ライフサイエンスコーパス: carboxylic acid

1 ite) and an amino acid analogue (azetidine-2-carboxylic acid).

2 n of the resulting C1 primary alcohol to the carboxylic acid.

3 and the ethylene precursor aminocyclopropane-carboxylic acid.

4 c C-O bond cleavage to release an alcohol or carboxylic acid.

5 xyl ring and/or the electronic effect of the carboxylic acid.

6 sence of a long-chain amine and a long-chain carboxylic acid.

7 -methoxybenzyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid.

8 id hydrolysis of the ester into the inactive carboxylic acid.

9 electronically different substituents on the carboxylic acid.

10 xylated, beta-fluorinated, and beta-arylated carboxylic acids.

11 riegated building blocks of chemistry: alkyl carboxylic acids.

12 with dicarbonyls, hydroxycarbonyls, and oxo-carboxylic acids.

13 ge in regioselectivity and form unconjugated carboxylic acids.

14 from those observed for sulfones or aromatic carboxylic acids.

15 derivatives are better protective groups for carboxylic acids.

16 vated Ascaris eggs through exposure to these carboxylic acids.

17 d urea units achieves this goal with hydroxy carboxylic acids.

18 l is suitable for many primary and secondary carboxylic acids.

19 y important derivatives such as nitriles and carboxylic acids.

20 thiol-ene modification to introduce pendant carboxylic acids.

21 erification of amides derived from aliphatic carboxylic acids.

22 ickel complex that couples aryl halides with carboxylic acids.

23 O2 (44 Da) and C2H6O2Si (90 Da) for aromatic carboxylic acids.

24 eactions using H2O2 in the presence of added carboxylic acids.

25 s an intermediate to the final conversion to carboxylic acids.

26 rated by synthesizing several derivatives of carboxylic acids.

27 before their fermentation into alcohols and carboxylic acids.

28 decarboxylation of redox-activated aromatic carboxylic acids.

29 t oxidation of aldehydes to their respective carboxylic acids.

30 rs, anti-1-amino-3-(18)F-fluorocyclobutane-1-carboxylic acid ((18)F-FACBC or (18)F-fluciclovine) has

31 (18)F-labeled 1-amino-3-fluorocyclobutane-1-carboxylic acid ((18)F-fluciclovine) is a leucine analog

32 atile fraction mainly contains esters (38%), carboxylic acids (19%), aldehydes (11%), alcohols (14%),

33 by (2S,4R)-4-(2-carboxyphenoxy)pyrrolidine-2-carboxylic acid (1b), for cloned homomeric kainic acid r

34 erivative cis-2-(carboxymethyl)cyclohexane-1-carboxylic acid [(1R,2R)-/(1S,2S)-2-(carboxymethyl)cyclo

35 n-6-amine (LY2784544) and 1H-benzimidazole-4-carboxylic acid, 2-methyl-1-[[2-methyl-3-(trifluoromethy

36 Carboxylic acids, 2-furaldehyde, 5-hydroxymethyl-2-fural

37 e, 1 [Ga(tpfc)], with either sulfonic (2) or carboxylic acids (3, 4) as macrocyclic ring substituents

38 amides, (2) hydrolysis of N-methoxyamides to carboxylic acids, (3) metal- and oxidant-free benzocouma

39 ion of 3-((furan-2-ylmethyl)amino)pyridine-4-carboxylic acid 34 and 3-(((3-methylthiophen-2-yl)methyl

40 -methylthiophen-2-yl)methyl)amino)pyridine-4-carboxylic acid 39 that are inhibitors of the KDM4 (JMJD

41 )-5-ethyl-1,6-dihydroxycyclohexa-2,4-diene-1-carboxylic acid (4) into compound 3, the latter being a

42 oughout the colony, with 5-methylphenazine-1-carboxylic acid (5-MCA) and pyocyanin (PYO) localized to

43 ic acid analog 7-chloro-4-oxo-1H-quinoline-2-carboxylic acid (7-chlorokynurenic acid; 7-CKA).

