ライフサイエンスコーパス: carboxylic

1 r (1R,3S,4S)-3-amino-4-fluoro cyclopentane-1-carboxylic acid (1), in this work, we rationally designe

2 inhibitor, 1,4-dihydrophenonthrolin-4-one-3-carboxylic acid (1,4-DPCA/hydrogel), to promote regenera

3 oxyphenyl]-8,9-dihydro-7H-benzo[7]annulene-2-carboxylic acid (43d), showing promising antitumor activ

4 cluding pyocyanin (PYO), 5-methylphenazine-1-carboxylic acid (5-MCA), and 1-hydroxyphenazine (OHPHZ),

5 rfluorononanoic acid), and 6:2 fluorotelomer carboxylic acid (6:2 FTCA).

6 hree US samples, where the 7:3 fluorotelomer carboxylic acid (7:3 FTCA) was prevalent.

7 mino-3-fluoro-4-(fluoro-(18)F)cyclopentane-1-carboxylic acid ([(18)F]28) have been prepared in 10 and

8 mino-3-fluoro-4-(fluoro-(18)F)cyclopentane-1-carboxylic acid ([(18)F]9) and (1S,3S,4R)-1-amino-3-fluo

9 he beta-lactam antibiotic, 1-carbapen-2-em-3-carboxylic acid (a carbapenem).

10 iated stabilization of 1-aminocyclopropane-1-carboxylic acid (ACC) synthases (ACSs), the rate-limitin

11 the ethylene precursor 1-aminocyclopropane-1-carboxylic acid (ACC) was found to promote the emergence

12 s immediate precursor, 1-aminocyclopropane-1-carboxylic acid (ACC), is a non-proteinogenic amino acid

13 ng 3a-hydroxyhexahydropyrrolo[2,3-b]indole-2-carboxylic acid (HPIC) in a single, scalable step with e

14 ,5-tetrahydro-5-oxo-imidazo[1,2-a]pyridine-7-carboxylic acid (IPCA).

15 hydration of Hyp to (S)-Delta(1)-pyrroline-5-carboxylic acid (P5C).

16 e metabolites including Delta1-piperideine-6-carboxylic acid (P6C), alpha-aminoadipic semialdehyde (a

17 e synthesized a water-based ink using pyrene carboxylic acid (PCA) through non-covalent pai-pai stack

18 oss; low urocanic acid (UCA) and pyrrolidone carboxylic acid (PCA), both of which are filaggrin break

19 degradation of emerging perfluoroalkyl ether carboxylic acid (PFECA) pollutants with ultraviolet-gene

20 Protonation to form phosphine carboxylic acid (PH(2) COOH) and functionalization to fo

21 -N formation that proceeds through a cascade carboxylic acid activation, acyl azide formation, Curtiu

22 cts with CO(2) to generate the corresponding carboxylic acid after protonation.

23 Several 3,4-dihydroxycyclohexane carboxylic acid analogues can be employed for chain rele

24 ,4S)-3-amino-4-(3-boronopropyl)pyrrolidine-3-carboxylic acid analogues with up to a 1000-fold increas

25 d for the conductance of TPA bridged through carboxylic acid anchoring groups (3.8 x 10(-4)-3.2 x 10(

26 esign due to not only their bioisosterism to carboxylic acid and amide moieties but also to their met

27 A Ugi four-component reaction with indole-2-carboxylic acid and an aniline followed by a Pd-catalyze

28 size a series of enantiopure, pinene-derived carboxylic acid and dimer ester homologues.

29 hed beta-thio-alpha-hydroxy and alpha-chloro carboxylic acid and ester building blocks by diazotizati

30 not impair its ability to act as an ordinary carboxylic acid and to efficiently protonate physiologic

31 king isatoic anhydride-8-amide from isatin-7-carboxylic acid as a tool to easily produce a range of q

32 tified a methyl substitution adjacent to the carboxylic acid as an appropriate means to accomplish fa

33 ent obtained from the oxidation of ferrocene carboxylic acid as the electrochemical probe.

