ライフサイエンスコーパス: aromatic

1 lysis, focusing mainly on other heterocyclic aromatics.

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

3 4,6-cyclooctatriene (C8 H8 ) and the triplet aromatic 1,3,5,7-cyclooctatetraene (C8 H8 ).

4 classical organic chemistry the triplet non-aromatic 2,4,6-cyclooctatriene (C8 H8 ) and the triplet

5 -H benzoxylation of tertiary benzamides with aromatic acids by weak O-amide coordination in the prese

6 NO conversion mediated by vitamins C, E, and aromatic alcohols has been recently shown to be feasible

7 ly synthesized homopropagylic or homoallylic aromatic alcohols in the presence of nitriles has been e

8 ecognition of a wide variety of aliphatic or aromatic aldehydes and ketones, as demonstrated by hiera

9 A good range of aromatic aldehydes is selectively labeled, and a one-pot

10 study of nickel-catalyzed decarbonylation of aromatic aldehydes under relatively mild conditions.

11 -pot three-component reaction of arylamines, aromatic aldehydes, and cyclic ketones was described for

12 lied to the efficient preparation of diverse aromatic aldehydes.

13 s (up to >20:1 E/Z) in high selectivity with aromatic, alpha,beta-unsaturated, and aliphatic aldehyde

14 ures, we have explored the effect of bending aromatic amide beta-sheets using building blocks that im

15 understanding of the covalent interaction of aromatic amine metabolites with protein nucleophiles.

16 aved to provide 2 equiv of the corresponding aromatic amine.

17 14 amines including the two potent mutagenic aromatic amines 2,3- and 2,8-phenazinediamine, which wer

18 le DNAN is known to biotransform in soils to aromatic amines and azo-dimers, it is seldom mineralized

19 ed it highly efficient for the extraction of aromatic amines in a wide polarity range (log Kow values

20 d data evaluation methods aiming to identify aromatic amines in six mutagenic wastewater effluents fr

21 Detection limits for aromatic amines in textiles (0.007-2 mg kg(-1)) were wel

22 ds also contributed to the mutagenicity when aromatic amines were present.

23 especially important in the case of (hetero)aromatic amines-essentially a one-pot reaction with no i

24 All the analyzed samples were positive in aromatic amines.

25 ters with a possible link to the presence of aromatic amines.

26 ro-l-m-tyrosine ([(18)F]FMT; a substrate for aromatic amino acid decarboxylase), baseline D2/3 recept

27 by which plants maintain intercompartmental aromatic amino acid homeostasis, and provide critical in

28 d multifaceted intercompartmental effects on aromatic amino acid metabolism.

29 rimental effects of hyperaccumulation of the aromatic amino acid phenylalanine (Phe) in animals, know

30 associated benzene rings (a simple model of aromatic amino acid side chains) can switch inherent dyn

31 t such interactions are possible for all the aromatic amino acid side-chains.

32 nscriptional activation of genes involved in aromatic amino acid, S-adenosyl methionine (SAM) and fol

33 ating branched-chain amino acids (BCAAs) and aromatic amino acids (AAAs) have been shown to be associ

34 All three aromatic amino acids (tryptophan, phenylalanine and tyro

35 Herein, we use two unnatural aromatic amino acids and several spectroscopic technique

36 had reduced urine levels of methylamines and aromatic amino acids metabolites.

37 of carbon flux toward the shikimate-derived aromatic amino acids tyrosine and tryptophan.

38 resence of a flexible loop region containing aromatic amino acids, the caveolin-binding motif.

39 sequence enriched in positively charged and aromatic amino acids.

40 and contained multiple large hydrophobic and aromatic amino acids.

41 hin C reveals a distinct approach to install aromatic amino groups in metabolites and raises question

42 s ability to efficiently oxidize an array of aromatic and aliphatic aldehydes, including the reactive

43 Both aromatic and aliphatic carboxylic acids were converted t

44 Aromatic and antiaromatic molecules-which have delocaliz

45 s suggests the existence of polycarboxylated aromatic and condensed aromatic formulas, with CHON-type

46 investigations were carried out on both its aromatic and disulfide forming amino acids.