44 (hexanal, pentenal, nonanal and nonenal) and carboxylic acids (9-oxononanoic acid, octanoic acid, non

45 For carboxylic acids a sharp increase in sensitivity is like

46 tetramers) of cis-2-(aminomethyl)cyclobutane carboxylic acid, a gamma-amino acid featuring a cyclobut

47 4,5-dihydroxy-2,3,4,5-tetrahydropyridazine-3-carboxylic acid, a gamma-halogenated piperazic acid, and

48 t was modified by moving the position of the carboxylic acid, a key pharmacophore for GPR40.

49 Only protonated analytes with a carboxylic acid, a sulfone, or a sulfonamide functionali

50 The toxicity of azetidine-2-carboxylic acid (A2C), a structural analogue of L-prolin

51 of this regulation is 1-aminocyclopropane-1-carboxylic acid (ACC) synthases (ACS), generally the rat

52 alicylic acid (SA) and 1-aminocyclopropane-1-carboxylic acid (ACC) were ineffective.

53 enosyl-L-methionine to 1-aminocyclopropane-1-carboxylic acid (ACC)] and PsACO (encode enzymes that co

54 t added acid due to the in situ formation of carboxylic acids, accounting for the long-known catalyti

55 no-2-carboxyethyl]-4,5-dihydro-1H-pyrazole-3-carboxylic acid (ACEPC) competitive GluN2 antagonists, o

56 ion, and the reaction is amenable to in situ carboxylic acid activation.

57 ) and P(2-MeOPh)3 (2 mol%), sterically tuned carboxylic acid additives, and an environmentally friend

58 We observed that uncharged carboxylic acids affected viability rather than the pH i

59 produces polyfunctional low molecular weight carboxylic acids after oxidative cleavage of the aromati

60 produced several volatile compounds, such as carboxylic acids, alcohols, aldehydes and ketones.

61 igid arylated derivatives or flexible linear carboxylic acids, alcohols, olefins and amines in both m

62 rbonyl radiopharmaceuticals based on labeled carboxylic acids, amides, carbamates and ureas now accou

63 ere readily converted into primary alcohols, carboxylic acids, amides, isocyanates, and carbamates, a

64 Cross-metathesis with olefins that contain a carboxylic acid, an aldehyde, an allylic alcohol, an ary

65 mentation of the resulting oxyanion into the carboxylic acid and a benzyl anion.

66 leads to the formation of the corresponding carboxylic acid and alcohol.

67 The reaction displays a broad scope of carboxylic acid and alkyne coupling partners, and can to

68 r, KAHA, KATs, etc.) that could involve both carboxylic acid and amine surrogates are treated separat

69 g biocatalysts for amide bond formation from carboxylic acid and amine.

70 on of a variety of alpha-hydrogen-containing carboxylic acid and amino acid-derived amides.

71 during growth on a physiologically relevant carboxylic acid and at elevated temperatures.

72 catalysis, to extract carbon dioxide from a carboxylic acid and economically replace it with an orga

73 nantiomers of 2-amino-3-hydroxycyclobutane-1-carboxylic acid and of 2-amino-4-hydroxycyclobutanecarbo

74 unctional groups in these molecules, such as carboxylic acid and phenol moieties, become deprotonated

75 An optimized route to enantiopure tetra-carboxylic acid and tetra-carboxamide bis(diazaphosphola

76 tones were the most efficient stimuli, while carboxylic acids and aliphatics/aromatics were comparati

77 )-catalyzed Heck-type coupling between arene carboxylic acids and alkenes at room temperature.

78 ation of sp(3)-sp(3) bonds using only simple carboxylic acids and alkyl halides as the nucleophilic a

79 m of the zirconium-catalyzed condensation of carboxylic acids and amines for direct formation of amid

80 AD(P)(+)-dependent oxidation of aldehydes to carboxylic acids and are important for metabolism and de

81 (1a-e) were derived from their corresponding carboxylic acids and bidentate directing groups.

82 enerable Suzuki cross-coupling between alkyl-carboxylic acids and boronic acids is described.

83 to amino acids, peptides and carbohydrates, carboxylic acids and compatible solutes may be essential

84 investigated linear peroxy acids but not for carboxylic acids and could therefore serve as a diagnost

85 essible through reactions between ubiquitous carboxylic acids and coupling agents widely used in amid

86 es two GRNs that respond only to a subset of carboxylic acids and high concentrations of salt.