34 Starting from simple carboxylic acid building blocks, this modular sequence e

35 We report that a readily accessible chiral carboxylic acid catalyst exerts control over asymmetric

36 The flexibility of the hydroxyl carboxylic acid catalyst leads to significant difference

37 The high acidity of the carboxylic acid catalyst, which exceeds that of the well

38 ism of the asymmetric BINOL-derived hydroxyl carboxylic acid catalyzed allylboration of benzaldehyde

39 The construction of carboxylic acid compounds in a selective fashion from lo

40 cage is capable of co-encapsulating multiple carboxylic acid containing guests in its cavity, and the

41 utility of the E-RANSY method by extracting carboxylic acid containing metabolites from human urine,

42 lites generated from energy expenditure, tri-carboxylic acid cycle, tocopherol, polyamine metabolism,

43 such, the invention of new reactions between carboxylic acid derivatives and amines that strategicall

44 ubstituted piperidines with aryl, alkyl, and carboxylic acid derivatives at multiple different sites.

45 sformations that allow for the conversion of carboxylic acid derivatives to functional groups bearing

46 The reaction of carboxylic acid derivatives with amines to form amide bo

47 Carboxylic acid derivatization produces a broad range of

48 ide esters (primary, secondary, and tertiary carboxylic acid derived), several saturated and unsatura

49 ts in the synthetic sequence relative to the carboxylic acid ester.

50 the intermolecular radical C-H amination of carboxylic acid esters with organic azides via Co(II)-ba

51 ketone synthesis that couples two different carboxylic acid esters, N-hydroxyphthalimide esters and

52 oved applicable to a variety of (hetero)aryl carboxylic acid fluorides as well as diverse diboron rea

53 N-alkyl pyridinium salts with in situ formed carboxylic acid fluorides or 2-pyridyl esters under redu

54 nickel-catalyzed decarbonylative coupling of carboxylic acid fluorides with diboron reagents to selec

55 scent bis-styryl-benzothiadiazole (BTD) with carboxylic acid functional groups (X-34/Congo red analog

56 Metabolites are enriched in carboxylic acid functional groups and depleted of ketone

57 -COOH monomer, the nanofibrous structure and carboxylic acid functionalisation of Nano-PEDOT-COOH wer

58 All the materials, except the carboxylic acid functionalised one, offer high PPO loadi

59 ur new VoltageFluor derivatives that possess carboxylic acid functionality for simple conjugation to

60 etraethylene glycol groups terminated with a carboxylic acid functionality were introduced to the CD'

61 bearing three phenol groups and three other carboxylic acid functions, each of these groups on the a

62 nge of 15.6 +/- 3.7 to 70.0 +/- 9.5 nm and a carboxylic acid group density from 0.03 to 0.18 mumol cm

63 It is proposed that the carboxylic acid group directs the isocyanate electrophil

64 was synthesized via an amide linkage between carboxylic acid group of HA and amine group of dopamine.

65 Coordination of the carboxylic acid group to the bulky Mn complex ensures th

66 methyl-substituted alkenes with a hydroxy or carboxylic acid group were thus prepared in 51-97 % yiel

67 ransformation of the isoxazole moiety into a carboxylic acid group, thus opening access to dicarboxyl

68 ter was observed with a surfactant bearing a carboxylic acid group, which anchored amine monomers ver

69 cular orientation via dehydrogenation of the carboxylic acid group, which we confirmed using polariza

70 nity, piperidine-based chemical tags to each carboxylic acid group.

71 ce with a tunable 3D nanofibrous network and carboxylic acid groups (i.e. Nano-PEDOT-COOH) via contro

72 ysis can be explained by the presence of two carboxylic acid groups and a tetracyclic structure.

73 ling with multi-biorecognition molecules via carboxylic acid groups for the development of a range of

74 Furthermore, the carboxylic acid groups provide an anchoring site for the

75 e functionalities, e.g., hydroxy, amino, and carboxylic acid groups, glucuronidation can occur at any

76 e isomeric metabolites each containing three carboxylic acid groups.

77 th excellent tolerance for amide, ester, and carboxylic acid groups.

78 anic compounds by exploiting their pH-active carboxylic acid groups.