47 e replacement of a CH group with a N atom in aromatic and heteroaromatic ring systems can have many i

48 under mild conditions and engage a range of aromatic and heteroaromatic systems present in the barbi

49 Several aromatic and hydrophobic residues in pore helix 1, helic

50 Active layers of two fully aromatic and two semi-aromatic nanofiltration membranes

51 in this protocol can be further reacted with aromatic and vinyl halides, under palladium catalysis, t

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

53 nized by LDI can be classified as aliphatic, aromatic, and condensed aromatics in approximately equal

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

55 show that the cohesive properties of simple aromatic- and lysine-rich peptides rival those of the st

56 Both aliphatic and aromatic anhydrides are formed on convenient time scales

57 ult in supramolecular hydrogels upon mixing, aromatic-aromatic interactions promote the pentapeptides

58 ing helical segments flanking a central bent aromatic beta-sheet were then synthesized and shown to f

59 oxylic acids after oxidative cleavage of the aromatic bond with two vicinal hydroxy groups to yield s

60 roteins synthetically modified with a simple aromatic boronate motif are actively trafficked to the n

61 ps occupying the electron-rich cavity of the aromatic bowl.

62 oiety of its substrates via an NPP7-specific aromatic box composed of tyrosine residues.

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

64 d regioselective ortho-specific nitration of aromatic C(sp(2))-H bonds using chelation-assisted remov

65 um-catalyzed enantioselective borylations of aromatic C-H bonds.

66 o reactions involving the cleavage of strong aromatic C-O bonds.

67 ses reveal that these CCHs share a conserved aromatic cage for the hydrolytic activity.

68 ugh all such reader proteins bind Kme3 in an aromatic cage, the driving force for binding may differ;

69 A library of aromatic carbamate derivatives based on the clinically a

70 ing carboxylates and that the enhancement of aromatic carbonates is more pronounced indicates that th

71 ated in TS and that TS preferentially buries aromatic carbons and amide nitrogens while leaving amide

72 ost Coulombic interactions of RO and burying aromatic carbons.

73 e water samples that is capable of oxidizing aromatic carboxylates.

74 ma-bond metathesis of silylated alkynes with aromatic carboxylic acids on the Ag(111) and Au(111) sur

75 lecules CO2 (44 Da) and C2H6O2Si (90 Da) for aromatic carboxylic acids.

76 toinduced decarboxylation of redox-activated aromatic carboxylic acids.

77 The elaboration of the resorcin[4]arene's aromatic cavity produced a self-folding, deep hexaamide

78 n aromatic pi orbital rather than toward the aromatic centroid.

79 explore how the fusion of benzene rings onto aromatic chameleonic units represented by biphenylene, d

80 o compounds have a relatively high amount of aromatic character.

81 prehensive understanding of local and global aromatic characters of various rings in fused ring syste

82 cteristic sweetness, and improved colour and aromatic complexity.

83 e investigated in order to: i) elucidate the aromatic composition by means of HS-SPME coupled with GC

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

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

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

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

88 Aromatic compounds are environmental pollutants with tox

89 nsights into fundamental questions about how aromatic compounds behave.

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

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

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

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

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

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

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

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

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

99 amination of nitrogenous and non-nitrogenous aromatic compounds.

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

101 ogy efforts to valorize previously underused aromatic compounds.

102 condensation products, named trace-extended aromatic condensation products (TEACOPs), which are acti

103 These bonds extend aromatic conjugation into the combined graphene oxide sh

104 d oxygen-containing heterocycles, as well as aromatic-containing pharmaceutical agents.

105 Alkenes and aromatics contributed to the largest fractions of photoc

106 bstitution pattern of the polyketide-derived aromatic core that seemingly contradicts the established

107 embedding of a compensating charge within an aromatic cyclononatetraenide ring by the symmetric super

108 to protocatechuate, a common intermediate of aromatic degradation pathways.

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

110 es exhibit remarkably high reactivity toward aromatic diazonium ions and this reaction can be used to

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

112 emporal storage or even sink for terrigenous aromatic DOM compounds.