87 probe to enable rapid quantification of both carboxylic acids and hydroperoxides in hydrocarbon sampl

88 Higher alcohols, carboxylic acids and ketones gradually increased during

89 Commonly used anchors such as carboxylic acids and phosphonic acids have limited stabi

90 Aliphatic carboxylic acids and sulfonamides could not be different

91 Both aliphatic carboxylic acids and sulfonamides yield several fragment

92 tional methanol elimination was observed for carboxylic acids and sulfonamides.

93 ylates from Se/LiEt3BH and acyl chlorides or carboxylic acids and their reaction with sugar azides.

94 is fast at acidic pH and tolerates alcohols, carboxylic acids, and even secondary amines in the subst

95 mposition routes for furanoids and aliphatic carboxylic acids, and mechanistic pathways for the radio

96 clopentylation" of amines, alcohols, thiols, carboxylic acids, and other heteroatoms is introduced.

97 nated PAMAM dendrimers, we confirm safety of carboxylic acid- and pyrrolidone-terminated PAMAM dendri

98 Notably, aryl carboxylic acids are isolated by simple filtration techn

99 how that low molecular weight and oligomeric carboxylic acids are kinetically equivalent at accelerat

100 Carboxylic acids are present in many foods, being especi

101 Alkyl carboxylic acids are ubiquitous in all facets of chemica

102 Gas-phase carboxylic acids are ubiquitous in ambient air, yet thei

103 Lithium enolates derived from carboxylic acids are ubiquitous intermediates in organic

104 ionalization of the beta-C(sp(3))-H bonds of carboxylic acids are well documented, but only a few rep

105 iscovery of 2-acylaminocycloalkylthiophene-3-carboxylic acid arylamides (AACTs) as inhibitors of TMEM

106 In contrast, the use of chiral carboxylic acids as Bronsted acid catalysts is much less

107 The degradation reaction yielded C1-C4 carboxylic acids as the final products.

108 reaction relies upon the activation of alkyl carboxylic acids as their redox-active ester derivatives

109 on of primary, secondary, and tertiary alkyl carboxylic acids as well as a diverse range of natural-p

110 oduced by oxidation of 1-aminocyclopropane-1-carboxylic acid, as catalyzed by 1-aminocyclopropane-1-c

111 We then showed that carboxylic acids at these concentrations inactivated Asc

112 of the hydrazone to a mixture of oxidant and carboxylic acid avoids the buildup of the diazo compound

113 ures show that vegetable-sourced azetidine-2-carboxylic acid (Aze), a dual mimic of proline and alani

114 h analogues of varying ring sizes (azetidine carboxylic acid, Aze, and piperidine carboxylic acid, Pi

115 sive polymers classified as polyacids (e.g., carboxylic acid based polymers, sulfonamides, anionic po

116 her and also from sulfonamides and aliphatic carboxylic acids based on reactions with TMMS and one or

117 surfaces by pre-attaching probe molecules to carboxylic acid bearing termonomers of pyrrole phenylene

118 2-(5-bromo-2-hydroxy-phenyl)-thiazolidine-4-carboxylic acid (BHTC).

119 be system based on 4'-substituted biphenyl-2-carboxylic acids (BPAs) for analysis of photooxidants ge

120 -methoxybenzyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (BQCA) (1), but markedly improved positi

121 restored by treatment with benzyl quinolone carboxylic acid (BQCA) and benzoquinazoline-12 (BQZ-12),

122 for constructing amide bonds join amines and carboxylic acids by dehydrative couplings-processes that

123 hnique for selective fluorination of various carboxylic acids by exposure to gaseous sulfur tetrafluo

124 phoresis, as well as the separation of small carboxylic acids by gradient elution moving boundary ele

125 Direct amidation of carboxylic acids by reaction with amines in the presence

126 In summary, sulfones and aromatic carboxylic acids can be differentiated from each other a

127 of judicious catalyst design, the acidity of carboxylic acids can be modulated, for instance by stabi

128 tion approach, is especially useful in rapid carboxylic acid carbon isotope labeling, however develop

129 studies of six Ru polypyridyl compounds with carboxylic acid/carboxylate group(s) revealed that some

130 an, but not 2-aminobicyclo-(2,2,1)-heptane-2-carboxylic acid, competitively inhibited (11)C-sarcosine

131 y of Ascaris eggs as a function of uncharged carboxylic acid concentration for n-butyric acid and n-c

132 A negative rate dependence on carboxylic acid concentration is observed along with S-s

133 angement was also shown for the triarylamine-carboxylic acid conjugate.

