ライフサイエンスコーパス: aromatic compound

1 ives constituting a natural family of "novel aromatic compounds".

2 ed to strongly Raman active ligands (such as aromatic compounds).

3 acids and an unidentified orto-disubstituted aromatic compound.

4 r depicting the bonding of large macrocyclic aromatic compounds.

5 410nm and 625nm among the other tested nitro-aromatic compounds.

6 ch are common modes of action for polycyclic aromatic compounds.

7 this amino acid is precursor of phenolic and aromatic compounds.

8 tion of tropical-fruity and green-herbaceous aromatic compounds.

9 ganisms sense and chemotactically respond to aromatic compounds.

10 n their para-cycloaddition with a variety of aromatic compounds.

11 solubilized fragments of lignin into monomer aromatic compounds.

12 es of unified O, N, and C atoms of amide and aromatic compounds.

13 ntiodiscrimination capabilities toward small aromatic compounds.

14 rates and is a potential source for valuable aromatic compounds.

15 of bacteria to the anaerobic degradation of aromatic compounds.

16 counted for a small proportion of alkene and aromatic compounds.

17 in selective and sensitive identification of aromatic compounds.

18 bly one of the key aspects that characterise aromatic compounds.

19 tained in the OMVs are active and catabolize aromatic compounds.

20 ith halogenated acetic acids and halogenated aromatic compounds.

21 high-octane gasoline with minimal content of aromatic compounds.

22 , which is responsible for the metabolism of aromatic compounds.

23 m biomass can become a sustainable source of aromatic compounds.

24 nologies resulted in lower emission rates of aromatic compounds.

25 tional effect may reflect the lower HOMOs of aromatic compounds.

26 prenyltransferases that generates lipophilic aromatic compounds.

27 carboxylic acids and the least for (hetero-) aromatic compounds.

28 hat undergo C-C bond cleavage to give simple aromatic compounds.

29 n focused mainly on the separation of highly aromatic compounds.

30 alyze cis-dihydroxylation of a wide range of aromatic compounds.

31 ing an independent validation data set of 30 aromatic compounds.

32 , however, was unable to degrade most of the aromatic compounds.

33 -alkanes, but did not appreciably affect the aromatic compounds.

34 ful insight for the synthesis of substituted aromatic compounds.

35 cts from Ir-catalyzed C-H polyborylations of aromatic compounds.

36 iodination reaction of different classes of aromatic compounds.

37 istinctive varietal and fermentation-derived aromatic compounds.

38 epted that closo-boranes and -carboranes are aromatic compounds.

39 e of M. vanbaalenii PYR-1 to seven different aromatic compounds.

40 f FBDD has centered on the use of sp(2)-rich aromatic compounds.

41 which is able to interact with electron poor aromatic compounds.

42 iles or undergoes Friedel-Crafts addition to aromatic compounds.

43 y steering discovery efforts toward achiral, aromatic compounds.

44 romising catalyst for the synthesis of nitro-aromatic compounds.

45 sformation is applicable to a broad range of aromatic compounds.

46 the recovery of large amounts of carbon from aromatic compounds.

47 the reductive dehalogenation of chlorinated aromatic compounds.

48 usters encoding the degradation of different aromatic compounds.

49 cids, as well as minor amounts of amides and aromatic compounds.

50 e for synthesis of complex sulfur-containing aromatic compounds.

51 the biological conversion of lignin-derived aromatic compounds.

52 often used to treat water contaminated with aromatic compounds.

53 rbon sources, including inorganic carbon and aromatic compounds.

54 he existence of diatropic currents in planar aromatic compounds.

55 ange of high O/C aliphatic, unsaturated, and aromatic compounds.

56 ogy efforts to valorize previously underused aromatic compounds.

57 amination of nitrogenous and non-nitrogenous aromatic compounds.

58 applied for the selective detection of nitro-aromatic compounds.

59 ce, to enable the investigation of dissolved aromatic compounds.

60 th 21 different carbocyclic and heterocyclic aromatic compounds.