113 Based on specific UV-absorption (SUVA), aromatic DOM was preferentially adsorbed.

114 ls available for overcoming the considerable aromatic energies inherent to these building blocks limi

115 (linear or branched at the alpha-carbon) and aromatic ester groups have been synthesized, their solid

116 ive in promoting the reductive hydrolysis of aromatic ethers in aqueous phase at relatively mild temp

117 bly of short o-phenylenes, a simple class of aromatic foldamers, into twisted macrocycles.

118 quantum yields, as waters enriched in highly aromatic formulas exhibit much higher rates of light abs

119 e of polycarboxylated aromatic and condensed aromatic formulas, with CHON-type COO KMD formulas relat

120 The aromatic fractions of snow, lake sediment, and air sampl

121 The highly distorted aromatic framework with alternating out-of-plane substit

122 Twisted two-dimensional aromatic frameworks have been prepared by overcrowding t

123 e or monophosphonate groups are masked by an aromatic group and an amino acid ester moiety, which are

124 f the electron-donating character of (hetero)aromatic group attached to the alkenyl moiety.

125 to form stacking and NH-pi interactions with aromatic groups of proteins.

126 the QA and form weaker interactions with the aromatic groups.

127 erved for thiols, sulfides, and alkenes over aromatic groups.

128 With aromatic guest-host peptides, the 50% conducting interme

129 A variety of aromatic, heteroaromatic, and alkyl carboxaldehydes were

130 Five-membered aromatic heterocycles are a ubiquitous skeleton of pi-co

131 Recently, it was reported that C-H bonds in aromatic heterocycles were converted to C-Si bonds by re

132 um gilvum VM552 served as a model polycyclic aromatic hydrocarbon (PAH) degrading bacterium.

133 soils of broad pH (4.26-8.43) and polycyclic aromatic hydrocarbon (PAH) gradients (0.18-20.68 mg kg(-

134 Interaction between polycyclic aromatic hydrocarbon (PAH) molecule and energetic ion is

135 t approach currently employed for polycyclic aromatic hydrocarbon (PAH)-contaminated media, wherein c

136 by oxidation with DDQ, afforded a polycyclic aromatic hydrocarbon (PAH)-porphyrin hybrid in 38% yield

137 onal synthesis of cyclopentafused-polycyclic aromatic hydrocarbon embedded ladder polymers using a pa

138 eas, and other amides by osmometry and amide-aromatic hydrocarbon interactions by solubility.

139 Interestingly, retene, a polycyclic aromatic hydrocarbon present in PM10, is a potential com

140 d oligomers featuring a nonplanar polycyclic aromatic hydrocarbon, corannulene, and a planar aromatic

141 Benzo[a]pyrene (BaP), a polycyclic aromatic hydrocarbon, is the major cause of lung cancer.

142 l, gas + particle-associated) for polycyclic aromatic hydrocarbons ( summation operator13 PAHs) were

143 Particulate polycyclic aromatic hydrocarbons (p-PAHs) emitted from diesel vehic

144 istance to a ubiquitous pollutant-polycyclic aromatic hydrocarbons (PAH).

145 Protection Agency (EPA)-priority polycyclic aromatic hydrocarbons (PAHs) adsorbed on LCPM from therm

146 Syntheses of large polycyclic aromatic hydrocarbons (PAHs) and graphene nanostructures

147 Polycyclic aromatic hydrocarbons (PAHs) are widely distributed thro

148 g to rationalize the formation of polycyclic aromatic hydrocarbons (PAHs) as detected in carbonaceous

149 his study aimed at evaluating the polycyclic aromatic hydrocarbons (PAHs) contamination of commercial

150 tic pollutants that co-occur with polycyclic aromatic hydrocarbons (PAHs) in contaminated soils.

151 To assess the exposure to polycyclic aromatic hydrocarbons (PAHs) it is important to understa

152 important sources of exposure to polycyclic aromatic hydrocarbons (PAHs), a group of organic chemica

153 nown for their ability to degrade polycyclic aromatic hydrocarbons (PAHs).

