ライフサイエンスコーパス: catechol

1 2.57 DeltaA420nm/minx10(-1), determined with catechol.

2 intermediates including protocatechuate and catechol.

3 y for chlorogenic acid, 4-methylcatechol and catechol.

4 ounds gave better activities than trolox and catechol.

5 diCl, and 2,4,6-triCl-phenol), and 3,5-di-Cl-catechol.

6 ging from 18% for phenol to 46% for 3,5-diCl-catechol.

7 I), with a stronger effect for guaiacol than catechol.

8 om coniferyl alcohol-derived lignin, to form catechol.

9 conducting glass substrate for detection of catechol.

10 that deliver either meta- or para-methylated catechols.

11 etabolize additional host- and plant-derived catechols.

12 surface-functionalized with mussel-inspired catechols.

13 pon enzymatic oxidation, result in connected catechols.

14 we produced adipic acid from catechol using catechol 1,2-dioxygenase (CatA) and a muconic acid reduc

15 .0 ppmv O3(g) with microdroplets containing [catechol] = 1-150 muM.

16 4-(Pentafluorosulfanyl)catechol, 2-amino-4-(pentafluorosulfanyl)phenol, and 2-a

17 Optimal temperatures were 40 degrees C for catechol, 25 degrees C for 4-methylcatechol and 20 degre

18 lution containing gallic acid (GA), 4-methyl-catechol (4-MC), in which the concentration of the pheno

19 SimCells were used to synthesize catechol (a potent anticancer drug) from salicylic acid

20 This work shows how catechol, a molecular probe of the oxygenated aromatic h

21 A biomimetic adhesive polymer, poly(catechol-acrylic acid), was examined in conjunction with

22 tial progress with the identification of non-catechol agonists with suitable properties to progress t

23 nt synthesis of benzoxazole derivatives from catechols, ammonium acetate as the nitrogen source, and

24 control unit for the detection of oxygen and catechol analytes, which are central to medical and envi

25 Dioxygenation of nitrobenzene to catechol and 2-nitrotoluene to 3-methylcatechol showed l

26 The optimal pH values were 5.5 for catechol and 4-methylcatechol and 5.0 for chlorogenic ac

27 n electrophoretic separation of dopamine and catechol and a micellar electrokinetic chromatography se

28 against a monomer architecture in which the catechol and amine were coupled together in a fixed orie

29 3-dihydroxybenzoylglycine (H3L), which bears catechol and carboxyl functionalities in tandem, on to t

30 Mussel-inspired adhesives containing paired catechol and cationic functionalities are a promising cl

31 ates that direct intramolecular adjacency of catechol and cationic functionalities is not necessary f

32 variations in intramolecular spacing between catechol and cationic functionalities.

33 eview describes the crosslinking pathways of catechol and derivatives in both natural and synthetic s

34 of PiuA Fe(III)-bis-catechol and Ga(III)-bis-catechol and Ga(III)-(NE)(2) complexes by NMR spectrosco

35 Structural analysis of PiuA Fe(III)-bis-catechol and Ga(III)-bis-catechol and Ga(III)-(NE)(2) co

36 The reactions of Fe(III) with catechol and guaiacol produced significant changes in th

37 mechanism were shown to include oxidation of catechol and guaiacol to hydroxy- and methoxy-quinones.

38 Here, dark reaction of Fe(III) with catechol and guaiacol was investigated in an aqueous sol

39 and benzoic acids as well as phenols such as catechol and its derivatives from the action of colonic

40 s-bacterial iron chelators-consist of paired catechol and lysine functionalities, thereby providing a

41 Catechol and phenol, which were persistent biotransforma

42 products that did not transform further were catechol and phenol.

43 promoted oxidation-induced cross-linking of catechol and subsequently decreased its adhesive propert

44 rtant 0.1-1 muM range and in the presence of catechol and such dopamine precursors and metabolites as

45 the electron density on the oxygen atoms of catechol and, in turn, the propensity of the catechol to

46 Coupling of catechols and amines in the same monomer side chain prod

47 Recently, catechols and amines-two functionalities that account fo

48 secrete proteins rich in residues containing catechols and cationic amines that displace hydration la

49 or para quinones to obtain the corresponding catechols and hydroquinones in good to excellent yields.

50 Catechols and inflammatory marker levels were measured i

51 lating functional groups (i.e., hydroxamate, catechol, and mixed type).