61 ARIA in the forward mode is evaluated for 29 aromatic compounds (100 peaks) by comparison of predicte

62 rse mode of SPARIA has been tested on the 29 aromatic compounds (100 peaks) that were used to evaluat

63 ined for five phthalates and two chlorinated aromatic compounds: 120 ppm for butyl benzyl phthalate,

64 surface SOA in the eastern U.S., followed by aromatic compounds (13.2%), sesquiterpenes (13.0%) and m

65 The pheromone consists of an aromatic compound (2-phenylundecane), cuticular hydrocar

66 reactions, including (1) HO* addition to 15 aromatic compounds; (2) addition of molecular oxygen to

67 Out of nine studied nitrogen-containing aromatic compounds, 4-cyanoaniline, N,N-dimethyl-4-cyano

68 A nonplanar polycyclic aromatic compound 6 bearing a tribenzotriquinacene (TBTQ

69 ormwater DOM is better suited to compete for aromatic-compound-adsorption sites.

70 4Cl, resulting in the isolation of different aromatic compounds after ExBox.4Cl was regenerated.

71 and some low-molecular-weight aliphatic and aromatic compounds) aggregate to form complex DOM.

72 for Cl(2) and Cl(2)O previously observed for aromatic compounds also applies to the alkenes examined.

73 It is well known that differences exist in aromatic compounds amongst grapevine varieties at ripeni

74 It was concluded that nitrogen-containing aromatic compounds and alkylbenzenes were oxidized by pe

75 ude oil due to its unique selectivity toward aromatic compounds and also due to its sensitivity.

76 ne was the processing that more affected the aromatic compounds and atmospheric cold plasma processin

77 argoes within capsules, including polycyclic aromatic compounds and complex organic drugs, to be brou

78 verted under relatively mild conditions into aromatic compounds and cycloalkanes within minutes.

79 ate conversions as well as detoxification of aromatic compounds and drugs.

80 atter consists of a mixture of aliphatic and aromatic compounds and functional groups such as amides.

81 Increased contents of aromatic compounds and glycosylated precursors closely m

82 1 from Comamonas testosteroni CNB-1 binds to aromatic compounds and initiates downstream chemotactic

83 aining butanol introduced a lower content of aromatic compounds and most importantly, lead to more co

84 utant restored chemotaxis toward nine tested aromatic compounds and nine carboxylic acids.

85 Stacking interactions between aromatic compounds and nucleobases are crucial in recogn

86 catalyzing the oxidation of aldehyde and aza-aromatic compounds and the hydrolysis of amides, moietie

87 c resonance (NMR) spectroscopy evaluated the aromatic compounds and their degradation products in sam

88 theory resulted in a clear understanding of aromatic compounds and thus had a major impact on the de

89 The specific selectivity of REMPI (i.e., aromatic compounds) and universal ionization characteris

90 Chemotaxis was induced during growth on aromatic compounds, and an analysis of a pcaY-lacZ fusio

91 aromatic compounds, halogenated heterocyclic aromatic compounds, and halogenated alkanes.

92 for complex carbohydrates, detrital protein, aromatic compounds, and hydrogen, indicating the couplin

93 ation, secondary metabolites, degradation of aromatic compounds, and multidrug and heavy metal resist

94 lux to a variety of bioactive small-molecule aromatic compounds, and to lignin, the structural compon

95 tens of ng/L for selected small (polycyclic)aromatic compounds are accessible within minutes without

96 Feedstock aromatic compounds are compelling low-cost starting poin

97 How aromatic compounds are degraded in various anaerobic eco

98 wn to exhibit activity toward lignin-derived aromatic compounds are enriched in OMVs from early to la

99 Aromatic compounds are environmental pollutants with tox

100 Phenolic and nitro-aromatic compounds are extremely toxic components of atm

101 ub-mug/L concentrations of small (polycyclic)aromatic compounds are feasible.

102 Aromatic compounds are generally toxic for microorganism

103 hods for the direct C-H functionalization of aromatic compounds are in demand for a variety of applic

104 that chemotaxis, transport and metabolism of aromatic compounds are intimately linked in P. putida.

