ライフサイエンスコーパス: aniline

1 hols, phenols, carboxylic acids, amines, and anilines).

2 nitrosobenzene (NOB), metabolic products of aniline.

3 enus, demonstrated the assimilation of (13)C-aniline.

4 f excited triplet and singlet states of 4-Cl-aniline.

5 r metabolism-based unmasking of the embedded aniline.

6 along with the corresponding aryldiazene and aniline.

7 opargylic hydrogen and a protonated tertiary aniline.

8 )Fe3(thf) affords ((tbs)L)Fe3(mu(3)-NPh) and aniline.

9 d utilizing 2,6-bis(diphenylmethyl)-4-methyl aniline.

10 pollutants like NB and in the production of aniline.

11 sional geometry adopted by the F12SubPc-TCBD-aniline.

12 the phenol could be highly favored over the aniline.

13 mett sigmap(+) parameter of the incorporated aniline.

14 rephthalaldehyde and differently substituted anilines.

15 d(II)-templated self-assembly with different anilines.

16 with electronically neutral or electron-rich anilines.

17 the condensation of 2-acyl-benzaldehydes and anilines.

18 ra reaction and (B) the radical arylation of anilines.

19 derivatives with expulsion of p-substituted anilines.

20 for the direct substitution of alcohols with anilines.

21 f primary and secondary aliphatic amines and anilines.

22 ectron-rich hydroxy- and methoxy-substituted anilines.

23 ysts for the hydrogenation of nitroarenes to anilines.

24 ized means for preparing aryl fluorides from anilines.

25 hat can further be hydrolyzed to halogenated anilines.

26 followed by derivatization of the so formed anilines 14 gave the N-alkyl-(15a-c), N-acyl-(16a,b and

27 ed various electrografting conditions of two anilines (2-[(4-aminophenyl)sulfanyl]-8-hydroxy-1,4-naph

28 inone methide, which is intercepted by boryl aniline 31 to forge a new C-N bond.

29 The key step involved the union of boryl aniline 31 with brominated murrayaquinone A (26).

30 The transformation of aniline, 4-CH3-, 4-OCH3-, and 4-Cl-aniline by excited tr

31 Here we demonstrate that the addition of aniline (a weak base) can control the acidity of PEDOT:P

32 etabolic site leading to the formation of an aniline, a structural motif of prospective safety concer

33 catalyzed aminations of aryl halides to form anilines, a common structure found in drug agents, natur

34 i-tert-butyl-N-(3,5-di-tert-butylbenzylidene)aniline (abbreviated as TBI for tetra-tert-butyl imine),

35 d to be general for a wide range of anisole, aniline, acetanilide, and phenol derivatives and allowed

36 ent chlorination of a wide range of anisole, aniline, acetanilide, and phenol derivatives.

37 ese salen catalyst followed by trapping with aniline afforded the urea product in 51% enantiomeric ex

38 formed directly from commercially available anilines, aldehydes, and alkynes bearing a variety of su

39 Anilines, aliphatic amines, alpha-chiral aliphatic amine

40 ly, the in situ diazotization of a number of anilines allows the directional synthesis of desired 3-s

41 d not be explained by the speciation of 4-Cl-aniline alone.

42 this reaction with secondary free amines and anilines also overcomes the limitations of palladium(II)

43 stants for the functional groups para to the aniline amine were plotted versus the wavenumber (cm(-1)

44 Aniline (AN) and diphenylamine (DPA) are examples of tox

45 hesized by electrochemical polymerization of aniline and 3-aminobenzoic acid, in the presence of a di

46 nergy barrier of the reactions revealed that aniline and aliphatic amines (e.g., methylamine) prefer

47 anthridinone synthesis using the coupling of aniline and amide by formation of C-C and C-N bonds in a

48 transformation demonstrates a broad range of aniline and amide substrates with different functional g

49 is based on the Stenhouse reaction in which aniline and furfural react in acidic media with the gene

50 so accurately predicted sorption behavior of aniline and imidazole between pH 3 and 10.

51 h more challenging coupling partners such as aniline and ketones.

52 nt preparation of 1,2-dihydroquinolines from aniline and phenyl acetylene.