52 side (vitisin B), pyranomalvidin-3-glucoside-catechol, and pyranomalvidin-3-glucoside-epicatechin] us

53 logical diols such as fructose, glucose, and catechol, and the thiosemicarbazide-functionalized nopol

54 at incorporated carboxylic acid side chains, catechols, and sequences derived from phage display sele

55 ored complexes by the known reaction between catechol- and pyrogallol-containing anthocyanins and alu

56 ors describing the concentration of adsorbed catechol are very similar suggesting that light does not

57 from Agaricus bisporus (abTYR), phenols and catechols are oxidized to highly reactive o-quinone inte

58 f the 5-Cl substitution of compound 1 on the catechol aryl ring system led to a new analogue compound

59 able sensor platform and electrocatalyst for catechol as probe in aptasensor.

60 ydrogen peroxide as the enzyme substrate and catechol as redox mediator was employed to monitor the a

61 e inactivation in between 2.0</=pH>10, using catechol as substrate.

62 tested for phenolic compound detection, with catechol as target analyte, in the linear range 2.5-50 m

63 , resulting in a facile one-pot synthesis of catechols, as well as the incorporation of a variety of

64 arboxyethyl)phosphinate functionality with a catechol-based fragment, which are designed for complexa

65 Clinical development of catechol-based orthosteric agonists of the dopamine D1 r

66 greater control over properties of synthetic catechol-based polymers and adhesives.

67 dences demonstrated that the coordination of catechols bearing EDGs led to deep-red positively charge

68 These catechol-bearing dendrons provide a fast and efficient m

69 d cations from the mineral surface, allowing catechol binding to underlying oxides.

70 The catechol biosensor exhibited wide sensing linear range f

71 lytical performances were investigated for a catechol biosensor, based on the PEDOT-rGO-Fe2O3-PPO com

72 Most notably, 1 reacts with catechol borane to afford the unprecedented hydroborylen

73 reactions between ortho-difluoro benzene and catechol building units, which form ether linkages.

74 ruction to the electrocatalytic oxidation of catechol by Ag@Pt-GRs after binding to the surface of el

75 mation via the one-electron oxidation of the catechol by approximately 400 mV (9 kcal mol(-1)).

76 nitroaromatic compounds to the corresponding catechols by two enzymes, namely, nitrobenzene and 2-nit

77 In more detail, we chose catechols carrying either an electron-donating group (ED

78 interaction between boronic acids (BAs) and catechols (CAs) into synthetic nucleobase analogs.

79 However, we show that increasing the catechol-cation spacing by incorporating nonbinding doma

80 in a molecule reduces adhesion, and (3) the catechol-cation synergy is greatest when both functional

81 A mechanism for catechol-cation synergy is proposed based on electrostat

82 er via a cooperative binding effect known as catechol-cation synergy.

83 brication of laccase biosensor to detect the catechol (CC) using laccase immobilized on graphene-cell

84 for further investigation of the complicated catechol chemistry.

85 Aniline-modified DNA was coupled to catechol-coated electrodes that were oxidized to o-quino

86 The Mo-catechol complex (2a) was found to react within minutes

87 By binding to ferric catechol complexes, SCN can sequester iron, a growth-lim

88 inear variation of amperometric current with catechol concentration.

89 In this work, a polymer-catechol conjugate containing a superhydrophilic nonfoul

90 The corresponding bis-catechol conjugate, 42, has excellent activity against G

91 Marine mussels secret catechol-containing adhesive proteins that enable these

92 ation to deactivate the adhesive property of catechol-containing adhesive that is in direct contact w

93 hanging the reaction time and the underlying catechol content, the final DNA surface coverage could b

94 y incorporating sacrificial, reversible iron-catechol cross-links into a dry, loosely cross-linked ep

95 The novel boronate-catechol crosslinked nanocarrier platform demonstrated i

96 e oligonucleotide generated by two oxidants, catechol/Cu(2+)/NADPH and Fenton's reagent, were located

97 45, and 248 were most frequently oxidized by catechol/Cu(2+)/NADPH with relative oxidation of 5.6, 7.

98 However, under an O2 environment, catechol degradation decreased when SCT was <1 mug/mg bu

99 matite coating on a silica surface inhibited catechol degradation in N2, especially at low catechol l

100 The introduction of O2 into the catechol degradation system substantially decreased the

101 Finally, we observe catechol dehydroxylation in the gut microbiotas of diver

102 Catechol dehydroxylation is a central chemical transform

103 is of hinduchelins A-D, a family of nontoxic catechol derivatives from Streptoalloteichus hindustanus

104 cluding several hydroquinone, resorcinol and catechol derivatives, either chlorinated or not.

