ライフサイエンスコーパス: aromatics

1 g indoles, anilines, and other electron-rich aromatics.

2 this strategy in the preparation of (hetero)aromatics.

3 for larger 2D N-substituted polyheterocyclic aromatics.

4 rable sites for reaction pathways leading to aromatics.

5 a multitude of commercially used halogenated aromatics.

6 with higher octane rating, 91, contained 35% aromatics.

7 and tertiary boronic esters to electron-rich aromatics.

8 als, ethanol and ethyl aromatics, and methyl aromatics.

9 bons and higher molecular weight substituted aromatics.

10 troublesome with methylenedioxy substituent aromatics.

11 e contributions of some of the alpha-subunit aromatics.

12 CalNex, about 5 times that from single-ring aromatics.

13 he biotic and abiotic hydrodehalogenation of aromatics.

14 edicted to be preferred for most fluorinated aromatics.

15 ortho borylations for a range of substituted aromatics.

16 more than 60wt% yield of low-molecular-mass aromatics.

17 y and completely degraded DOSS, alkanes, and aromatics.

18 w the specificity of preferring alkenes over aromatics.

19 cyclohexene and related cyclic olefins into aromatics.

20 st time, and provide insight into the PIP of aromatics.

21 O, allowing the halogenations of deactivated aromatics.

22 ains less lignin and less nitrogen bonded to aromatics.

23 molecular nanostructures of hexasubstituted aromatics.

24 actions between the nitronium ion and the pi-aromatics.

25 of functionalized pyrazoles, indazoles, and aromatics.

26 rganic frameworks (COFs) containing extended aromatics.

27 water retention even around the hydrophobic aromatics.

28 ndensation step to selectively produce azoxy-aromatics.

29 children and adults as hazard index > 1 for aromatics.

30 lysis, focusing mainly on other heterocyclic aromatics.

31 rapping (TMT) to a series of key fluorinated aromatics.

32 tive to other known borepin-based polycyclic aromatics.

33 f two isomeric borepin-containing polycyclic aromatics.

34 acceptors, acylating reagents, and activated aromatics.

35 and electronic structures of these nonplanar aromatics.

36 onolefinic byproducts, including alkanes and aromatics.

37 produce as much or more SOA than single-ring aromatics.

38 Three urea-based aromatics 1-3, each with distinct steric and electronic

39 of these families, i.e., o- and p-xylene as aromatics, 1-octene as an alkene, and n-octane as an alk

40 y of guests including alkanediamines (6-12), aromatics (14-32), amino acids (33-36), and nucleobases

41 , xylenes, and ethylbenzene), 40%; other VOC aromatics, 15%.

42 s of the corresponding bis(1-chloronorbornyl)aromatics 2 are also obtained from preparative-scale rea

43 A wide range of per- and polyfluorinated aromatics (21 examples), including C6F6, C6F5CF3, C6F5CN

44 5) g/h, toluene 34.43 (1.01, 126.76) g/h, C8 aromatics 37.38 (1.06, 225.34) g/h, and methane 2.3 (1.7

45 e oxidation of methylenes in the presence of aromatics(4) and N-heterocycles(5), olefins remain a lon

46 tions (DMSO, t-BuOK) with 1,2-bis(halomethyl)aromatics 6-15 to yield 4a-d and 16-24, which contain a

47 for the former and 50.0% for the latter) and aromatics (93.5% for the former and 74.2% for the latter

48 Among the aromatics, a strong bias toward Trp is clear, such that

49 s, branched alkanes, saturated cycloalkanes, aromatics, aldehydes, hopanes and steranes, and metals i

50 f UDOM contained more carbohydrates, amides, aromatics/alkenes and aliphatics, while smaller fraction

51 The method is general: alcohols, aromatics, amines, and phosphonates were all found to de

52 tribution of pure hydrocarbons (particularly aromatics and aliphatics) of the engine exhaust decrease

53 present in the reacting mixture, leading to aromatics and alkanes.

54 th previous work on the functionalization of aromatics and alkenes by Pd(II) salts.

55 hina, and the ambient VOCs were dominated by aromatics and alkenes.

56 ssociated with dehalogenation of chlorinated aromatics and appears to represent a new subtype within

57 by ProGolem detect interactions mediated by aromatics and by planar-polar residues, in addition to l

58 arger than the contribution from single-ring aromatics and comparable to that of polycyclic aromatic

59 erivatives, terpenes, alkyl ethers, ketones, aromatics and cyclic alkyl derivatives.