105 Neutral aromatic compounds are likely responsible for the CYP1A

106 ey building blocks in the chemical industry, aromatic compounds are mainly derived from the catalytic

107 ration vapor pressures of phenolic and nitro-aromatic compounds are measured using Knudsen Effusion M

108 defined mutants, we show that most of these aromatic compounds are metabolized by the benzoyl-CoA pa

109 opanoid p-coumarate and structurally related aromatic compounds are produced in large amounts by gree

110 diradicaloids based on pro-aromatic and anti-aromatic compounds are summarized and discussed with reg

111 ted dienes, unsaturated carboxylic acids and aromatic compounds are thus targeted from renewable feed

112 cis-Dihydrodiols, derived from monocyclic aromatic compounds, are valuable chiral pool intermediat

113 ,4,7-trimethylphenanthroline occurs with the aromatic compound as the limiting reagent and with high

114 ts OMV-mediated catabolism of lignin-derived aromatic compounds as an extracellular strategy for nutr

115 a facile approach to employ two-dimensional aromatic compounds as modular building blocks to generat

116 of various NPs and colloids, some containing aromatic compounds as well as various metals, including

117 s of phenol as precursors to polysubstituted aromatic compounds, as exemplified by a concise synthesi

118 on syn-1,6:8,13-Biscarbonyl[14]annulene, an aromatic compound at ambient conditions that gradually l

119 e globally relevant microbial degradation of aromatic compounds at anoxic sites, catalyze a biologica

120 raarylbut-2-yne-1,4-diols with electron-rich aromatic compounds at room temperature, under p-TsOH cat

121 tial biodegradation capacity for chlorinated aromatic compounds at the oxic/anoxic interface and illu

122 as palustris grows photoheterotrophically on aromatic compounds available in aquatic environments ric

123 A parameters for heterocyclic and oxygenated aromatic compounds based on historical chamber experimen

124 tabolite pyocyanin and the susceptibility of aromatic compounds bearing electron withdrawing substitu

125 nsights into fundamental questions about how aromatic compounds behave.

126 Total annual fugitive emission of the aromatic compounds benzene and toluene, considered air t

127 leaves the beta(R)-aryl ether bond of the di-aromatic compound beta-(2-methoxyphenoxy)-gamma-hydroxyp

128 In Escherichia coli, aromatic compound biosynthesis is the process that has s

129 tissues, including 'pollen development' and 'aromatic compound biosynthetic process'.

130 her removal of less oxidized as well as more aromatic compounds ("black carbon").

131 ovide evidence for binding of a CoA-modified aromatic compound by a MarR family member.

132 dines, which easily can be oxidized to fully aromatic compounds by air in the presence of UV light or

133 have investigated the ortho-hydroxylation of aromatic compounds by an iron complex using hybrid densi

134 We optimized the substrate spectrum for aromatic compounds by introduction of the triple mutatio

135 ortho-Hydroxylation of aromatic compounds by non-heme Fe complexes has been ext

136 ach to attach small rings to a wide range of aromatic compounds by palladium-catalyzed alpha-arylatio

137 e known biochemical production of a range of aromatic compounds by plants and the presence of benzeno

138 Emissions of aromatic compounds cause air pollution and detrimental h

139 These include, in addition to O-containing aromatic compounds, complex polyether- and ester-contain

140 occaceae, fermenting carbohydrates and plant aromatic compounds, constituted the bulk of the large-in

141 so-called hybrid pathways for degradation of aromatic compounds contain beta-oxidation-like steps.

142 ties imparted by the trifluoromethylation of aromatic compounds continue to drive the discovery of no

143 The kO3 values for aromatic compounds correlated well with the energy of a

144 Such systems readily obtained from simple aromatic compounds could open up a multitude of syntheti

145 ced state and in the presence of chlorinated aromatic compounds, CprK positively regulates expression

146 has been characterized in several extradiol aromatic compound degradation pathways.

147 ributed more transcripts for sulfur cycling, aromatic compound degradation, and the synthesis of biol

148 e genes, as well as genes for autotrophy and aromatic compound degradation.

149 ntrol transcription of a complex regulon for aromatic compound degradation.

150 tiple oxygenated functionalities, polycyclic aromatic compounds depleted of hydrogen and carrying few

151 ro growth experiments have demonstrated that aromatic compounds derived from lignin can be metabolize

152 Rhodopseudomonas palustris metabolizes aromatic compounds derived from lignin degradation produ

153 bolic versatility of this species, including aromatic compounds derived from lignin.

154 of microbial clades to metabolize chitin and aromatic compounds derived from lignin.