105 nitial attempts to identify agonists yielded catechol derivatives, mimicking dopamine, with suboptima

106 e phenols, such as p-hydroxybenzoic acid and catechol, derived from the catabolism of gallotannins, e

107 Importantly, we demonstrate that catechol-derived oxidants can be quantified in human neu

108 tivity of Ag@Pt-GRs towards the oxidation of catechol, determination of TNF-alpha antigen was based o

109 Earlier analogues of the catechol diether compound series have picomolar activity

110 binding modes and future optimization of the catechol diether series.

111 series of very potent nanomolar to picomolar catechol diethers.

112 ds I and II, which are members of a class of catechol diethers.

113 ere separated and identified by LC-ESI-MS as catechol-diglycine adduct that undergoes polymerization

114 nolic compounds in E. polonica, initiated by catechol dioxygenase action, are important to the infect

115 s were identified in E. polonica that encode catechol dioxygenases carrying out these reactions.

116 criminates nine diol-containing bioanalytes--catechol, dopamine, fructose, glucose, glucose-1-phospha

117 n the enzyme-catalyzed para-carboxylation of catechols, employing 3,4-dihydroxybenzoic acid decarboxy

118 ridium-catalysed tyrosinase-like approach to catechols, employing an oxyacetamide-directed C-H hydrox

119 that gamma-terpinene can reduce quinones to catechols enabling their antioxidant activity.

120 In situ generation of boronic acid catechol ester derivatives generates RH(2)C(*) radicals

121 fections, including roles for metabolites of catechol estrogen and oxysterols of parasite origin as i

122 ese helminth infections, including roles for catechol estrogen- and oxysterol-metabolites of parasite

123 s to target optimal conditions for detecting catechol estrogens (CEs)-adducted human serum albumin (H

124 Catechol estrogens also generated sustained elevations i

125 In insulin-secreting cells, catechol estrogens produced rapid activation of calcium

126 We show that catechol estrogens, hydroxylated at positions C2 and C4

127 fects of major natural estrogen metabolites, catechol estrogens, on insulin secretion in pancreatic b

128 ting insulin secretion than any other tested catechol estrogens.

129 Fe-hemin binding protein, binds tetradentate catechol Fe(III) complexes, including NE and the hydroly

130 Uptake and photoreactivity of catechol-Fe complexes are investigated at the gas/solid

131 enhances the initial photodecay kinetics of catechol-Fe complexes at 30% RH by a factor of 10 relati

132 lts on dark iron-catalyzed polymerization of catechol forming insoluble black polycatechol particles

133 om 3.5 to 7.5) and substrate concentrations (catechol from 0 to 0.5M).

134 antABC encoding enzymes for the synthesis of catechol from anthranilate, a precursor of the PQS, were

135 d amino acid dopa (DOPA) in mussel adhesion, catechol functional groups have become commonplace in me

136 A synthetic strategy to incorporate catechol functional groups into benzoxazine thermoset mo

137 driven adsorption and subsequent binding of catechol functionalities.

138 we attribute to a decrease in the density of catechol functionalities.

139 s study, copolyampholytes, which combine the catechol functionality with amphiphilic and ionic featur

140 to the Dopa (3,4-dihydroxyphenylalanine) or catechol functionality, which continues to raise concern

141 ssel-inspired wet adhesion typically entails catechol functionalization of polymers and/or polyelectr

142 Despite the success in developing catechol-functionalized materials, the crosslinking chem

143 by means of mussel-inspired metal-chelating catechol-functionalized polymer networks, biological sel

144 micking the natural proteins using synthetic catechol-functionalized polymers.

145 After premixing a catechol-functionalized weak polyanion with a polycation

146 A class of novel non-catechol G protein-biased agonists of the dopamine D(1)

147 activity with pyrogallol, 3-methylcatechol, catechol, gallic acid, and protocatechuic acid.

148 les enter plant cells, conjugate enediol and catechol group-rich flavonoids in situ, and exit plant c

149 Molecular dynamics simulations confirm that catechol groups anchor to a variety of mineral surfaces

150 Yet, the complex redox chemistry of catechol groups complicates cross-link regulation, hampe

151 Redox active catechol groups in melanins permit efficient and reversi

152 ated with polydopamine (PDA), whose reducing catechol groups subsequently immobilized silver ions in

153 ith molecules bearing enediol and especially catechol groups.