134 y have described highly potent and selective carboxylic acid containing MMP-13 inhibitors; however, n

135 pH/proton concentration and the structure of carboxylic acids contribute to sour GRN activation.

136 sensitivity to functional group addition is carboxylic acid (COOH) approximately hydroxyl (OH) > nit

137 eophilic groups on Wnt proteins to activated carboxylic acid (COOH) or glutaraldehyde (COH) groups fu

138 Selected carboxylic acids could be converted to their correspondi

139 f the beta2AR bound to a polyethylene glycol-carboxylic acid derivative (Cmpd-15PA) of this modulator

140 ve the decarboxylative coupling of aliphatic carboxylic acid derivatives (specifically, readily avail

141 akin-West reaction of advanced pyrrolidine 2-carboxylic acid derivatives that can be assembled stereo

142 kyl-5-aryl/alkyl/methoxycarbonyl-1H-pyrrol-3-carboxylic acid derivatives typically under mild conditi

143 ivated enamides, known as the least reactive carboxylic acid derivatives, toward alkylation with orga

144 for the construction of fluorine-containing carboxylic acid derivatives.

145 nient precursor to access various conjugated carboxylic acid derivatives.

146 se inhibitor and 4-amino-tetrahydropyranyl-4-carboxylic acid derived dipeptide GSK-2793660, which is

147 two bioactive peptides: 2-aminoadamantane-2-carboxylic acid derived P2X7-evoked glutamate release in

148 Acyl groups with >2 carboxylic acids diminished self-assembly into ThT-posit

149 rther, we report the first example of a free carboxylic acid-directed Pd(II)-catalyzed C(sp(3))-H bro

150 res a scalable classical resolution of tetra-carboxylic acid enantiomers with recycling of the resolv

151 an optical pH indicator, SNARF-5F, 5-(and-6)-Carboxylic Acid, encapsulated into polyacrylamide nanopa

152 est alkyl chain, -(CH2)2-, and a hydrophilic carboxylic acid end group are found to be the most effec

153 )-1-methyl-4-nitro-3,5-diphenylpyrrolidine-2-carboxylic acid (endo-6) and (2S,3S,4R,5S)-1-methyl-4-ni

154 -methoxybenzyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid, enhanced acetylcholine-mediated phospho

155 the one-pot preparation of alpha-quaternary carboxylic acids, esters, and amides with a high degree

156 )-1-methyl-4-nitro-3,5-diphenylpyrrolidine-2-carboxylic acid (exo-6), combined with 1,8-diazabicyclo[

157 The bipedal walker has identical carboxylic acid feet, and "steps" along an isotactic hyd

158 ion of (hetero)cyclic alpha,beta-unsaturated carboxylic acids from 1,6- and 1,7-enyes and CO2.

159 the synthesis of certain phenyl-substituted carboxylic acids from 2-phenylcycloalkanones.

160 , while in biochar was featured by saturated carboxylic acids from hemi/cellulose and lipids with con

161 ctors was primarily due to 5:3 fluorotelomer carboxylic acid (FTCA - 3.9 nmol/L) and perfluorohexanoi

162 landfill leachate samples, 5:3 fluorotelomer carboxylic acid (FTCA) was dominant and variations in co

163 tionally apply isosteric replacements of the carboxylic acid functional group.

164 ), titanium dioxide nanofibers (TiO2NFs) and carboxylic acid functionalized multi-walled carbon nanot

165 sor design involves disposable devices using carboxylic acid-functionalized magnetic microparticles s

166 We find that the carboxylic acid group deprotonates at a significantly hi

167 ins are folded in a hairpin manner near each carboxylic acid group, giving rise to multiple embedded

168 by probing the vibrational signatures of the carboxylic acid group, representing the nondissociated a

169 Hydrogels consisting of carboxylic acid groups and N-isopropylacrylamide as pend

170 itive case of a hydrogel containing multiple carboxylic acid groups at each crosslinking point in the

171 While its two carboxylic acid groups can be readily utilized in connec

172 sorbent coating featuring halide anions and carboxylic acid groups in the cationic portion exhibited

173 The polymer P3 contains a lot of carboxylic acid groups on its surface that provide a lar

174 precise linear architecture, namely, pendant carboxylic acid groups precisely every 21st backbone car

175 to the porphyrin and proton transfer from a carboxylic acid hanging group or an external acid to the

176 on of 8-methylquinoline to the corresponding carboxylic acid has also been noted at Pd(II).