79 -4-(perfluoropropan-2-ylidene)cyclopentane-1-carboxylic acid hydrochloride (1) was found to be a sele

80 balance between two opposing effects of the carboxylic acid in the reaction mixture: generation of m

81 d use of "dry ozonolysis" to reveal a masked carboxylic acid in the total synthesis of a natural prod

82 trated for the ligand 4'-hydroxyazobenzene-2-carboxylic acid interacting with avidin protein immobili

83 n was further demonstrated by converting the carboxylic acid into cyclopropyl amine without loss of o

84 hyl-3,4,4a,5,6,7,8,8a-octahydronaphthalene-1-carboxylic acid is a natural product found in Dodonaea v

85 alcohols to their corresponding aldehyde or carboxylic acid is one of the most important classes of

86 talysis by an S-adenosylmethionine-dependent carboxylic acid methyltransferase.

87 ar and charged anchor point residues for the carboxylic acid moiety of the agonist in the interhelica

88 Preservation of the terminal carboxylic acid moiety on ODDA-PTX enables binding to HS

89 zation of substrates bearing an alcohol or a carboxylic acid moiety, is highlighted in the context of

90 to the (1S,2R)-2-(aminomethyl)cyclopentane-1-carboxylic acid monomer precursor, which has a cis-confi

91 ear receptor modulators, which often feature carboxylic acid motifs for target engagement, have emerg

92 6,7,8-tetrahydro-4H-cyclohepta[b]thiophene-3-carboxylic acid o-tolylamide (TM(inh)-23) with 30 nM hal

93 an ester, as the functional precursor to the carboxylic acid of illudinine.

94 terized by a salt bridge between R41 and the carboxylic acid of the inhibitor.

95 p (Z) and at the C-terminus carried either a carboxylic acid or an isophthalic acid (Ipa) anchor grou

96 by free radical processes provide access to carboxylic acid or ketone products.

97 PhFOH/BF(3).OEt(2) even in the presence of a carboxylic acid or primary ammonium group.

98 the substrate, leading to the corresponding carboxylic acid product for the latter, while the former

99 we show the unexplored role of the hydroxyl carboxylic acid receptor type 2 (HCAR2) in 2 models of n

100 eimides, M(p) and M(m), each equipped with a carboxylic acid recognition site, results in the formati

101 alcohol oxidase (AO) or (ii) carboxylic acid/carboxylic acid reductase (CAR) to affect N-alkylation r

102 nonribosomal peptide synthetase (NRPS)-like carboxylic acid reductase (Fub8) in making an aliphatic

103 ated by expanding the substrate scope of the carboxylic acid reductase toward noncognate omega-hydrox

104 ion/transformation of AA to 6-ACA and HMD by carboxylic acid reductases (CARs) and transaminases (TAs

105 They bind with proteins where carboxylic acid residues are dominant ligands.

106 actions are highly charged and often rich in carboxylic acid side chains(1-5), but the structures of

107 2) [II,III] complexes, featuring unprotected carboxylic acid substituents, with Cu(OAc)(2) .

108 of the same 4-substituted Delta1-pyrroline-2-carboxylic acid substrate, making LmbY and GriH unusual,

109 The coupling of an amine with a carboxylic acid to form an amide bond is the most popula

110 Catalytic reduction of carboxylic acid to the corresponding alcohol is a challe

111 Phenanthrene carboxylic acid was detected in the phenanthrene-degradi

112 tween an aryl methyl ether and a neighboring carboxylic acid was developed for creating the chromenon

113 MNPs) coated with poly (pyrrole-co-pyrrole-2-carboxylic acid) (Py/Py-COOH/MNPs) cross-linked with Ab-

114 ecane-1-(methane phosphonic acid)-8-(methane carboxylic acid) and a polyethylene glycol 4 linker, at

115 carbons) and functional groups (sulfonic and carboxylic acid) in zebrafish ( Danio rerio) embryo.

116 2) and VOCs (mainly aldehydes, ketones and a carboxylic acid) were detected as the gaseous products r

117 es (mero166, azide; mero167, alkyne; mero76, carboxylic acid).

118 vel cyclodextrin (CD)-based amphiphilic poly(carboxylic acid)s that self-assemble into highly ordered

119 increase of a contribution of aromatic poly(carboxylic acid)s with high conjugation lengths.

120 deprotection for a substrate that contains a carboxylic acid, a known QD-binding group, is accelerate

121 lear ethylene precursor (aminocyclopropane-1-carboxylic acid, ACC) peak before veraison.