53 as developed from classical spot tests using aniline and phenylhydrazine dyes that enable molecular r

54 Although aniline and pyridine derivatives interact with His342, b

55 the excited state between the electron-rich aniline and the F12SubPc pi-surface, two molecular fragm

56 The DNAzyme catalyzes the polymerization of aniline and the hybridized miRNA strands guide the depos

57 nes via a multicomponent reaction between an aniline and two ketones is described.

58 substrate and is active with amines such as aniline and veratrylamine as well as sulfhydryl compound

59 pivaloyl oximes to the corresponding primary anilines and 1-aminonaphthalenes.

60 tereocontrol in a single step from secondary anilines and aldehydes possessing a pendent dienophile.

61 nds have become useful methods to synthesize anilines and aniline derivatives, an important class of

62 Various anilines and aromatic as well as aliphatic aldehydes are

63 hioureas obtain by reacting 2-(phenylethynyl)anilines and aryl isothiocynates undergo efficient casca

64 Through the study of substituted anilines and benzylamines, we demonstrated that cooperat

65 meta-C-H bonds--as far as 11 bonds away--of anilines and benzylic amines.

66 ubtle selectivities imposed by the different anilines and counterions employed.

67 rt the first straight access to indoles from anilines and ethylene glycol by heterogeneous catalysis,

68 iazine ring, including pyrazolyl-substituted anilines and o-, m-, and p-phenylenediamine as pi-conjug

69 ld and efficient oxidant for the coupling of anilines and o-aminophenols on protein substrates.

70 rovides one-step synthetic access to primary anilines and phenols at low temperature and avoids the u

71 Pd-catalyzed meta-C-H chlorination of anilines and phenols is developed using norbornene as th

72 n the presence of functional groups, such as anilines and phenols, which are also known to undergo pa

73 on, (ii) N-cyanomethylation of the secondary aniline, and (iii) one-pot mesylation followed by ring c

74 or on a scale similar to that of thiophenol, aniline, and amine groups but not as that of hydroxyl.

75 r 4-OCH3-aniline to 1.0035+/-0.0006 for 4-Cl-aniline, and correlated well with the electron donating

76 -nitroperchloro-1,3-butadiene and para-nitro aniline, and generated the potential energy profiles wit

77 hile no Cl was detected in MnOx-phenol, MnOx-aniline, and MnOx-control.

78 on of manganese oxide [MnOx(s)] with phenol, aniline, and triclosan in batch experiments using X-ray

79 elective access to synthetically challenging anilines, and addresses long-standing issues associated

80 nent coupling reactions of nitrodiazoesters, anilines, and aromatic nucleophiles, thereby preparing a

81 eved by exploiting readily available amines, anilines, and bisphenols as starting materials.

82 lpha,alpha-diarylacetates featuring indoles, anilines, and other electron-rich aromatics.

83 ence controlled, DNA-conjoined copolymers of aniline (ANi) and 2,5-bis(2-thienyl)pyrrole (SNS) were s

84 On the basis of our recently reported aniline aqueous borylation, molecular diversity was achi

85 ions of substituted 2-allyl-N-(2-bromobenzyl)anilines are described.

86 Diversely substituted anilines are prepared by treatment of functionalized ary

87 ed trishydrazide--in the presence of acid or aniline as catalyst, the kinetics of gelation can be tun

88 tridentate pincer ligand containing pendent anilines as hydrogen bond donor groups in the secondary

89 Using indoles and anilines as nucleophiles, the reaction leads to the form

90 ve addition based on the recent discovery of anilines as outstanding substrates for radical arylation

91 ry amines, including fluoroalkyl-substituted anilines as well as the bioactive compound Cinacalcet HC

92 , which were prepared from the corresponding anilines, as aryl radical sources, a range of 3-hydroxy-

93 Cs(+) as a quencher of excited singlet 4-Cl-aniline at pH 7.0 and 9.0.

94 pes associated with anaerobic degradation of aniline at this complex industrial site, which suggests

95 were observed to displace electron-deficient anilines at the dynamic-covalent imine bonds of these ca

96 bituric acid "acceptors" in combination with aniline-based "donors" an absorption range spanning from

97 with a [24]crown-6 (24C6) macrocycle and an aniline-based axle with terminal pyridine donor groups.