60 ion of carbon-based feedstocks into olefins, aromatics and gasoline.

61 o the gram scale, and a broad scope for both aromatics and halogens.

62 orobenzyl carbanions from electron-deficient aromatics and heteroaromatic rings can react with aldehy

63 Various electron-rich aromatics and heteroaromatics are useful scaffolds in th

64 and selective reduction of nitro-containing aromatics and heteroaromatics can be effected in water a

65 ction with an array of pendent electron-rich aromatics and heterocycles thus efficiently providing cy

66 d process is more effective for deborylating aromatics and is generally more effective in the monodeb

67 liphatic enol (devoid of conjugated or bulky aromatics and lacking a 1,3-diketone structural motif kn

68 rvive in sites contaminated with chlorinated aromatics and may be useful for in situ bioremediation.

69 play a role in the metabolism of halogenated aromatics and of short, medium, and long chain fatty aci

70 f Clar's analysis with respect to polycyclic aromatics and quantitatively assess the bonding and elec

71 ines, and piperidines decorated with various aromatics and substituents were thus prepared in enantio

72 s significantly increased, whereas condensed aromatics and tannins significantly decreased for the de

73 Specific systems such as the oxidation of aromatics and the current state of knowledge on OH-regen

74 The possible mechanistic roles of these aromatics and the further use of yeast genetics to disse

75 The list of heterocyclic aromatics and the mass spectral library generated in thi

76 tively sensitive nature of the electron-rich aromatics and the paucity of commercial sources pose som

77 Biodiesel use led to minor reductions in aromatics and variable changes in carbonyls.

78 group fractions (including acids, carbonyls, aromatics, and aliphatics) were calculated to characteri

79 ses of odorants: pheromones, monoterpenoids, aromatics, and aliphatics.

80 wide range of NMHCs (alkanes, cycloalkanes, aromatics, and bicyclic hydrocarbons) are released at pa

81 otable compatibility with functional groups, aromatics, and certain heteroaromatic substituents.

82 ples include long-chain alkanes, halogenated aromatics, and cyclic volatile methylsiloxanes (cVMS).

83 ehyde, dimethyl ether, heavier hydrocarbons, aromatics, and hydrogen is also reviewed.

84 er lignin is an abundant renewable source of aromatics, and its depolymerization generates a variety

85 ed from various aromatic hydrocarbons, amino aromatics, and lignin monomers, also to beta-ketoadipate

86 ds in high yields acetals, ethanol and ethyl aromatics, and methyl aromatics.

87 s of hydrocarbons, including liquid alkanes, aromatics, and oxygenates, with carbon numbers (Cn) up t

88 l (SOA) originating from isoprene, terpenes, aromatics, and sesquiterpenes.

89 es, particularly alcohols, carboxylic acids, aromatics, and sulfides.

90 able to support growth, such as methoxylated aromatics, and those that have not yet been tested, such

91 Thus, polar aromatics appear to substitute for Trp-281 to allow red

92 ral amines such as aliphatics, benzylics, or aromatics are compatible with our reaction conditions as

93 pogenic volatile organic compounds including aromatics are considered as their precursors in the atmo

94 Long, rigid guests such as p-substituted aromatics are either static or only tumble at elevated t

95 Polyfluorinated aromatics are essential to materials science as well as

96 Aromatics are formed via Diels-Alder cycloaddition with

97 The higher aromatics are found to yield carboxymethyl lactones deri

98 ressing typical catalytic reactions in which aromatics are involved, an optimal propene selectivity a

99 Halogenated aromatics are one of the largest chemical classes of env

100 A variety of substituted polycyclic aromatics are readily prepared in good to excellent yiel

101 ls and azetidinols bearing electron-donating aromatics are successful, proceeding via an azetidine ca

102 Our study suggests that, although aromatics are the minor component of polyesters, they pl

103 Brominated aromatics are used in many different applications but oc

104 carbonyls, aryl carbonyls, and electron-rich aromatics, are viable reaction partners, allowing Michae

105 c pathways for using environmentally derived aromatics as a carbon source.

106 cell assays of strain CBDB1 with brominated aromatics as electron acceptors.

107 tible with hydride, azide, and electron-rich aromatics as nucleophiles.