122 ylic acid (tACBC)(n) with N-aminoazetidine-2-carboxylic acid, an 8-helical topology is shown to domin

123 containing compounds, starting from a single carboxylic acid, based on the selection of the nucleophi

124 and simultaneous emission involving coumarin carboxylic acid, furocoumarin and dansyl aniline played

125 with diverse functional groups (i.e. amine, carboxylic acid, isocyanate, alkane and pyridine).

126 alt hydride occurred in the presence of free carboxylic acid, producing the same alkane enantiomer as

127 In combination with the presence of a carboxylic acid, the electronic features of these compou

128 fic chemical moieties, namely, allyl, amine, carboxylic acid, thiol, aldehyde, and catechol, were pre

129 ibe the design, synthesis, and evaluation of carboxylic acid-based ACC inhibitors with organic anion

130 our betalains, named indicaxanthin, indoline carboxylic acid-betacyanin, phenylalanine-betaxanthin, a

131 strategy can be generalized to a variety of carboxylic acid-containing drug structures that satisfy

132 s system (CNS) therapeutics, especially with carboxylic acid-containing drugs.

133 re widely used to decrease volatilization of carboxylic acid-containing herbicides including dicamba.

134 The need for an ester versus carboxylic acid-functionalized coupling partner is also

135 have been developed through the addition of carboxylic acid-functionalized polycarbonate block copol

136 Taken together, carboxylic acid-functionalized polycarbonates represent

137 s, consisting of poly(ethylene oxide) (PEO), carboxylic acid-functionalized polyphosphoester (PPE), a

138 Pyrene carboxylic acid-modified single-walled carbon nanotubes

139 n of reactive intermediates, including mixed carboxylic acid-phosphoric acid anhydrides, for the synt

140 azole moiety as a bioisostere for the distal carboxylic acid.

141 ediated by phenylsilane in the presence of a carboxylic acid.

142 ilable reagents without preactivation of the carboxylic acid.

143 e phenazine derivatives, such as phenazine-1-carboxylic acid.

144 ns bearing a xanthene backbone and a pendant carboxylic acid.

145 the presence of a primary ammonium salt or a carboxylic acid.

146 degrees alcohol/alcohol oxidase (AO) or (ii) carboxylic acid/carboxylic acid reductase (CAR) to affec

147 dihydro-5-(2-methoxyethoxy)-4-oxocinnoline-3-carboxylic acid; Croisor 100) to 27 genotypes in replica

148 -arginine, S-palmitoyl-cysteine, pyrrolidone-carboxylic-acid and SUMOylation sites.

149 -based complex, treatment of a hydroxy- or a carboxylic-acid-containing olefin with commercially avai

150 simultaneously transformed to perfluoroalkyl carboxylic acids (C2-C7 PFCAs) of different chain length

151 s (furfural and 5-hydroxymethylfurfural) and carboxylic acids (lactic acid, succinic acid, fumaric ac

152 Medium-chain carboxylic acids (MCCAs) are valuable platform chemicals

153 Perfluoroalkyl carboxylic acids (PFCA) in snowpacks display odd-even co

154 Several linear chain perfluoroalkyl carboxylic acids (PFCAs) (C4 to C7) were identified as b

155 ride and sulfate, short-chain perfluorinated carboxylic acids (PFCAs) were identified and quantified

156 yl sulfonic acids (PFSAs) and perfluoroalkyl carboxylic acids (PFCAs) were readily degraded, other st

157 redictor of the enrichment of perfluoroalkyl carboxylic acids (PFCAs) with >=7 perfluorinated carbons

158 oefficients, K(mem/w), of six perfluoroalkyl carboxylic acids (PFCAs), three perfluoroalkanesulfonic

159 lfonates (PFSAs, C(4-12)), 10 perfluoroalkyl carboxylic acids (PFCAs, C(4-13)), and perfluorooctane s

160 ge: 1-110 ng/g) and two perfluorinated ether carboxylic acids (PFO(4)DA and PFO(5)DoDA; PFO(5)DoDA ra

161 PFAA congeners, summation of perfluoroalkyl carboxylic acids (SigmaPFCAs), and SigmaPFAAs correlated

162 ess, probably owing to differences in target carboxylic acids (which can bind to the aniline (AN) m-a

163 his deterrence is based on the feces-emitted carboxylic acids 3-methylpentanoic acid and hexanoic aci

164 oxidants for the construction of esters from carboxylic acids and alcohols in the presence of stoichi

165 NMVOCs were largely dominated by small carboxylic acids and alcohols, and furans.

166 In these films, residual carboxylic acids and amines influence permeability and s

167 cross-coupling of vinyl boronic esters with carboxylic acids and aryl iodides is described.

