum disulfide (MoS(2)) cry

176 oclusters (~1.5 nm) deposited on defect-rich boron nitride (BN) nanosheet (Ni/BN) catalysts with high

177 One is the root growth mode, in which boron nitride (BN) species formed via the surface intera

178 raphene encapsulated between two crystals of boron nitride (BN), in which the rotational alignment of

179 We grew cubic boron nitride (cBN) crystals with controlled abundance o

180 cently, the van der Waals material hexagonal boron nitride (h-BN) has emerged as a robust host for qu

181 Although hexagonal boron nitride (h-BN) has recently been identified as a h

182 In this work, 2D monolayer hexagonal boron nitride (h-BN) is exploited as an ultrathin decora

183 Hexagonal boron nitride (h-BN) is regarded as a graphene analogue

184 Using hexagonal boron nitride (h-BN) to disperse the NPs doubles DNP enh

185 ing (NVRS) phenomenon in monolayer hexagonal boron nitride (h-BN), a typical 2D insulator, is reporte

186 ostructure comprising graphene and hexagonal boron nitride (h-BN), and show that ssDNA can be stretch

187 Monolayers of graphene and hexagonal boron nitride (hBN) are highly permeable to thermal prot

188 Hexagonal boron nitride (hBN) ceramics are expected to have wide a

189 2D hexagonal boron nitride (hBN) is a wide-bandgap van der Waals crys

190 uccessful effort to grow in situ a hexagonal boron nitride (hBN) nanocoating on a stainless-steel wir

191 phononic metasurface, a grating of hexagonal boron nitride (hBN) nanoribbons.

192 oparticles (Ag@AuNPs) incorporated hexagonal boron nitride (HBN) nanosheets and molecularly imprinted

193 insulating van der Waals layer of hexagonal boron nitride (hBN) provides an excellent interface diel

194 6) and thickness of the insulating hexagonal boron nitride (hBN)(7,8) used to encapsulate the graphen

195 map the local theta variations in hexagonal boron nitride (hBN)-encapsulated MATBG devices with rela

196 es from graphene encapsulated with hexagonal boron nitride and few-layer graphite.

197 limited to, conducting graphene, insulating boron nitride and semiconducting transition metal dichal

198 ct-free monolayers of graphene and hexagonal boron nitride are surprisingly permeable to thermal prot

199 at hyperbolic phonon polaritons in hexagonal boron nitride can overcome this fundamental trade-off.

200 s of phonon polaritons launched in hexagonal boron nitride capping layers via its interaction with th

201 t is observed in both graphite and hexagonal boron nitride channels but exhibits marked material-depe

202 bilayer graphene with the top and/or bottom boron nitride crystals), we observe prominent and robust

203 als and numerous defects, while 2D hexagonal boron nitride does not meet required dielectric specific

204 chanically exfoliated graphene and hexagonal boron nitride exhibit perfect Nernst selectivity such th

205 re we report three-nanometre-thick amorphous boron nitride films with ultralow kappa values of 1.78 a

206 ed polymers for soft matters and a hexagonal boron nitride flake for two-dimensional materials.

207 with resistivity values similar to those of boron nitride grown by chemical vapour deposition.

208 Our results demonstrate that amorphous boron nitride has excellent low-kappa dielectric charact

209 te isotropically over graphene and hexagonal boron nitride in the plane, leaving limited degrees of f

210 on polaritons in isotopically pure hexagonal boron nitride interacting with the surrounding dielectri

211 Hexagonal boron nitride is a large band-gap insulating material wh

212 er graphene sandwiched between two hexagonal boron nitride layers.

213 from structured polymer film, to polaritonic boron nitride materials, to isolated bacterial peptidogl

214 composed of interconnected hollow hexagonal boron nitride microtubes with nanoscopic wall-thickness,

215 d-bilayer graphene and ABC trilayer graphene/boron nitride moire superlattices(1-4).

216 electronic ordering in the bilayer graphene/boron nitride moire system.

217 noparticles like gold nanorods and hexagonal boron nitride nanosheets were also analyzed to demonstra

218 Boron nitride nanotubes (BNNT) uniformly dispersed in st

219 Despite boron nitride nanotubes (BNNTs) first being synthesized

220 Research interest in boron nitride nanotubes (BNNTs) has increased after the

221 The morphological analysis of the end of boron nitride nanotubes (BNNTs) using high-resolution tr

222 PT strands are adsorbed on hexagonal boron nitride near-parallel to the surface in islands wi

223 During the sintering process, cubic boron nitride particles incorporated into the hBN flake

224 oss-sectional imaging reveals that amorphous boron nitride prevents the diffusion of cobalt atoms int

225 c phonon polaritons propagating in hexagonal boron nitride ribbons is reported.

226 ATBG was intentionally broken by a hexagonal boron nitride substrate, with interactions having a seco

227 uperstructures in thin crystals of hexagonal boron nitride using atomic-force microscopy and nano-inf

228 on metal dichalcogenide(10,11) and hexagonal boron nitride(12) sandwich structures (also known as ato

229 oron-containing materials, and in particular boron nitride, have recently been identified as highly s

230 ructural analogies to hexagonal graphene and boron nitride, we demonstrate that such low dimensional

231 bilayers graphene encapsulated by hexagonal boron nitride.

232 ween channels made of graphene and hexagonal boron nitride.

233 wisted bilayer graphene aligned to hexagonal boron nitride.