108 e evolved the ability to utilize chlorinated aromatics as terminal electron acceptors in an energy-ge

109 e to the D4-F2.61V mutation are sensitive to aromatics at position 2.60 (D4-L2.60W, 7-20-fold increas

110 e introduction of amines onto functionalized aromatics at specific and pre-determined positions (orth

111 The possible roles of aromatics at the end of the sixth transmembrane helix ar

112 tion of a series of borepin-based polycyclic aromatics bearing two different arene fusions.

113 xidation from the hydrosilane, electron-rich aromatics benefit from silane activation via oxidation t

114 exergonic electron transfer between neutral aromatics (benzenes and biphenyls) and their radical cat

115 zed, resulting in a decline in saturates and aromatics, but increases in resins and asphaltenes.

116 ol vinyl boronic ester and allyl-substituted aromatics by cross metathesis is reported.

117 tion of a wide range of low molecular weight aromatics by MWCNTs.

118 through the direct C-H functionalization of aromatics by the C-C coupling of halogen-free (hetero)ar

119 Although oxidation of aromatics by these radicals has been studied for decades

120 ral pathways for the anaerobic catabolism of aromatics by this strain.

121 , shedding light on the fact that monocyclic aromatics can also serve as the hitherto unrecognized pr

122 compounds (e.g., alkanes, alkenes, alkynes, aromatics, carbonyls, and polycyclic aromatic hydrocarbo

123 catalytic processes, including alkylation of aromatics, catalytic cracking, methanol-to-hydrocarbon p

124 rmed when hydroxyl- and chlorine-substituted aromatics chemisorbed on Cu(II)O and Fe(III)(2)O(3) surf

125 er temperatures, the formation of oxygenated aromatics competes with the formation of CO(2), implying

126 (v/v) to 1.18% (v/v) while keeping the total aromatics constant.

127 In particular, lignin-derived aromatics containing guaiacol and veratrole motifs were

128 olyphenols, including anthraquinones, simple aromatics containing primary or secondary alcohols, a va

129 increased by up to 60% with increasing fuel aromatics content and decreasing engine thrust.

130 , and black carbon emissions with increasing aromatics content for all seven vehicles tested.

131 The aromatics content was varied from 17.8% (v/v) in the nea

132 luding oxygen content, hydrogen content, and aromatics content.

133 Only three of the aromatics contribute significantly to DeltaGB1 at the ad

134 Alkenes and aromatics contributed to the largest fractions of photoc

135 Based on our simulation results, polycyclic aromatics could behave as natural anti-agglomerants and

136 urfactants considered here, while monocyclic aromatics could, in some cases, negatively affect perfor

137 However, structurally complex aromatics currently cannot be converted into arylamines,

138 -methoxycatechol (all proxies for oxygenated aromatics derived from benzene, toluene, and anisole) re

139 Although the signals of these heterocyclic aromatics diminished with distance, some were detected a

140 Producing aromatics directly from the smallest hydrocarbon buildin

141 , pi-conjugated, boron-containing polycyclic aromatics, DTBs are promising building blocks for the ne

142 antly higher rates and higher selectivity to aromatics, due to lower activation barriers over the sol

143 Organic molecules ranging from simple aromatics (e.g., aniline and chlorobenzene) to the much

144 se influences the regiospecific oxidation of aromatics (e.g., from o-cresol, M180H forms 3-methylcate

145 es of alkanes, alkenes, aldehydes, alcohols, aromatics, esters, and ketones with high speed and high

146 The (hetero)aromatics evaluated were divided in different categories

147 hat in some cases, fulvenes possessing fused aromatics exhibited a high degree of intermolecular pai-

148 matizing spirocyclization of alkyne-tethered aromatics far more effectively than the analogous unsupp

149 borepins (DTBs), boron-containing polycyclic aromatics featuring the fusion of borepin and thiophene

150 analysis by FID, paraffins, naphthenes, and aromatics form distinct two-dimensional separated groups

151 fuels with higher carbon numbers and/or more aromatics formed more SOA than fuels with lower carbon n

152 tential oxygenates as well as certain of the aromatics found in gasoline.

153 especially applicable to the oxygenates and aromatics found in gasolines.