168 tereoisomers of tetrasubstituted azetidine-2-carboxylic acids and derivatives that possess three chir

169 d NSSM, respectively, which mainly belong to carboxylic acids and derivatives, polyketides and fatty

170 sing the measured (-)ESI efficiencies of the carboxylic acids and dimer esters as more representative

171 ity of the reaction in the presence of other carboxylic acids and its utility in the functionalizatio

172 ncluded amino acids, fatty acid derivatives, carboxylic acids and phenolic compounds.

173 tural sources and consumer products, such as carboxylic acids and plasticizers.

174 xidation of residual carbon atoms first into carboxylic acids and then volatile carbon species, while

175 d variants often require a pre-activation of carboxylic acids and/or employment of costly transition-

176 Aromatic carboxylic acids are found to undergo reactions with iso

177 Ethers derived from C(2) and C(4) carboxylic acids are identified as advantaged fuel candi

178 These renewable carboxylic acids are involved in the synthesis of releva

179 he developed methodology rendered the use of carboxylic acids as a direct surrogate of primary amines

180 The reaction uses naturally abundant organic carboxylic acids as carbon sources, readily prepared azi

181 An alternative approach is to use ubiquitous carboxylic acids as starting materials and perform a dec

182 commodates a large variety of heteroaromatic carboxylic acids as well as olefins, and facilitates a d

183 DFT studies, aided by crystal structures of carboxylic acids bound by the catalyst, point to a plaus

184 chromones, 3-formylchromones, and chromone-3-carboxylic acids by means of visible-light photoredox ca

185 nyl complexes, a chelator was selected whose carboxylic acids can easily be converted into various de

186 hat a Mn-catalyzed C-H oxidation directed by carboxylic acids can overcome these challenges to yield

187 ce of two alpha-methyl groups; (2) aliphatic carboxylic acids containing alpha-hydrogens are compatib

188 s for enantiodiscrimination of alpha-racemic carboxylic acids containing tertiary or quaternary stere

189 method allows unprecedented direct access to carboxylic acids derived from beta,beta-trisubstituted a

190 Protein backbones and pyridine-carboxylic acids dominated this discrimination and might

191 and epsilon-lactonization reactions of free carboxylic acids enabled by a novel cyclopentane-based m

192 Our results show that carboxylic acids enhance the OP(AA) and OP(*OH) by TMs w

193 se-catalyzed chemoselective hydroboration of carboxylic acids has been developed with a high turnover

194 Different types of carboxylic acids have been included in this review: mono

195 of endocyclic enol lactones from unsaturated carboxylic acids in an one-pot procedure.

196 and NRPS-like enzymes activate and transform carboxylic acids in both primary and secondary metabolis

197 h cis- and trans-1,3-disubstituted housane-1-carboxylic acids in diastereoselective manner on up to 8

198 s and enantioselectivities, affording chiral carboxylic acids including Naproxen, (S)-Flurbiprofen, a

199 synthesis of COO-BODIPYs from F-BODIPYs and carboxylic acids is established.

200 oach to the carbon-14 radiolabeling of alkyl carboxylic acids is presented.

201 and hydroalkenylation of unactivated alkenyl carboxylic acids is reported, whereby the ligand environ

202 catalysis (BAC), electrophilic activation of carboxylic acids leads to the formation of amides from a

203 nd used for classification of wines based on carboxylic acids levels, which were indirectly related t

204 Naphthenic acids (NAs) are carboxylic acids naturally occurring in crude oils and b

205 Starting with a mixture of activated carboxylic acids of different lengths, iterative cycling

206 reased over time, and >=C(11) perfluorinated carboxylic acids only seem to level off during the last

207 have shown that introducing large amounts of carboxylic acids or ammonium hydroxide to LC eluents pos

208 ed into an aldehyde or ketone (for instance, carboxylic acids or organic carbonate or nitriles) or in

209 lationship (SAR) of antischistosomal ozonide carboxylic acids OZ418 (2) and OZ165 (3).