155 BrC) is a collection of oxidized atmospheric aromatic compounds detected worldwide with broad functio

156 these species are best described as locally aromatic compounds devoid of long-range intersubunit con

157 enerated the greatest amount of butterscotch aromatic compound diacetyl and polyhydroxyalkyl pyrazine

158 In this work we demonstrate that aromatic compounds, dissolved in the hydrocarbon phase,

159 ared and used for the efficient nitration of aromatic compounds (even aniline derivatives).

160 Ellagitannins and aromatic compounds evolution in Cabernet Sauvignon wines

161 The studied compounds include alkaloids, aromatic compounds, flavonoids, volatiles, sesquiterpeno

162 ed from plant lignin as a source of valuable aromatic compounds for biofuels and other bioproducts.

163 sent essential sources of high value natural aromatic compounds for human health and industry.

164 g and biosensing, a high loading capacity of aromatic compounds for small-molecule drug delivery, and

165 applicable for the production of interesting aromatic compounds from lignin.

166 Adsorption data for 29 aromatic compounds from literature (i.e., the training d

167 most reliable approaches to assemble complex aromatic compounds from preoxidized starting materials.

168 Bacterial catabolism of aromatic compounds from various sources including phenyl

169 an efficient approach to dispose halogenated aromatic compounds (HACs).

170 ructures, including nitrated and halogenated aromatic compounds, halogenated heterocyclic aromatic co

171 c and aerobic pathways for the catabolism of aromatic compounds has never been shown before, and it m

172 Bronsted acidic sites to butene and then to aromatic compounds has thus been demonstrated.

173 The prepared aromatic compounds have a relatively high boron content

174 Some of these aromatic compounds have high economic value.

175 cal and co-workers of some large polynuclear aromatic compounds having multiple phenyl substituents p

176 nal enzyme in the degradation pathway of the aromatic compound homoprotocatechuate.

177 remote methylene oxidation is obtained in 50 aromatic compounds housing medicinally relevant halogen,

178 technique to analyze the nitrogen-containing aromatic compounds in a deasphalted crude oil due to its

179 for the reliable quantification of suitable aromatic compounds in a high throughput biodegradation s

180 (CCR) control of the anaerobic catabolism of aromatic compounds in bacteria.

181 The synthesized monomer will replace similar aromatic compounds in certain applications because of it

182 d proposed catalytic sites for manganese and aromatic compounds in class II peroxidases, including re

183 for production of branched hydrocarbons and aromatic compounds in gasoline, or longer-chain, less hi

184 o cyclizations to give varied aza-polycyclic aromatic compounds in generally good yields (27-99%, 16

185 pecies undergo polarized radical addition to aromatic compounds in high yield and selectivity.

186 rbonylation lead to three distinct groups of aromatic compounds in high yields acetals, ethanol and e

187 results in the preservation of the original aromatic compounds in raw strawberries.

188 s investigated, with the aim of manipulating aromatic compounds in SB wine.

189 ia active in processing biphenyl and related aromatic compounds in soil, revealing how carbon flows t

190 higher abundances of transporters targeting aromatic compounds in the bathypelagic realm.

191 In view of the versatility and impact of aromatic compounds in the biomedical field and in materi

192 hree-component aminomethylation of activated aromatic compounds including naphtols, phenols, pyridine

193 ction of the oxindole moiety onto a range of aromatic compounds including phenols.

194 composition and the levels of several other aromatic compounds, including anthocyanins and flavonoid

195 We find that oxygenated aromatic compounds, including phenols and methoxyphenols

196 Both polar and apolar aromatic compounds, including pyridine, benzene, p-xylen

197 e intermediates or utilized to make numerous aromatic compounds, including the Pseudomonas quinolone

198 mes for anaerobic oxidation of aliphatic and aromatic compounds, including those of candidate phyla A

199 In maize, the release of the aromatic compound indole is herbivore-specific and occur

200 id dearomative difunctionalization of simple aromatic compounds into functional small molecules amena

201 atic rings, bacteria are able to degrade the aromatic compounds into simple metabolites and use them

202 Direct C-H functionalization of aromatic compounds is a powerful tool for organic synthe

203 Direct C-H functionalization of aromatic compounds is a useful synthetic strategy that h

204 Microbial conversion of aromatic compounds is an emerging and promising strategy

205 more precisely delineated, the category of "aromatic compounds" is being more and more expanded.