154 d aromatics (parent and alkylated-polycyclic aromatic hydrocarbons and dibenzothiophenes) were exclud

155 Polycyclic aromatic hydrocarbons are important structural motifs in

156 btained mass spectra of five pure polycyclic aromatic hydrocarbons as well as complex petroleum sampl

157 cedure for the photooxidation of a family of aromatic hydrocarbons by a phosphate-bearing flavin mono

158 gradation at 0 degrees C (1000 m), where the aromatic hydrocarbons fluoranthene, anthracene, and Dibe

159 ted with environmental exposure to gasoline; aromatic hydrocarbons from refinery pollution, petroleum

160 bic guests, including fullerenes, polycyclic aromatic hydrocarbons, and steroids, with subtle differe

161 enerate fractions of saturated hydrocarbons, aromatic hydrocarbons, basic compounds, naphthenic acids

162 Polycyclic aromatic hydrocarbons, major constituents of DEPs, were

163 ds (levoglucosan and resin acids, polycyclic aromatic hydrocarbons, nicotine) in the mass spectra wer

164 ting from shale formations (e.g., polycyclic aromatic hydrocarbons, phthalates), fracturing fluids (e

165 e substituted and non-substituted polycyclic aromatic hydrocarbons.

166 y, whereas simultaneous substitution of four aromatic/hydrophobic residues with Ala dramatically impa

167 amics simulations, here we identified single aromatic/hydrophobic residues within the amyloid core IA

168 with a substrate bearing both aliphatic and aromatic hydroxy groups the enzyme preferentially silyla

169 [Ni(III) (mu-O)2 Co(III) ](2+) core through aromatic hydroxylation reactions represent a new domain

170 its 4+ oxidation state (80 pi electrons) and aromatic in its 6+ oxidation state (78 pi electrons).

171 These acceptor molecules are generally aromatic in nature and mostly indole or indole-like.

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

173 ts to improve the production of biofuels and aromatic industrial products as well as increase disease

174 cial; this study explores the nature of urea-aromatic interactions relevant in urea-assisted protein

175 an extended beta-sheet structure, as well as aromatic interactions.

176 The results demonstrate that (aromatic) ketones/aldehydes, as opposed to quinones, pla

177 T/nectin-2 interaction and revealed that an "aromatic key" of nectin-2 is critical for this interacti

178 Aromatic l-amino acid decarboxylase (AADC) deficiency is

179 F110 up-regulates tyrosine hydroxylase (TH), aromatic l-amino acid decarboxylase (AADC), and GTP cycl

180 ericytes that ectopically express the enzyme aromatic L-amino acid decarboxylase (AADC), which synthe

181 ertion into a C horizontal lineC bond of its aromatic ligand framework to give silacycloheptatriene (

182 to 2017 concerning the organic reactions of aromatic ligands eta(2)-coordinated to tungsten or molyb

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

184 te feed composition indicate that both fully aromatic membranes achieved similar rejection despite th

185 tion, and quantum mechanical calculations on aromatic model systems reveal that such interactions are

186 s of main-chain boron-containing CPs without aromatic moieties within the polymer backbone, potential

187 udied in different size regimes: the largest aromatic molecules have diameters of about one nanometre

188 reduction processes in a series of different aromatic molecules.

189 hydroarylation of dienes with electron-rich aromatic molecules.

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

191 et motif of a protein, being connected to an aromatic motif (i.e., pyrene) at their C-terminal, self-

192 ve layers of two fully aromatic and two semi-aromatic nanofiltration membranes were studied along wit

193 action cannot be functionally substituted by aromatic, non-polar, or polar sidechains.

194 diation, typical mono- and multi-substituted aromatic olefins could be converted into ketones and ald

195 ulation of aryl ketones with a wide range of aromatic olefins under ambient air in good yields.

196 Well-defined, fused-ring aromatic oligomers represent promising candidates for th

197 A series of aromatic-paneled Fe(II)4L6 cages was synthesized through

198 eference for a ligand conformation where the aromatic panels lie tangent to the edges of the tetrahed

199 Cages with large, offset aromatic panels were observed to be the most effective h

200 Both the size and arrangement of the aromatic panels were shown to be crucial for achieving e

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

202 perties of those substituents, and secondary aromatic pharmacophores can enhance agonist efficacy for

203 hydroxyl group and, then, by addition of one aromatic phenol carbon to the carbon-carbon double bond

204 ing the meta-position of anilines to produce aromatic phosphonium ions or phosphonates.