234 transport measurements on graphene/hexagonal boron-nitride Hall bars and show that wider devices reve

235 Here we show that, in graphene-on-boron-nitride superlattices, Brown-Zak fermions can exhi

236 hosphorene and bismuthene), carbon nitrides, boron nitrides along with transition metal carbides and

237 Currently, the effect of boron on cardiac contractility and remodeling is unknown

238 s(dicarbollide)(1-) anion substituted at the boron or carbon sites by alkysulfamide group(s) as highl

239 The boron oxide can be separated from the reaction mixture t

240 ably small, with the planarity of the oxygen-boron-oxygen motif playing an important role in minimisi

241 trophiles, specifically silicon-, nitrogen-, boron-, oxygen-, and phosphorus-based electrophiles in t

242 The boron persulfide formally inserted phenyl acetylene into

243 ith additional sulfur gave the corresponding boron persulfide, a NHC-stabilized boradithiirane.

244 hancement of kappa is considerably lower for boron phosphide and boron arsenide as the identical isot

245 Collectively, the results show that boron positively impacted MI-induced HF and attenuated c

246 Crystalline and amorphous boron powders were used.

247 C(sp(3))-rich and sterically hindered alkyl boron reagents in a practical and modular manner.

248 e capricious coupling partners and 2-pyridyl boron reagents in particular are notorious for their ins

249 Furthermore, the reactivity of both boron reagents toward transmetalation is enhanced with i

250 technique to explore metastable synthesis of boron-rich boron-carbide materials.

251 calculations of stable crystal structures in boron-rich boron-carbide system and provides a pathway f

252 Little is known about life in the boron-rich hot springs of Trans-Himalayas.

253 inverse sandwich structures with monocyclic boron rings stabilized by two metal atoms.

254 This was enabled by exploitation of boron's ability to be chemically bound to compounds with

255 ders of magnitude higher than those of other boron-selective adsorbents.

256 The boron-selective PAFs demonstrate adsorption capacities t

257 up to 70% higher than those of a commercial boron-selective resin, Amberlite IRA743, and markedly fa

258 y beta-boryl radicals that undergo rapid 1,2-boron shift to form thermodynamically favored secondary

259 This is followed by 1,5-boron shift to give a rearranged boranorcaradiene.

260 how that doping the C-Dots with phosphate or boron significantly influences their excited-state dynam

261 lowering the interfacial energy between the boron silicate and zinc phase.

262 to the introduction of parts per millions of boron, sodium, and nitrogen.

263 al advantages of using arylboronic esters as boron sources in C-H borylation are discussed.

264 the characteristic isotopic distribution of boron specialized the presence of modified MAGs in MS an

265 R spectroscopy, we show that the majority of boron species in B-MWW exist as isolated BO(3) units, fu

266 shion through the relaxation of interstitial boron species, corresponding to a 50 degrees C modulatio

267 ra synthetic transformation into more stable boron species, such as pinacolboronic esters (Bpin), for

268 Reactions proceed via stereodefined boron-stabilized allylic Cu species formed by an enantio

269 and diastereoselective conjugate addition of boron-stabilized allylic nucleophiles to alpha,beta-unsa

270 esenting opportunities for a large family of boron-stabilized, carbon-based clathrates with ranging p

271 n coatings retain oxygen by forming oxidized boron states in the presence of deuterium plasmas and co

272 t to carbon substituents on the double bond, boron substituents accelerate the alkyne coupling.

273 ing a chiral intermediate with two different boron substituents and cobalt bound to the same carbon.

274 ic demands in the key activating role of the boron substituents, whereby sterically unencumbered boro

275 We designed a sulfur precursor employing a boron-sulfur bond, which enables controllable modulation

276 estigated, for the first time, the effect of boron supplementation on cardiac function, myocardial fi

277 (4)] by formal [2+2] cycloaddition to give a boron thiocarbonate-type product.

278 This shift occurs with stereoinversion at boron through a transition state with open-shell diradic

279 on followed by 1,2-aryl/alkyl migration from boron to carbon to give the alpha-arylated/alkylated alk

280 ry of borospherenes unveiled the capacity of boron to form fullerene-like cage structures.

281 o migration of the original CAAC ligand from boron to phosphorus and coordination of the added CAAC t

282 stereospecific 1,2-migration of groups from boron to sp(2) and sp(3) carbon centers.

283 This study provides the first example of a boron-to-metal charge-transfer complex and evidence of a

284 Lesser Antilles volcanic arc(3), we studied boron trace element and isotopic fingerprints of melt in

285 ive for the cell cycle marker Ki67 in the MI boron-treated rats compared to saline, indicative of inc

286 ent in systolic and diastolic functions with boron treatment compared to saline control.

287 mechanism of acetylene bromoboration in neat boron tribromide was studied carefully by means of exper

288 The method is based on the use of boron trichloride to activate the involved substitution

289 clic allenyl aryl ketones was examined using boron trifluoride etherate and indium triflate to mediat

290 , and aromatic aldehydes in the catalysis of boron trifluoride etherate.

291 An electron-precise metal-boron triple bond was first observed in BiB(2) O(-) [Bi=

292 the first electron-precise transition-metal-boron triple-bond species, we have produced IrB(2) O(-)

293 rt the first indirect observation and use of boron vertex-centered carboranyl radicals generated by t

294 er values for the samples in which amorphous boron was used.

295 duced in animals and borax, a sodium salt of boron, was administered for 7 days, p.o., 21 days post-i

296 nds, which enables phosphate coordination to boron with a concomitant, stereoretentive protonation of

297 metallic glasses (and others also containing boron) with a glass transition temperature of up to 1,16

298 covering a selection of applications of the boron-Wittig reaction to target compounds via subsequent

299 ons with carbonyl derivatives, the so-called boron-Wittig reaction, allows for the straightforward an

300 Complimentary to classical hydroboration and boron-Wittig reactions, a new, efficient access to cycli