154 (2H(+)/2e(-)), i.e., the first 1H(+)/1e(-) (catechol--> phenoxyl radical) and the second 1H(+)/1e(-)

155 rmed from the dark aqueous phase reaction of catechol, guaiacol, fumaric, and muconic acids with Fe(I

156 The role of antiradical moieties (catechol, guaiacyl and carboxyl group) and molecular con

157 Ligands composed of a catechol head group and an antagonist-like oxypropylene

158 al nature of their iron-chelating group (ie, catechol, hydroxamate, alpha-hydroxyl-carboxylate, or mi

159 inase-based biosensor capable of determining catechol in natural water samples with a limit of detect

160 yrosinase-containing ink were used to detect catechol in natural water samples.

161 ltammetric determination of hydroquinone and catechol in solutions of increasing complexity and appea

162 Monitoring of catechol in water using cost-effective, handheld sensor

163 ) increasing the ratio of cationic amines to catechols in a molecule reduces adhesion, and (3) the ca

164 f difluorobenzodioxoles can be prepared from catechols in two steps through conversion into thionoben

165 Biosensor response is characterized towards catechol, in terms of graphene oxide concentration, numb

166 mutants and can be used to prepare alkylated catechols, including ethyl vanillin.

167 Catechol is electrochemically detected by means of cycli

168 veloped strip attributed to the detection of catechol is observed at -0.26 V in cyclic voltammetry.

169 derstanding of the crosslinking mechanism of catechols is of vital importance.

170 zed materials, the crosslinking chemistry of catechols is still a subject of debate.

171 The atmospherically relevant nitration of catechols is taken as a case example.

172 c acid from lignin-derived monomers, such as catechol, is a greener alternative to the petrochemical-

173 reduction of silver ions in the presence of catechol, leading to the in situ deposition of silver pa

174 on, whereas PMMA:11 mum is better suited for catechol-like polyphenol analysis.

175 Using branched catechols likely found in pretreated lignin, we found th

176 atechol degradation in N2, especially at low catechol loadings on solid particles (SCT).

177 The adjacent catechol-lysine placement provides a "one-two punch," wh

178 hlorophenol, 2-chlorophenol, salicylic acid, catechol, maleic acid, oxalate, and urea), the DeltaEE o

179 as a broad substrate range; and an inducible catechol meta-cleavage pathway gene cluster adoXEGKLIJC.

180 dichlorobiphenyl-4-ol) and the corresponding catechol metabolite, 4,5-di-OH-PCB 11 (3',5-dichloro-3,4

181 icological investigation, particularly since catechol metabolites are likely reactive and toxic.

182 KEY POINTS: The catechol metabolites of 17beta-oestradiol (E2 beta), 2-h

183 ines ionoprinting techniques with reversible catechol-metal ion coordination chemistry found in musse

184 ing reactive oxygen species but also provide catechol moieties for the iron cross-linkages.

185 The consequences of decoupling amino and catechol moieties from each other were compared (that is

186 ated by hydrogen bonding between interfacial catechol moieties, and consolidated by the recruitment o

187 udes a second order in both boronic acid and catechol moieties, and inverse second order in MeOH conc

188 h the slow autoxidation and cross-linking of catechol moieties.

189 nger, partially contributed by its molecular catechol moieties.

190 Derivative synthesis identified the catechol moiety as an important design feature in the ad

191 f the phenolic group to give an intermediate catechol moiety that is subsequently O-alkylated.

192 icating 2H(+)/2e(-) processes as inherent to catechol moiety.

193 eacting different ratios of C3-symmetric DBA catechol monomers with C2-symmetric pyrene-2,7-diboronic

194 drolytic products of more stable substrates (catechol monophosphate, ascorbic 2-phosphate and hydroqu

195 e ligand 4,5-bis(pyridine-2-carboxamido)-1,2-catechol ((N,O)LH4) with Mn(III) affords the chain compo

196 echol-O-methyltransferase (COMT), regulating catechol neurotransmitter catabolism.

197 trophenol in the photo-oxidation of 4-methyl catechol not partitioning into the aerosol phase until i

198 ically the S-adenosyl-l-methionine pocket of catechol O-methyl transferase allowed the identification

199 Human catechol O-methyltransferase (COMT) has emerged as a mod

200 Catechol O-methyltransferase (COMT) inhibitors are an es

201 e its application for drug discovery using a catechol O-methyltransferase and its inhibitors entacapo

202 of the methyl-transfer reaction catalyzed by catechol O-methyltransferase and modeled by hybrid QM/MM

203 y of properties is observed between GNMT and catechol O-methyltransferase, despite significant differ

204 e modified by variation in the gene encoding catechol O-methyltransferase.