205 he S-H sigma* toward the ring carbons and an aromatic pi orbital rather than toward the aromatic cent

206 1,4-Disubstituted aromatic piperazines are privileged structural motifs re

207 nt solvent system types, including nonpolar, aromatic, polar, and hydrogen bonding solvents.

208 The aromatic polyimide, which is more rigid due to the stron

209 The kinamycin family of aromatic polyketide natural products contains an atypica

210 two-electron oxidation of isophlorin to the aromatic porphyrin.

211 Low pungency, high aromatic potential and red color, give to Piper borbonen

212 By knowing the aromatic profile of a food, one can understand the natur

213 However, amino acid and aromatic profiles were mostly affected by climate condit

214 s area provide fundamental insights into the aromatic properties, tautomerization, and reactivity of

215 ution (12% v/v) and 1083microg/L in a fruity aromatic reconstitution, reflecting its presence in wine

216 teraction between the ligand and a conserved aromatic residue in the ligand-binding pocket.

217 ervations suggest that intercalation by this aromatic residue is one of the earliest steps in the sea

218 ng adaptor depends on a network of polar and aromatic residues along the length of the TM domain.

219 dinium, can preferentially accumulate around aromatic residues and that tetrapropylammonium undergoes

220 nct changes in the electronic environment of aromatic residues in this peptide compared to that of th

221 we performed alanine scanning mutagenesis of aromatic residues located in transmembrane helices II, I

222 We found that aromatic residues, especially Trp, and sulfur-containing

223 ture is formed by intermolecular stacking of aromatic residues, which would spatially constrain the k

224 ture of the EBOV FL through several critical aromatic residues.

225 onnector loop containing a conserved trio of aromatic residues.

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

227 in consistent proportions in a set of elite aromatic rice varieties from South East Asia and Austral

228 ntacts, and hydrogen bonds and specific atom-aromatic ring (cation-pi, donor-pi, halogen-pi, and carb

229 halogen-pi, and carbon-pi) and aromatic ring-aromatic ring (pi-pi) interactions, within user-submitte

230 ine strengthens the interaction between this aromatic ring and both ACh and choline.

231 gnificant preference for the centroid of the aromatic ring and distances near the sum of the van der

232 These results suggest a path for aromatic ring formation in cold acetylene-rich environme

233 ting group to the meta and ortho sites on an aromatic ring in its first excited singlet state.

234 energy and stabilize products including the aromatic ring of the benzene cation.

235 epends on the pi-pi interactions between the aromatic ring of the C-2 protecting group with the exocy

236 of the transition states, we found that the aromatic ring of the phenyl aliphatic amines may form ca

237 Delocalized pi electrons in aromatic ring structures generally induce diamagnetism.

238 umber, number of oxygen atoms, and number of aromatic ring structures, lead to over fit models, and a

239 pi, donor-pi, halogen-pi, and carbon-pi) and aromatic ring-aromatic ring (pi-pi) interactions, within

240 ignificantly contribute to alkylation at the aromatic ring.

241 ne subpocket of the AcCoA binding site by an aromatic ring.

242 ridinyl ring of 2 could be replaced by other aromatic rings and the pyrrolidinyl ring is not required

243 ribac, a member of the PYBs, possesses three aromatic rings and these adopt a twisted "S"-shaped conf

244 When the aromatic rings are modified with electron donating (with

245 ens show a common scaffold consisting of two aromatic rings connected by a linear or a cyclic spacer.

246 While substitution on the aromatic rings had comparatively little effect on quadri

247 ir widespread use to forge bonds between two aromatic rings has enabled every branch of chemical scie

248 at occurs between the toluene and the N-oxyl aromatic rings in the transition state structures.

249 vely and efficiently fusing large numbers of aromatic rings, yet such methods remain scarce.

250 tegies for the electrophilic substitution of aromatic rings.