154 The toxicity of aromatics frequently limits the yields of their microbia

155 Removing the aromatics from ACSH with R. palustris, allowed growth of

156 nvironment, R. palustris removes most of the aromatics from ammonia fiber expansion (AFEX) treated co

157 e the necessity of accounting for oxygenated aromatics from biomass-burning emissions and their SOA f

158 obtaining large sulfur-containing polycyclic aromatics from thienyl precursors through iron(III) chlo

159 (methanogenesis), and cat23 (oxygenation of aromatics) genes in column cores suggested more extensiv

160 l)benzotriazoles with hetero- and benzenoid- aromatics give alpha-amino ketones that can be reduced b

161 ethylated Fc, contrary to non-organometallic aromatics giving mixtures of HO and MeO derivatives.

162 all vehicle/fuel combinations with the total aromatics group being a significant contributor to the t

163 Substitution for either of these aromatics had no effect on duplex probe recognition.

164 Unlike with other oxidants such as nitro-aromatics, halocarbons do not cause additional surface r

165 g of secondary alkylzinc reagents to (hetero)aromatics has been achieved with high selectivity with P

166 er-catalyzed Finkelstein reaction of (hetero)aromatics has been developed using continuous flow to ge

167 of secondary and tertiary boronic esters to aromatics has been investigated.

168 ucidation of the role of CBM and active site aromatics has been obscured by a complex multistep mecha

169 H bond cleavage over a wide range of (hetero)aromatics has been performed in an attempt to quantify t

170 Although the nucleophilic alkylation of aromatics has recently been achieved with a variety of p

171 These aromatics have counterparts in most TRP subfamilies.

172 es of such a system, known as 'electron-rich aromatics', have been studied in detail for a long time.

173 n addition to benzoic acid, other monocyclic aromatics (i.e., benzene, toluene, salicylic acid, benzy

174 The same heterocyclic aromatics identified in snow, lake sediments, and air we

175 ed as building blocks similar to alkenes and aromatics in a petroleum refining complex.

176 e activated carbon dioxide reacting with the aromatics in a typical electrophilic substitution.

177 sified as aliphatic, aromatic, and condensed aromatics in approximately equal measure, while aliphati

178 o investigate the orientation of overcrowded aromatics in films with submonolayer coverage.

179 tend the pi-conjugation of readily available aromatics in one-dimension is of significant value.

180 The fluorescing aromatics in OSPW were proposed to be an important contr

181 ependent on the ratio of NO2(-) to activated aromatics in solution.

182 It appears that the conserved aromatics in the four locations have conserved functions

183 on accepting quinones and possibly condensed aromatics in the high-HTT chars.

184 oA pathway prevents total degradation of the aromatics in the hydrolysate, and instead allows for bio

185 This highlights the importance of suberin aromatics in the polymer's function.

186 On the other hand, polycyclic aromatics, in particular pyrene, are found to induce ord

187 ms meta C-H arylation of a variety of alkoxy aromatics including 2,3-dihydrobenzofuran and chromane w

188 Halogenated homo- and heterocyclic aromatics including disinfectants, pesticides and pharma

189 tobacterium dehalogenans can use chlorinated aromatics including polychlorinated biphenyls as electro

190 Most classes of nitrogen-containing aromatics, including pyridines, quinolines, pyrimidines,

191 o the stationary phase; the hydrogen-bonding aromatics increase the rotational order of homogeneously

192 ential of such reactions in the formation of aromatics increased at a regular pace in the last few ye

193 r biological transformation of this suite of aromatics into selected aromatic compounds potentially r

194 mechanisms for the aqueous dehalogenation of aromatics involving nucleophilic aromatic substitution w

195 have been reported: quinones, viologens, aza-aromatics, iron coordination complexes, and nitroxide ra

196 Pressure-induced polymerization (PIP) of aromatics is a novel method for constructing sp(3) -carb

197 The biosynthesis of aromatics is compromised in cue1, and the reticulate phe

198 Because nitrogen bonded to aromatics is not readily plant-available, this observati

199 ween the Tyr(51)-Phe(64) pair of interacting aromatics is vital to the fold and stability of SUMO.

200 ng four compound classes (alkanes, alcohols, aromatics, ketones), and retention orders were objective

201 to specific aldehydes, alcohols, aliphatics/aromatics, ketones, and amines through the SST1, SST2, S

202 h decreased secondary structure, exposure of aromatics, loss of two coppers, and reduced oxidase acti

203 >/=80%) with low abundances of n-alkanes and aromatics (<5%), similar to "fresh" lubricating oil.

204 mation; [M](+*) for alkanes, ketones, FAMEs, aromatics, [M-H](+*) for chloroalkanes, and [M-H2O](+*)

205 lid soil components with a preference toward aromatics (mainly lignin).