177 bly between a phosphoric acid catalyst and a carboxylic acid has recently been established as a new a

178 catalyzed amino lactonization of unsaturated carboxylic acids has been achieved as well as the analog

179 ormal two-carbon scission of allyl groups to carboxylic acids has been developed.

180 ediated cleavage of ketones into alkanes and carboxylic acids has been reinvestigated and the substra

181 ,2R)-/(1S,2S)-2-(carboxymethyl)cyclohexane-1-carboxylic acid] has previously been identified as metab

182 c(NN) is 2-amino-5-nitronylnitroxide-indan-2-carboxylic acid, have been inserted at positions i and i

183 A functional group such as an amide, carboxylic acid, imidazole, or phenol appeared to negati

184 diazole and alpha,alpha-dimethylation of the carboxylic acid, improving DGAT1 potency and gut permeab

185 ogenous phenazines pyocyanin and phenazine-1-carboxylic acid in both cytosolic and membrane fractions

186 ctional groups on the beta-carbon (e.g., the carboxylic acid in glycine) that facilitate carbon-carbo

187 ntioenriched amides, unactivated esters, and carboxylic acids in a one-pot manner.

188 dicate that in situ biological production of carboxylic acids in HFM provides a promising method of p

189 To fill this gap, we measured gas-phase carboxylic acids in real-time inside and outside of a un

190 les-derived from Fukuyama amines-and peptide carboxylic acids in Ugi and Passerini reactions to affor

191 ce (hydrolytically unstable) anhydrides from carboxylic acids in water.

192 l-5 -yl)-[1,1'-biphenyl]-4-yl)cyclopropane-1-carboxylic acid) in rhesus monkeys to image LPA1 in the

193 Carboxylic acid incorporation into parent MWO hydrocarbo

194 ate-stage C-H functionalization converting a carboxylic acid into a lactone through the oxidation of

195 is a classic, powerful method for converting carboxylic acids into protected amines, but its widespre

196 The conversion of widely available carboxylic acids into versatile boronic esters would be

197 ethanolamine scaffold containing a terminal carboxylic acid is described.

198 erminal and substituted alkynes from various carboxylic acids is described using both nickel- and iro

199 y fluorodecarboxylation of the corresponding carboxylic acids is reported.

200 (2-(2-carboxyethyl)-4-methyl-5-propylfuran-3-carboxylic acid) is a metabolite that circulates at high

201 e (LND; 1-(2,4-dichlorobenzyl)-1H-indazole-3-carboxylic acid) is known to interfere with energy-yield

202 In conversions with ferrocene carboxylic acids, isocyanates provide imides in good yie

203 essment of the physicochemical properties of carboxylic acid isosteres would be desirable to enable m

204 ovel and efficient method for alkyl and aryl carboxylic acid isotopic labeling using a single reagent

205 pH2cH = 2,2'-bipyridine-6-phosphonic acid-6'-carboxylic acid, L = 4-picoline or isoquinoline) catalys

206 otency and pharmacokinetic properties of non-carboxylic acid leads resulting in the identification of

207 In addition, some carboxylic acids measured indoors correlated to CO2 in d

208 While carboxylic acids measured outdoors displayed a single da

209 The campaign-average concentration of carboxylic acids measured outdoors was 1.0 ppb, with the

210 is due to the presence of negatively charged carboxylic acid moieties from PAA grafts that electrosta

211 ed SPME sorbent coatings, the PIL containing carboxylic acid moieties in the monomer and halide-based

212 a known azetidine FFA2 antagonist, we used a carboxylic acid moiety known not to be critical for rece

213 icyclic nortropine-substituted benzothiazole carboxylic acid moiety onto a trisubstituted isoxazole s

214 inciple as amide bond formation to replace a carboxylic acid moiety with a boronate ester.