251 tral compounds containing one, two, or three aromatic rings.

252 dorsing the inorganic benzene as a versatile aromatic scaffold for engineering of molecular materials

253 sn-X-Ser/Thr (NXS/T) sequon and the enhanced aromatic sequons (Phe-X-Asn-X-Thr and Phe-X-X-Asn-X-Thr)

254 We then introduced the optimized-enhanced aromatic sequons into other glycoproteins and observed a

255 gular quinoxalenediynes due to gain of a new aromatic sextet.

256 Orientations of aromatic side chains of these complexes are distinctive,

257 es was essentially investigated with peptoid aromatic side chains, among which the chiral 1-naphthyle

258 nium chloride can specifically interact with aromatic side chains.

259 stinct sub-states characterized by different aromatic side-chain conformations at the RNA-binding sur

260 t states and that a conformational switch of aromatic side-chains fine-tunes sequence specific bindin

261 In contrast, in aromatic solvents folding of the macrocycles with a dist

262 Studies in a variety of aromatic solvents indicate that these solvents embed bet

263 sed n-sigma* hydrogen bond) and amide sp(2)O-aromatic sp(2)C (proposed n-pi*) interactions are favora

264 Naphthalene results show that aromatic sp(2)C-amide sp(2)N interactions in water are u

265 an cyclization irreversible due to favorable aromatic stabilization energy, while extended linear ben

266 y, we validate the ubiquitous nature of urea-aromatic stacking interactions by analyzing experimental

267 ntiaromatic) and a stabilized triplet (Baird aromatic) state.

268 However, due to the ultra-flat aromatic structure of SN-38, it is typically very diffic

269 r of common organic functional groups (e.g., aromatic substituents, halides, isolated mono- and di-su

270 cts are also formed as a result of competing aromatic substitution (Friedel-Crafts reaction).

271 Nucleophilic aromatic substitution (SNAr) is a direct method for aren

272 oride salts for applications in nucleophilic aromatic substitution (SNAr) reactions.

273 y predictions for the important nucleophilic aromatic substitution class of reactions.

274 c route to arylazoindazoles via nucleophilic aromatic substitution is presented.

275 The electrophilic aromatic substitution of a C-H bond of benzene is one of

276 oethers) via an organocatalyzed nucleophilic aromatic substitution of silyl-protected dithiols.

277 Here we perform an abiotic electrophilic aromatic substitution reaction, which is directed precis

278 tic halogenation reactions range from simple aromatic substitutions to stereoselective C-H functional

279 ylation is facile with partially fluorinated aromatic substrates containing two ortho fluorine substi

280 COFs) to date are made from relatively small aromatic subunits, which can only absorb the high-energy

281 y may allow the incorporation of even larger aromatic subunits.

282 ng interactions with more electron-deficient aromatic surfaces.

283 -pi interactions between protic solvents and aromatic surfaces.

284 iments were also performed on pyridine(polar-aromatic)-swelled kerogen.

285 The inclusion of nitrogen into an aromatic system and their growth can fill the mechanisti

286 The NBO analysis shows that the aromatic system is delocalized.

287 tic chain or a chain carrying an appropriate aromatic system, such as the biphenyl system, and a free

288 For example, highly aromatic, tannin-like formulas correlate positively with

289 based N-phenylbenzoxazine with aliphatic and aromatic thiols was investigated in solvent-mediated and

290 so that they can be changed from diatropic ('aromatic') to paratropic ('antiaromatic') simply by chan

291 Lalat, an aromatic traditional rice variety, with 2.91% RS and 27.

292 ative of the formation of the corresponding "aromatic triplet" species according to the Baird's rule

293 matic hydrocarbon, corannulene, and a planar aromatic unit, thiophene, is synthesized through an iter

294 However, as the aromatic units are moved along the peptide backbone away

295 Positioning the aromatic units close to the N-terminus of the peptide ba

296 Furthermore, sesame oil containing aromatic volatiles and compounds with different polariti

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

298 this study suggest these phenolic and nitro-aromatic will partition into the condensed state for a w

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

300 ue comes with the larger contribution of the aromatic zwitterionic mesomeric form.