206 are deficient in ferulic and coumaric acid, aromatic compounds known to be attached to arabinosyl re

207 Pressure-induced polymerization of aromatic compounds leads to novel materials containing s

208 ese nitrogen and carboxyl functionalities of aromatic compounds may also impart significant Pu chelat

209 The presence of aromatic compound metabolic pathways suggests this micro

210 e two communities hosting diverse syntrophic aromatic compound metabolizers (Syntrophus, Syntrophorha

211 n formed during the photo-oxidation of three aromatic compounds, methyl chavicol, toluene and 4-methy

212 In aromatic compounds, molecular stability originates from

213 y exploited for selective detection of nitro aromatic compounds (NACs).

214 In the series of all-carbon aromatic compounds, no example of a benzene tetraanion,

215 omatic hydrocarbons (PAHs), and heterocyclic aromatic compounds (NSO-PACs) in considerably varying am

216 However, many halogenated oligocyclic aromatic compounds occur in nature as either naturally p

217 etermine whether the differences between the aromatic compounds of both species are sufficiently sign

218 hodology in the synthesis of polysubstituted aromatic compounds of natural product and bioactive mole

219 Prediction models for kO3 were developed for aromatic compounds, olefins, and amines by quantum chemi

220 prioritized a range of structurally diverse aromatic compounds on the basis of their assigned relati

221 To assess the importance of pathways for aromatic compound oxidation that do not result in ring h

222 frequency of utilization of sucrose and the aromatic compound p-hydroxyphenylacetic acid.

223 The air monitoring of polycyclic aromatic compounds (PACs) and PAC transformation product

224 Polycyclic aromatic compounds (PACs) can have multiple sources in t

225 ealed increased concentrations of polycyclic aromatic compounds (PACs) in passive sampling devices de

226 the past 150-yr records of BC and polycyclic aromatic compounds (PACs) in sediments from two represen

227 passive air monitoring study for polycyclic aromatic compounds (PACs) in the Athabasca oil sands reg

228 to describe atmospheric uptake of polycyclic aromatic compounds (PACs) into trees.

229 tudy the sorption and mobility of polycyclic aromatic compounds (PACs) to DOC and particulate organic

230 ) products are an urban source of polycyclic aromatic compounds (PACs) to the environment.

231 Polycyclic aromatic compounds (PACs) were characterized, and xDP, x

232 configurationally stable twisted polycyclic aromatic compounds (PACs) were pursued.

233 (Enchytraeus crypticus) of native polycyclic aromatic compounds (PACs) were quantified.

234 =C(16)) and branched alkanes, and polycyclic aromatic compounds (PACs), respectively.

235 Coals contain native polycyclic aromatic compounds (PACs), which include polycyclic arom

236 e polluted by complex mixtures of polycyclic aromatic compounds (PACs).

237 cted from exposure to oil-derived polycyclic aromatic compounds (PACs).

238 riedel-Crafts adducts are also achieved with aromatic compounds (phenol, anisole, indole, and aniline

239 ion of this suite of aromatics into selected aromatic compounds potentially recoverable as an additio

240 The biodegradation of six targeted aromatic compounds present in petrodiesel was also influ

241 s and diversity with regard to the number of aromatic compounds present, clearly differing from those

242 such undesired pathways to result in diverse aromatic compounds previously not systematically targete

243 d interactions of alkyl ureas with amide and aromatic compounds, relative to interactions with water.

244 biosynthesis or microbial biodegradation of aromatic compounds, respectively.

245 y to oxidize Mn(2+) and high redox potential aromatic compounds, respectively.

246 , fresh elemental carbon, organonitrogen and aromatic compounds), secondary aerosol locally produced

247 sed levels of compounds of microbial origin (aromatic compounds, secondary or sulfated bile acids, an

248 For example, 24-DNP and other nitro-aromatic compounds should readily photodegrade in organi

249 the prototype nitrogen-containing polycyclic aromatic compounds: (substituted) 1- and 2-azanaphthalen

250 rements also indicate an apparent absence of aromatic compounds such as benzene, a lack of sulfur-bea

251 fferent properties that are usually found in aromatic compounds such as bond length equalisation, ene

252 lactones of high molecular weight, and other aromatic compounds such as some esters derived from cinn