205 conclusion, redox-active ligands containing catechol, o-aminophenol or o-phenylenediamine moieties s

206 ocusses on metal complexes containing either catechol, o-aminophenol or o-phenylenediamine type ligan

207 abolomic signature of two models of disease, catechol-O-methyl transferase (COMT(-/-)) and endothelia

208 nt non-linear interaction between two genes--catechol-O-methyl transferase (COMT) and dysbindin (dys;

209 rily regulate prefrontal dopamine clearance--catechol-O-methyl transferase (COMT) and two isoforms of

210 pone and entacapone are potent inhibitors of catechol-O-methyl transferase (COMT) for the treatment o

211 Specifically, using the brain penetrant catechol-O-methyl transferase (COMT) inhibitor tolcapone

212 demonstrated that copy number elevations of catechol-O-methyl-transferase (COMT) or Tbx1, two genes

213 abolites suggest that enzymatic catalysis by catechol-O-methyl-transferase (COMT) predominates over D

214 undant expression of the DA catalytic enzyme catechol-O-methyl-transferase (COMT), but negligible exp

215 i) to determine whether polymorphisms in the catechol-O-methyltransferase (COMT) gene affect the rela

216 The catechol-O-methyltransferase (COMT) gene is located in t

217 Functional genetic variants in the catechol-O-methyltransferase (COMT) gene result in a dif

218 In particular, the catechol-O-methyltransferase (COMT) gene, located on chr

219 a functional polymorphism (Val158Met) in the catechol-O-methyltransferase (COMT) gene, whose protein

220 fficacy might be modified by variants of the catechol-O-methyltransferase (COMT) gene.

221 or placebo (n = 537) and were stratified by catechol-O-methyltransferase (COMT) genotype activity (h

222 Catechol-O-methyltransferase (COMT) modulates dopamine l

223 Additionally, catechol-O-methyltransferase (COMT) polymorphism has bee

224 our-hour urinary hydroxytyrosol and HVAL and catechol-O-methyltransferase (COMT) rs4680 genotypes wer

225 und a dramatic increase in the expression of catechol-O-methyltransferase (COMT), along with a lower

226 Catechol-O-methyltransferase (COMT), an important therap

227 he DAT1 VNTR and functional polymorphisms in catechol-O-methyltransferase (COMT), DRD2, and DRD4 were

228 Enzymatic methyl transfer, catalyzed by catechol-O-methyltransferase (COMT), is investigated usi

229 is amplified by allelic variants in a gene, catechol-O-methyltransferase (COMT), regulating catechol

230 For catechol-O-methyltransferase (COMT), the Val(158)Met pol

231 (OPRD1), cannabinoid receptor 1 (CNR1), and catechol-o-methyltransferase (COMT), was strongly associ

232 ion of a fungal tyrosinase and the mammalian catechol-O-methyltransferase (COMT), which can effect th

233 n the expression of tyrosine hydroxylase and catechol-O-methyltransferase (COMT).

234 he rs4680 single-nucleotide polymorphism for catechol-O-methyltransferase (COMT).

235 em and how our genetic profile (specifically catechol-O-methyltransferase [COMT] polymorphisms) impac

236 ently reported isotope-effect variations for catechol-O-methyltransferase and its mutant structures.

237 a novel, once-daily, potent third-generation catechol-O-methyltransferase inhibitor.

238 e-derivatives like 3-iodothyronamine (T1AM), catechol-O-methyltransferase products like 3-methoxytyra

239 a proof-of-concept, we study three enzymes (catechol-O-methyltransferase, glucose-6-phosphate dehydr

240 The cleavage of catechol occurs at the 1,2 carbon-carbon bond at the air

241 Cyclic voltammetric studies of catechol on the enzyme modified electrode revealed highe

242 Catechol, one of the major effluents released by various

243 determining the effect of AA and EDTA on the catechol or galloyl iron binding ability of pure phenoli

244 icals via double processes by involvement of catechol or guaiacyl moiety.

245 oxidase (PPO), also known as tyrosinase and catechol oxidase, is the enzyme responsible for enzymati

246 and tyramine), the enzyme is classified as a catechol oxidase.

