ライフサイエンスコーパス: carboxylic

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

16 )-1-methyl-4-nitro-3,5-diphenylpyrrolidine-2-carboxylic acid (endo-6) and (2S,3S,4R,5S)-1-methyl-4-ni

17 )-1-methyl-4-nitro-3,5-diphenylpyrrolidine-2-carboxylic acid (exo-6), combined with 1,8-diazabicyclo[

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

54 nient precursor to access various conjugated carboxylic acid derivatives.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

76 Carboxylic acid incorporation into parent MWO hydrocarbo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

97 Carboxylic acid reductases (CARs) catalyze the reduction

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

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

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

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

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

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

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

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

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

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

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

109 (2-(2-carboxyethyl)-4-methyl-5-propylfuran-3-carboxylic acid) is a metabolite that circulates at high

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

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

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

113 4,5-dihydroxy-2,3,4,5-tetrahydropyridazine-3-carboxylic acid, a gamma-halogenated piperazic acid, and

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

129 ,6,6-tetramethyl-piperidine-1-oxyl-4-amino-4-carboxylic acid, the probe is rigidly and stereospecific

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

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

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

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

134 and the ethylene precursor aminocyclopropane-carboxylic acid.

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

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

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

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

139 electronically different substituents on the carboxylic acid.

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

141 ,2R)-/(1S,2S)-2-(carboxymethyl)cyclohexane-1-carboxylic acid] has previously been identified as metab

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

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

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

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

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

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

148 For carboxylic acids a sharp increase in sensitivity is like

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

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

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

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

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

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

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

156 (1a-e) were derived from their corresponding carboxylic acids and bidentate directing groups.

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

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

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

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

161 Higher alcohols, carboxylic acids and ketones gradually increased during

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

163 Aliphatic carboxylic acids and sulfonamides could not be different

164 Both aliphatic carboxylic acids and sulfonamides yield several fragment

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

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

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

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

169 Carboxylic acids are present in many foods, being especi

170 Alkyl carboxylic acids are ubiquitous in all facets of chemica

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

186 Selected carboxylic acids could be converted to their correspondi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

201 y fluorodecarboxylation of the corresponding carboxylic acids is reported.

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

203 While carboxylic acids measured outdoors displayed a single da

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

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

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

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

208 Alcohols and carboxylic acids preferentially captured thiiranium ions

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

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

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

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

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

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

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

216 nd stereospecific intermolecular addition of carboxylic acids to iodoalkynes.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

256 t oxidation of aldehydes to their respective carboxylic acids.

257 riegated building blocks of chemistry: alkyl carboxylic acids.

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

259 ge in regioselectivity and form unconjugated carboxylic acids.

260 from those observed for sulfones or aromatic carboxylic acids.

261 derivatives are better protective groups for carboxylic acids.

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

263 vated Ascaris eggs through exposure to these carboxylic acids.

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

265 y important derivatives such as nitriles and carboxylic acids.

266 thiol-ene modification to introduce pendant carboxylic acids.

267 ickel complex that couples aryl halides with carboxylic acids.

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

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

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

271 rated by synthesizing several derivatives of carboxylic acids.

272 before their fermentation into alcohols and carboxylic acids.

273 decarboxylation of redox-activated aromatic carboxylic acids.

274 r compared to those of the corresponding bis(carboxylic amide) derivative.

275 Because of the presence of a carboxylic amide, which has a preference for a trans-con

276 a filter favoring the release into water of carboxylic and fulvic acid-like components.

277 a sour GRN that is specifically activated by carboxylic and mineral acids but does not respond to swe

278 ionality of biochar with the introduction of carboxylic and phenolic groups, a reduction of oxonium g

279 C over the nanoparticles functionalized with carboxylic and vinyl groups.

280 electrochemical method for the synthesis of carboxylic as well as hindered esters from N-alkoxyamide

281 promoted stabilization of aliphatic C-H and carboxylic C=O compounds associated with mineral phases.

282 process with the aryl azides and alpha-diazo carboxylic esters serving as precursors for nitrogen and

283 In this study, the carboxylic functional group and an unexpected sulfonate

284 ecially by the fatty acid content (number of carboxylic functions) and the fatty acid length.

285 showed no such behavior, thus the additional carboxylic group should be responsible for the observed

286 When MB bears an additional carboxylic group, the negative charge provided by this g

287 Depending on the applied potential, ether or carboxylic groups are formed.

288 ich recognized interaction of phosphonic and carboxylic groups as decisive in phosphonocarboxylate lo

289 rbomethoxy groups were deprotected to obtain carboxylic groups used to immobilise antibodies for card

290 After activation of carboxylic groups, BSA was immobilized onto the CMD chip

291 ernal water molecules and/or ionic E194/E204 carboxylic groups.

292 ocomposite AuNPs-PANABA-MWCNTs employing the carboxylic moieties as anchor sites.

293 mine molecules appended with crown-ethers or carboxylic moieties form self-assembled supramolecular c

294 where embedding the amide group between two carboxylic moieties in proper geometries, at distances l

295 Then, the terminal carboxylic moieties on the electrodes surfaces were util

296 nt on the molecular functionality (i.e., the carboxylic or OH functional group in organic acids and m

297 On the other hand, ester groups at the carboxylic position favor ring opening, whereas amides a

298 y nature, such as dissolved black carbon and carboxylic-rich alicyclic molecules, was also rapidly an

299 onalized alkyl boronate esters from abundant carboxylic substituents.

300 timal relation of pyrrole and pyrrole-3-acid carboxylic to perform the cTnT biomimetic nanosurface wa