210 Enzymes that cleave ATP to activate carboxylic acids play essential roles in primary and sec

211 alkylation of amines with either alcohols or carboxylic acids represents a mild and safe alternative

212 nessed to activate nucleoside phosphates and carboxylic acids through catalysis by acid and 4,5-dicya

213 The addition of carboxylic acids to allenes was performed with copper ca

214 ed the gamma-C(sp(3) )-H olefination of free carboxylic acids to form diverse six-membered lactones.

215 A method for the annulation of amines and carboxylic acids to form pharmaceutically relevant azahe

216 ght in the presence of acetic acid and other carboxylic acids to generate methyl and alkyl radicals,

217 The method is based on conversion of carboxylic acids to the corresponding organic halides vi

218 production of short-chain alkanes from waste carboxylic acids under mild reaction conditions.

219 e N-acylation of glycosamine with a range of carboxylic acids under physiological reaction conditions

220 cert to decarboxylate alpha-beta unsaturated carboxylic acids using a highly modified flavin cofactor

221 carboxylative functionalization of aliphatic carboxylic acids using N-xanthylamides.

222 tric hydrogenation of alpha,beta-unsaturated carboxylic acids using readily prepared bis(phosphine) c

223 ides using the deoxofluorination reaction of carboxylic acids using XtalFluor-E is described.

224 of N-hydroxyimides with ketones, esters, and carboxylic acids was achieved employing the di-tert-buty

225 s and (alpha,beta-unsaturated) nitriles from carboxylic acids was realized through oxidative decarbox

226 initial formation of the Castagnoli-Cushman carboxylic acids was shown to be the case, and their dec

227 fully synthesized, and no over-oxidations to carboxylic acids were detected.

228 The oxidative coupling of carboxylic acids with liquid ketones and cyclic ethers h

229 one single step, the desired carbon tag into carboxylic acids with no need of structural modification

230 luorination of cinnamic and (hetero)aromatic carboxylic acids with sulfur tetrafluoride.

231 , catalyzing the transvinylation reaction of carboxylic acids without losing their original metatheti

232 s relies upon one high-availability reagent (carboxylic acids) and one low-availability reagent (orga

233 e present in HULIS, oxygen-containing (i.e., carboxylic acids) and reduced-nitrogen-containing organi

234 amine group ( N-acylation with aldehydes and carboxylic acids).

235 ) values of phenols, aliphatic, and aromatic carboxylic acids, and ketoacids.

236 s revealed methyl ketones, alcohols, esters, carboxylic acids, and nitrogen- and sulfur-containing co

237 carbonyl derivatives, such amides, ester and carboxylic acids, are presented in a systematic manner.

238 alyzed conjunctive cross-coupling of alkenyl carboxylic acids, aryl iodides, and aryl/alkenyl boronic

239 turated aliphatic hydrocarbons, esters, free carboxylic acids, as well as minor amounts of amides and

240 Besides alkyl carboxylic acids, benzylic C(sp(3) )-H bonds also could

241 cyclic and heterocyclic amines directly with carboxylic acids, by-passing their preactivation as redo

242 Herein we report that pendant carboxylic acids, combined with bulky monophospine ligan

243 droxyphenyl)propanoic and 5-oxopyrrolidine-2-carboxylic acids, diacetyl, acetoin, and an unidentified

244 provide the transport steps for amino acids, carboxylic acids, fatty acids, cofactors, inorganic ions

245 ylate a wide range of aromatic and aliphatic carboxylic acids, have multiple reusability, and are a r

246 is accepting of a broad scope of alkene and carboxylic acids, including challenging ones that produc

247 is displayed, and application of a range of carboxylic acids, including secondary alpha-amino acids,

248 al group tolerance (phenols, amides, ethers, carboxylic acids, ketones, and acrylic esters).

249 Thus, carboxylic acids, once converted to redox-active esters

250 of amino acids, as well as into alcohols and carboxylic acids, rapidly and in excellent yields, using

251 remote C-H activation reactions of alcohols, carboxylic acids, sulfonates, phosphonates, and amines.