247 Tyrosinases and catechol oxidases belong to the family of polyphenol oxi

248 suggest that the physiological role of plant catechol oxidases were previously underestimated, as the

249 and oxidation of phenolic compounds, whereas catechol oxidases were so far defined to lack the hydrox

250 diffuse reflectance spectra and tracking of catechol oxidation byproduct, hydrogen peroxide, confirm

251 oup, together with the MOM-protection in the catechol part of the tetrahydroisoquinoline ring system,

252 Catechols play an important role in many natural systems

253 i(II)) were successfully incorporated into a catechol porous organic polymer (POP) and characterized

254 ression of antABC genes, and thus, increases catechol production.

255 bioactive natural products, obolactone and a catechol pyran isolated from Plectranthus sylvestris ( L

256 This work shows how catechol, pyrogallol, 3-methylcatechol, 4-methylcatechol

257 an form over a wide range of boronic acid-to-catechol ratios, thus producing frameworks with composit

258 DA and other catechols readily oxidize into highly reactive o-quinone

259 s - functionalized with an aniline and a 1,4-catechol respectively - preferentially react with each o

260 Marine mussels use catechol-rich interfacial mussel foot proteins (mfps) as

261 ed to radiofluorinate a highly electron-rich catechol ring in the presence of an amino acid.

262 s favourably influenced by the presence of a catechol (ring-B) and enol (ring C) function.

263 gests the potential utility of antimicrobial catechol siderophore mimetics in managing bacterial infe

264 es increases, while under Mo-limitation only catechol siderophore production is increased, with the s

265 A competitive monofunctional catechol slows COF-5 formation but does not redissolve a

266 rmance is demonstrated by testing 0.1-12 ppm catechol solutions.

267 te Fe(III) complexes formed by mono- and bis-catechol species are important Fe sources in Gram-positi

268 Compounds lacking the catechol structure had a decreasing order of H-atom and

269 The catechol structure improved both hydrogen and electron d

270 s capable of directly carboxylating aromatic catechol substrates under ambient conditions.

271 ylation of tetrahydroisoquinoline (THIQ) and catechol substrates.

272 Exploiting the amino-catechol synergy, polymeric pressure-sensitive adhesives

273 a series of physiologic unconjugated urinary catechols that were able to function as SCN ligands of w

274 atalyses the aerobic oxidation of phenols to catechols through the binuclear copper centres.

275 Borinic acids reversibly bind catechol to form boron "ate" complexes (BACs) that alter

276 tion reactions between arylboronic acids and catechol to give boronate esters are the most favored th

277 h from the condensation of boronic acids and catechols to the dehydrative trimerization of polyboroni

278 catechol and, in turn, the propensity of the catechol toward electrochemical oxidation.

279 and epicatechin-3-gallate (ECG)) and not the catechol-type catechins (catechin and epicatechin).

280 ation to form phenols and polyphenols (e.g., catechol) typically identified in the complex mixture of

281 rategy to control the oxidation potential of catechol using borinic acids is presented.

282 Here, we produced adipic acid from catechol using catechol 1,2-dioxygenase (CatA) and a muc

283 rovides a convenient route to (18)O-labelled catechols using (18)O-labelled acetic acid.

284 does not significantly enhance the uptake of catechol vapor on FeCl3.

285 ghly boronic acid-deficient to networks with catechol voids.

286 as of 1.74mM; for pyranomalvidin-3-glucoside-catechol was 1.17mM and for pyranomalvidin-3-glucoside-e

287 Determination of catechol was carried out successfully by Differential Pu

288 Catechol was chosen as a simple model for organics in ae

289 byproduct, hydrogen peroxide, confirmed that catechol was oxidized as a result of applied electricity

290 Catechol was the most readily oxidized substrate followe

291 g fermentation while dihydrocaffeic acid and catechol were produced.

292 Functionalized acyl-substituted phenols and catechols were obtained in 29-97% yields with high chemo

293 , protocatechuic acid, 4-methylcatechol, and catechol) were computationally studied using density fun

294 ounds, methyl chavicol, toluene and 4-methyl catechol, were investigated at the European Photoreactor

295 amine, carboxylic acid, thiol, aldehyde, and catechol, were prepared and chemically characterized.

296 nts demonstrated the highest affinity toward catechol, whereas PPO from BABA-elicited lettuce showed

297 ed at different rates, with the exception of catechol, which resulted in irreversible inhibition.

298 nspired themes for wet adhesion by combining catechol with hydrophobic and electrostatic functional g

299 The oxidative coupling of o-aminophenols or catechols with aniline functional groups is chemoselecti

300 chieves one-step, redox-neutral synthesis of catechols with diverse substituent groups under mild con

301 lied to the synthesis of different important catechols with fluorescent property and bioactivity from