253 ucts that include pharmaceutically important aromatic compounds such as the antibiotic tetracycline a

254 Aromatic compounds, such as 4-hydroxybenzoic acid and ph

255 assays, leading to the identification of an aromatic compound that is processed in the plant into tw

256 esent at lower concentrations are a suite of aromatic compounds that can inhibit fermentation by biof

257 ion strategy allows the conversion of simple aromatic compounds that contain ynone substituents, incl

258 y expressed for the anaerobic degradation of aromatic compounds that generate 3-methylbenzoyl-CoA as

259 WhiE and TcmN ARO/CYCs bound with polycyclic aromatic compounds that mimic the respective ARO/CYC pro

260 Sunlight depleted the pool of aromatic compounds that supported microbial growth in th

261 on of filter extracts identified eight nitro-aromatic compounds that were correlated with Abs365.

262 ntatives of a new class of chiral polycyclic aromatic compounds, the "hairpin furans".

263 constitute a new class of chiral polycyclic aromatic compounds, the "hairpin furans".

264 rous routes available for the preparation of aromatic compounds, there remain few methods that allow

265 For aromatic compounds these torsion angles are close to 0 d

266 s have been generally presumed to metabolize aromatic compounds to acetate, CO2 , H2 and formate, com

267 neration of nitrogen dioxide as a radical on aromatic compounds to give nitroarenes has been studied.

268 modulate the intracellular concentration of aromatic compounds to optimize the excretion of such pro

269 , the Rh(III)-catalyzed C-H bond addition of aromatic compounds to the N-perfluorobutanesulfinyl imin

270 he reactivity of these previously unknown BN-aromatic compounds toward organolithium compounds and br

271 can carry out C-H activation on a variety of aromatic compounds traditionally used in Pd/Ag-mediated

272 The facile iodination of aromatic compounds under mild conditions is a great chal

273 ation reactions of vinyldiazo compounds with aromatic compounds using a metal-free strategy are descr

274 atic acids with the corresponding alkenes or aromatic compounds using a prenylated flavin mononucleot

275 applied to the electrochemical detection of aromatic compounds using EIS.

276 poration of (18)F into highly functionalized aromatic compounds using sulfonium salts as leaving grou

277 crobial-mediated strategy for removing these aromatic compounds, using the purple nonsulfur bacterium

278 and are synthesized by the acylation of the aromatic compound vanillylamine (derived from the phenyl

279 The bicyclic aromatic compound was observed in a complex with La.

280 action, in which rapid primary adsorption of aromatic compounds was followed by secondary lignin-like

281 The mode of binding between the nsDNA and aromatic compounds was investigated using EIS, indicatin

282 "Foxy" aromatic compounds were also quantified by gas-chromatog

283 The detections limits for polycyclic aromatic compounds were between 0.042 and 0.25 microg/L.

284 e B0 and B20 treatments, all of the targeted aromatic compounds were degraded to below detection limi

285 e, applied voltage) on the analysis of model aromatic compounds were investigated and discussed.

286 hese proteins in complex with four different aromatic compounds were obtained.

287 Only the aromatic compounds were partitioned according to Raoult'

288 Amplification mutants that consume aromatic compounds were selected under conditions requir

289 ntrast to degradation pathways of monocyclic aromatic compounds where ring-cleavage is achieved via h

290 xidizing Betaproteobacteria and degraders of aromatic compounds, which hence impact the aquifer redox

291 sed are principally comprised of sp(2) -rich aromatic compounds, which limits the structural (and hen

292 This process generates functionalized aromatic compounds with complete regiocontrol.

293 majority of dyes industrially used today are aromatic compounds with complex, reinforced structures,

294 was selective toward degradation of various aromatic compounds with different substituents, probably

295 ombusted at 250 degrees C contains condensed aromatic compounds with low H/C and O/C ratios while ret

296 ng the highest affinity for the surface were aromatic compounds with multiple oxygenated functionalit

297 confinement in nanopores, pi interactions of aromatic compounds with polyaromatic surfaces, and very

298 served, while amino acids, organic acids and aromatic compounds with potential antioxidant activity i

299 Single-ring aromatic compounds with unsaturated C4 and C5 substituen

300 N)(6), a well-known strong electron acceptor aromatic compound, with mono- or polyatomic anions switc