206 d TRPML, suggesting that gate anchoring with aromatics may be common among many TRP channels.

207 obicity of chloro- versus methyl-substituted aromatics may partly explain the general preference for

208 is able to oxidize phenolic and non-phenolic aromatics, Mn(2+), and different dyes.

209 , alcohols, ketones, aliphatic hydrocarbons, aromatics, mono-and sesquiterpenes, oxides/ethers and py

210 erogen (kerogen prefers and sorbs polars and aromatics more than saturates, leading to splitting of o

211 als of different lipid fractions (n-alkanes, aromatics, n-ketones, alcohols, fatty acids and other hi

212 demonstrates a strict specificity for planar aromatics, nonplanar (+/-)-trans-7,8-dihydroxy-7,8-dihyd

213 For chlorinated and brominated aromatics, nucleophilic addition ortho to carbon-halogen

214 The aromatics-off mutant formed dimers and monomers but no t

215 top (lacking 41 C-terminal residues) and the aromatics-off mutants.

216 The seven mutations (aromatics-off) were incorporated into the complete BChE

217 The aromatics-off/C571A mutant yielded only monomers.

218 e formed by the chemisorption of substituted aromatics on metal oxide surfaces in both combustion sou

219 orption interactions of low molecular weight aromatics on MWCNTs.

220 restricting the accessible conformations of aromatics on the surface.

221 Furthermore, conserved aromatics one alpha-helical turn downstream from this po

222 on of biomass-derived furans and alcohols to aromatics over zeolite catalysts.

223 Commonly monitored aromatics (parent and alkylated-polycyclic aromatic hydr

224 detection of Raman signals from coat protein aromatics, particularly tryptophan (W26) and tyrosine re

225 Selectivity to oxygenated aromatics peaks at 350 degrees C while the catalyst is i

226 acement methods and is applicable to (hetero)aromatics, peptides, pharmaceuticals, common monosacchar

227 for interface aliphatics, and that interface aromatics physicochemically contribute to Ail self-assem

228 By linking the ortho-carbons of the aromatics positioned at C-4 and C-5, a fused framework i

229 extra-framework gallium species on enriched aromatics production in zeolite ZSM-5.

230 nophile in this one-pot synthesis, makes the aromatics production much simpler and renewable, circumv

231 These aromatics provide anisotropic shielding to guests, and a

232 trostatic potential surfaces of the relevant aromatics provide useful guidelines for predicting catio

233 ron-rich heteroaromatics and 6-membered ring aromatics provided they had donor groups in the meta pos

234 me that the cyclotrimerization of acetyls to aromatics provides a promising approach to 2D conjugated

235 r acids, organic phosphates, hydroxyl acids, aromatics, purines, and sterols as methoximated and trim

236 ionations of eight pure oils into saturates, aromatics, resins, and asphaltenes (SARA), followed by e

237 Second, the DeOC containing saturates, aromatics, resins, and asphaltenes (SARA), was partially

238 indicated that the oxidation of fluorescing aromatics resulted in the opening of some aromatic rings

239 These aromatics-rich MOFs exhibit an exceptionally high hydrog

240 frameworks (MOFs) were constructed based on aromatics-rich octa-carboxylate ligands and copper paddl

241 thway can retain the aromatic ring of parent aromatics, shedding light on the fact that monocyclic ar

242 the pi-basic pyrene with polarized push-pull aromatics should afford more powerful CPP activators.

243 k of dynamically coupled residues, with some aromatics showing increases in flexibility, which partia

244 ing acetylides, allyl silanes, electron-rich aromatics, silyl enol ethers, and silyl ketene acetals.

245 achieving high-energy in-plane orbitals for aromatics simply by positioning iodine atoms next to eac

246 We used rheology to show that other planar aromatics, some cationic and one neutral dye (methylene

247 results highlight the fact that fluorinated aromatics stand distinct from their chloro- and bromo- c

248 primarily of highly substituted single ring aromatics, substituted furan/pyran moieties, highly bran

249 The VOCs studied here include aromatics such as benzene (1.03 pptv/ppbv CO), toluene (

250 Attempted electrophilic amination of aromatics such as benzene and toluene with methyl- and t

251 While monocyclic aromatics such as benzene were found to disrupt the stru

252 nd third dehydrogenations to form dienes and aromatics such as benzene.