215 ne-pot synthesis of thioesters directly from carboxylic acids, N,N'-diphenylthiourea, triethylamine,

216 phorylated and N-acetylated sugars, polyols, carboxylic acids, nucleotides, and amines.

217 This implies a key role in binding for the carboxylic acid of the fatty acid.

218 D-amino acid substrate was linked to the carboxylic acid on the magnetic nanoparticles using EDC/

219 etathesis of silylated alkynes with aromatic carboxylic acids on the Ag(111) and Au(111) surfaces to

220 able N-substituted amides or their requisite carboxylic acids or acid chlorides have been used to con

221 nd with the acceptor groups varied as either carboxylic acids or benzoic acids on the pi-bridge.

222 N bond to release the corresponding alcohol, carboxylic acid, or amine when an electron-donating amin

223 ining an alcohol, an aldehyde, an epoxide, a carboxylic acid, or an alkenyl group may be used.

224 essing the activity of 1-aminocyclopropane-1-carboxylic acid oxidase (ACO), the enzyme catalysing the

225 acid, as catalyzed by 1-aminocyclopropane-1-carboxylic acid oxidase.

226 .g., with no pre- or in situ activation of a carboxylic acid partner) approaches for the construction

227 oduction reveals distribution of phenazine-1-carboxylic acid (PCA) throughout the colony, with 5-meth

228 enazine pyocyanin and the yellow phenazine-1-carboxylic acid (PCA).

229 ) and measured contents of FBPs (pyrrolidone carboxylic acid [PCA] and urocanic acid [UCA]) using UPL

230 UnDA, representing long-chain perfluoroalkyl carboxylic acids (PFCAs), showed a more homogeneous spat

231 acids (PFSAs; C4,6,8,10) and perfluoroalkyl carboxylic acids (PFCAs; C6-15) along with six perfluoro

232 id (FTCA - 3.9 nmol/L) and perfluorohexanoic carboxylic acid (PFHxA - 2.9 nmol/L).

233 and significant generation of perfluoroalkyl carboxylic acid (PFOA) at a yield of 30 mol % by day 180

234 etidine carboxylic acid, Aze, and piperidine carboxylic acid, Pip) to produce different trans/cis rat

235 nduce radical fragmentation reactions in the carboxylic acid polyether ionophore nigericin.

236 s by methylation of alcohol, thiol, amine or carboxylic acid precursors using [(11)C]methyl iodide or

237 Alcohols and carboxylic acids preferentially captured thiiranium ions

238 o]phenyl]-5-(trifluoromethyl)-1H-p yrazole-4-carboxylic acid prevents AIAD in mice, (2) TRPC3 channel

239 adenylation of substrates, amidation of the carboxylic acid proceeds by direct reaction of the acyl

240 peroxide anion 7' to afford the aldehyde-to-carboxylic acid product or as a hydroperoxy derivative 7

241 unmask net beta,gamma-dicarbofunctionalized carboxylic acid products.

242 Further studies of carboxylic acid promoted dye isomerization in heptane an

243 d donors and chiral phosphoric acids, chiral carboxylic acids provide the opportunity to activate a d

244 (MNPs) coated with poly(pyrrole-co-pyrrole-2-carboxylic acid) (Py/Py-COOH) for high efficient detecti

245 (primary alcohol, phenol, vicinal diol, and carboxylic acid), ranging in complexity from methanol to

246 hat differ in the relative position of their carboxylic acid recognition site: either para (M(p)) or

247 Carboxylic acid reductases (CARs) catalyze the reduction

248 aratus of BT3686 does not comprise a pair of carboxylic acid residues but, uniquely, a single histidi

249 mistry has been developed for aryl and alkyl carboxylic acids respectively with two rationally design

250 ted as potential photocages for alcohols and carboxylic acids, respectively.

251 posing oleate-capped quantum dots to primary carboxylic acids results in a one-for-one exchange that

252 for decarboxylative fluorination of several carboxylic acids showcases the performance of the comple

253 acrylamide, and series III with a saturated carboxylic acid substituent.

254 ,6,6-tetramethyl-piperidine-1-oxyl-4-amino-4-carboxylic acid substituted for a single amino acid.

255 rst catalytic intramolecular cyclizations of carboxylic acid substrates using this Lewis acid.

256 Many other CECs are also carboxylic acids, such as the profens.

257 a direct measurement of the adsorption of a carboxylic acid surfactant to the interface.