252 Aliphatic alcohols, phenols, carboxylic acids, thiols and sulfonamides were found to

253 ion in the number of glomeruli responding to carboxylic acids-chemicals associated with microbial act

254 l azoliums for the formation of ketones from carboxylic acids.

255 ding aldehydes, ketones, esters, amides, and carboxylic acids.

256 es used for amide bond synthesis: amines and carboxylic acids.

257 H substrates, such as unactivated esters and carboxylic acids.

258 lity of Kochi's oxidative decarboxylation of carboxylic acids.

259 which further undergoes amide coupling with carboxylic acids.

260 iberate high-energy carbocations from simple carboxylic acids.

261 naerobically digested to produce short-chain carboxylic acids.

262 ons and conjugate additions with unsaturated carboxylic acids.

263 used as coupling partners to provide chiral carboxylic acids.

264 d and 2d did not give the corresponding C(3)-carboxylic acids.

265 ate as an oxidizing agent for perfluoroalkyl carboxylic acids.

266 mary alcohols in lignin to the corresponding carboxylic acids.

267 and selective synthesis of hydrocarbons from carboxylic acids.

268 e NAD(+)-dependent oxidation of aldehydes to carboxylic acids.

269 parent acid, thus providing a route to many carboxylic acids.

270 xidation of aldehydes to their corresponding carboxylic acids.

271 phile classes, including azoles, amines, and carboxylic acids.

272 ytic processes for producing biomass-derived carboxylic acids.

273 H olefination of ketone derivatives and free carboxylic acids.

274 g the palladium-catalyzed alpha-arylation of carboxylic aids and secondary amides with aryl halides.

275 Ratios of carboxylic and hydroxylic terminating groups, which are

276 tion of flavonol aglycones to phloroglucinol carboxylic and phenolic acids.

277 gonally protected 1,4-diamine, epsilon-amino carboxylic, and epsilon-amino ketone derivatives.

278 with SO(3) and form the ion pair of sulfuric-carboxylic anhydride and hydronium.

279 mides as fuels to generate transient aqueous carboxylic anhydrides has recently been used in examples

280 Carboxylic (COOH), carbonyl (C=O), and hydroxyl (OH) gro

281 ly nucleophilic coupling partners with other carboxylic derivatives (to produce ketones), imines (to

282 d residue (~1396 cm(-1)), and C=O stretching carboxylic esters (1745 cm(-1)).

283 ees C) leads to the formation of isoxazole-4-carboxylic esters and amides in good yields.

284 er-catalyzed gamma-alkylation of phthalide 3-carboxylic esters has been developed, giving access to 3

285 d for converting (3-methyloxetan-3-yl)methyl carboxylic esters into 3-thiomethyltetrazines.

286 Carbonyl, phenolic, and carboxylic functional groups in the unreacted samples we

287 ly due to the complexation of VO(2+) ions by carboxylic functions at the interface between bitumen an

288 between the skeleton of the molecule and the carboxylic group and the liberation of carbon dioxide.

289 e hydrogen bonds between the ligand proximal carboxylic group and the main chain of two conserved loo

290 ation of the hydroxylated carbon 1 to give a carboxylic group by TcADH2 and TcALDH1, the same enzymes

291 successive oxidation of carbon 10 (C10) to a carboxylic group by TcCHH, a cytochrome P450 oxidoreduct

292 ed that such sugar derived acids with active carboxylic groups could cause instability in products ri

293 tensities higher than those corresponding to carboxylic groups in samples from the supernatant from b

294 (ii) by formation of the amide bonds between carboxylic groups of rGO-Fc(COOH)(2) and amine groups fr

295 of membranes with a greater concentration of carboxylic groups so that it was negative across the ent

296 howed that alcoholic groups are converted to carboxylic groups while reducing Cr (VI) to Cr (III).

297 h DOM constituents with different amounts of carboxylic groups.

298 richment levels (up to an average of 46% per carboxylic oxygen).

299 hod uses carbodiimide chemistry to footprint carboxylic residues, whereby 1-ethyl-3-(3-(dimethylamino

300 eagents exhibiting acidic functional groups (carboxylic, sulfonic), which become deprotonated and neg