253 ctly grafted, while unsubstituted polycyclic aromatics such as pyrene and perylene have been linked v

254 roups: ketones, aldehydes, amines, alcohols, aromatics, sulfur-containing compounds, phenyls, phenols

255 was formulated to meet a 35% by volume total aromatics target but with a higher octane number.

256 fuels were blended to meet a range of total aromatics targets (15%, 25%, and 35% by volume) while ho

257 ethionine, lysine, isoleucine, arginine, and aromatics, tend to promote stronger cooperative interact

258 include aliphatic hydrocarbons, single ring aromatics, terpenes, chlorinated solvents, formaldehyde,

259 the samples tend to be relatively poorer in aromatics than are meteorites and interplanetary dust pa

260 ncy have identified a variety of chlorinated aromatics that constitute a significant health and envir

261 ituted piperidines and substituted monocylic aromatics that mimic the delta-opioid receptor-ligand bi

262 cceptors; however, attached to electron-poor aromatics, they turn into quite strong donors.

263 any aerobic organisms degrade lignin-derived aromatics through conserved intermediates including prot

264 onger spacer arms that permit their tethered aromatics to adopt alternative orientations in the bindi

265 ligomers by covalently attaching overcrowded aromatics to each other.

266 d oxalic acids confirms the potential of oxy aromatics to produce light-absorbing aqueous secondary o

267 of structurally diverse monocyclic and fused aromatics to the corresponding primary and N-alkyl aryla

268 icles are a potential source of heterocyclic aromatics to the local environment, but other oil sands

269 d provides an example of how the toxicity of aromatics toward microbes can be circumvented by interfa

270 g relatively few interactions with conserved aromatics (Trp672 and Phe673) that are critical for 4E10

271 t defluorination of poly- and perfluorinated aromatics under oxidative conditions catalyzed by the mu

272 ed as solvent for electrophilic nitration of aromatics using a variety of nitrating systems, namely N

273 fication and ring opening of the single-ring aromatics vanillate and 3-O-methylgallate, which are com

274 r the detection of high explosives and other aromatics via a fluorescence quenching and enhancement m

275 application to oxidative cross-couplings of aromatics via decarboxylative/C-H or double decarboxylat

276 rmal aromatic C-H insertion on electron-rich aromatics was also achieved.

277 The selectivity towards C2 or aromatics was manipulated purposely by adding H2 into or

278 erial strain that metabolizes lignin-derived aromatics, was previously available.

279 guest molecules as opposed to planar, rigid aromatics, was synthesized via the Weak-Link Approach.

280 imuli, while carboxylic acids and aliphatics/aromatics were comparatively less effective in eliciting

281 Relative concentrations of heterocyclic aromatics were estimated and were found to decrease with

282 idation, two-ring and three-ring fluorescing aromatics were preferentially removed at doses <100 mg/L

283 oved at doses <100 mg/L Fe(VI), and one-ring aromatics were removed only at doses >/=100 mg/L Fe(VI).

284 yproducts, that is, alkenes, oxygenates, and aromatics, were not present in significant amounts.

285 unced when cysteine replaces the interfacial aromatics, which are known to participate in tertiary in

286 The chemistry works best with electron-rich aromatics, which is in agreement with the idea that thes

287 it could help satisfy increasing demand for aromatics while filling the gap created by decreased pro

288 y free of diaryl ketones by carboxylation of aromatics with a carbon dioxide-Al(2)Cl(6)/Al system at

289 thway provides insight into the reactions of aromatics with Ca that are relevant in the areas of cata

290 on C-H functionalization of diverse (hetero)aromatics with dibenzothiophene-S-oxide followed by the

291 ronic esters can be coupled to electron-rich aromatics with essentially complete enantiospecificity.

292 otifs were also incorporated into polycyclic aromatics with five or six rings in the main backbone, a

293 amination of a variety of simple and complex aromatics with heteroaromatic azoles of interest in phar

294 ion is mandatory for label-free detection of aromatics with high sensitivity.

295 -interface membrane-proximal external region aromatics with hydrophobic residues of the transmembrane

296 result from the interaction of the oxidized aromatics with metal ion centers.

297 omatics with triethylsilane and nitration of aromatics with metal nitrate.

298 Methylation of aromatics with the (CH3)3O+CF3SO3- in CF3SO3H and 2CF3SO

299 ionic hydrogenation of various ketones, and aromatics with triethylsilane and nitration of aromatics

300 ssisted aerobic oxidative C-H olefination of aromatics with unactivated alkenes has been developed.