258 boxylic and amines ( section 2 ); the use of carboxylic acid surrogates ( section 3 ); and the use of

259 uction and expression of aminocyclopropane-1-carboxylic acid synthase gene, the first committed step

260 ell lines depend on glutamine as a major tri-carboxylic acid (TCA) cycle anaplerotic substrate to sup

261 At present, most FFA4 ligands are carboxylic acids that are assumed to mimic the endogenou

262 ,6,6-tetramethyl-piperidine-1-oxyl-4-amino-4-carboxylic acid, the probe is rigidly and stereospecific

263 se of electron-rich alkynes or highly acidic carboxylic acids, the reaction rate could be increased.

264 tor has been employed for the methylation of carboxylic acids, the synthesis of alpha-chloro ketones

265 (DA) is used to convert the TAT's amines to carboxylic acid; the resulting DA-TAT is conjugated to p

266 s well as a diverse range of natural-product carboxylic acids, thereby demonstrating its broad utilit

267 divergent resolution of racemic alpha-chiral carboxylic acids, thus providing access to a variety of

268 atic system by coordination of an amine or a carboxylic acid to the boron center enabled N-H activati

269 ) catalyze the reduction of a broad range of carboxylic acids to aldehydes using the cofactors adenos

270 fers and a novel route for the conversion of carboxylic acids to alkenes.

271 catalyzed coupling of alpha,beta-unsaturated carboxylic acids to aryl alkenes to access chiral alpha-

272 nd stereospecific intermolecular addition of carboxylic acids to iodoalkynes.

273 n the regioselective Markovnikov addition of carboxylic acids to terminal alkynes, yielding valuable

274 lexes that specifically respond to amines or carboxylic acids - two classes of semiochemicals that ha

275 N-hydroxyphthalimide ester derivative of the carboxylic acid under visible light at room temperature

276 ect conversion of arylacetic acids into aryl carboxylic acids under metal-free conditions has been de

277 e method is applicable to a large variety of carboxylic acids using diazo compounds that are formed f

278 carbons and the Schmidt reaction of aromatic carboxylic acids using the superacidic trimethylsilyl az

279 ns from a variety of benzoisothiazolones and carboxylic acids using triethylphosphite as the terminal

280 step-economic alpha,beta-dehydrogenation of carboxylic acids via enediolates is reported through the

281 The average indoor concentration of carboxylic acids was 6.8 ppb, of which 87% was contribut

282 A series of nine polyfluorinated carboxylic acids was discovered, each differing by CF2CH

283 of this direct amination protocol, aromatic carboxylic acids were additionally chosen as substrates.

284 ighest number of carbohydrates, polymers and carboxylic acids were consumed in the SF sourdough.

285 Both aromatic and aliphatic carboxylic acids were converted to the corresponding thi

286 A wide variety of carboxylic acids were identified indoors and outdoors, i

287 compounds were transformed to perfluorinated carboxylic acids, which underwent further degradation un

288 xidation of aldehydes to their corresponding carboxylic acid while reducing NAD(P)(+) to NAD(P)H via

289 four metal-binding sites in the form of four carboxylic acids, while zirconyl chloride octahydrate is

290 The replacement of a carboxylic acid with a surrogate structure, or (bio)-iso

291 captodative radical by replacing the vinylic carboxylic acid with an amide.

292 al light-induced decarboxylative coupling of carboxylic acids with (hetero)aromatic nitriles at ambie

293 e reaction of either coumarins or coumarin-3-carboxylic acids with aromatic aldehydes.

294 that enables chemists to couple simple alkyl carboxylic acids with aryl zinc reagents under Ni-cataly

295 ng of primary, secondary, and tertiary alkyl carboxylic acids with both aryl and heteroaryl organomet

296 zed decarboxylative coupling of heterocyclic carboxylic acids with heterocyclic halides to achieve th

297 ecades to make simple C-N (amide) bonds from carboxylic acids with loss of water can be used to make

298 Formation of carboxylic acids with molecular weight (MW) 216 Da (most

299 ters (both isolated and derived in situ from carboxylic acids) with organozinc and organomagnesium sp

300 rovided good yields of nitrile products from carboxylic acids, with complete retention of isotopic pu