98 Aniline-based copolymer, modified with the nanomaterials

99 studies elucidated the binding site of these aniline-based influenza fusion inhibitors, which signifi

100 ing established acetohydrazide approaches to aniline-based methods, and finally to optimized p-toluid

101 ortho:meta regioselectivities, now even for anilines bearing a donor substituent in the para positio

102 e describe the transformation of halogenated anilines, benzonitriles, phenols, methoxylated, or hydro

103 Anaerobic aniline biodegradation was investigated under different

104 th PDLP1-green fluorescent protein (GFP) and aniline blue (a stain for callose normally observed at p

105 GLS1 overexpression, live-cell imaging, and aniline blue fluorochrome staining.

106 nstrated by Safranin O, Picrosirius red, and aniline blue staining.

107 erformed by Safranin O, Picrosirius red, and aniline blue staining.

108 precipitation, and 3,3'-diaminobenzidine and aniline blue staining.

109 ethylene glycol) derivative of benzothiazole aniline, BTA-EG4, is a novel amyloid-binding small molec

110 ethylene glycol) derivative of benzothiazole aniline, BTA-EG4, on tau.

111 mation of aniline, 4-CH3-, 4-OCH3-, and 4-Cl-aniline by excited triplet states of the photosensitizer

112 We report the synthesis of fluorinated anilines by palladium-catalyzed coupling of fluoroalkyla

113 symmetric triarylmethanes bearing secondary anilines by ytterbium-catalyzed Friedel-Crafts reaction

114 me formations performed under stoichiometric aniline catalysis.

115 Assisted by Kool's aniline catalyst, the reaction conditions can be both pH

116 tuted carbene insertion into the N-H bond of aniline catalyzed by readily available copper salt under

117 e reaction considerably over the traditional aniline-catalyzed reaction at neutral pH.

118 zene)RuCl(4-methoxy-N-(2-quinolinylmethylene)aniline) ]Cl (4) displayed low micromolar IC50 values in

119 tropolymerization a conductive polymer poly-(aniline-co-3-aminobenzoic acid) (PANABA) then we immobil

120 MGC) that was electrodeposited within a poly(aniline-co-meta-aminoaniline) electroconductive polymer

121 anoparticles, glucose oxidase (GOD) and poly[aniline-co-N-(1-one-butyric acid) aniline] (SPAnH) were

122 00 in N-Methylaniline and by factor of 80 in Aniline compared to the expected values in the case of b

123 ctors affecting the sensor sensitivity (i.e. aniline concentration, scan number and scan rate of elec

124 ucture of one atropisomer of each SubPc-TCBD-aniline conjugate has been solved, allowing to unambiguo

125 Each of the two SubPc-TCBD-aniline conjugates presents a unique photophysical featu

126 Substituted anilines containing a sulfonyl group may be oxidized in

127 Thereby, meta-alkylated anilines could be accessed, which are difficult to prepa

128 on both the boronate ester substrate and the aniline coupling partner under the reaction conditions.

129 (13)C- and (15)N-AKIE-values of 2-Cl-aniline decreased in the presence of Cs(+), whereas thos

130 bacterium album was identified as a dominant aniline degrader as indicated by incorporation of (13)C-

131 The identification of novel putative aniline degraders expands current knowledge regarding th

132 ovorax spp. were also identified as putative aniline degraders in both of these two treatments, indic

133 Furthermore, the aniline degrading phylotypes identified in the current s

134 e current study are not related to any known aniline-degrading bacteria.

135 GAL capture antibodies to electropolymerized aniline deposited on top of an electrosprayed graphene/p

136 Reduction of NO2 in 1e led to aniline derivative 1t, which was reductively alkylated w

137 The application of an ortho-aniline derivative as a protective group was demonstrate

138 alyzed reduction of the NO2 group led to the aniline derivative, which was acylated.

139 spectroscopic properties of three different aniline derivatives (aniline, N,N-dimethylaniline, and N

140 ansformations with tertiary alkyl halides on aniline derivatives as well as on pyridyl-, pyrimidyl-,

141 The para-selective C-H alkylation of aniline derivatives furnished with a pyrimidine auxiliar

142 ic reactions to produce multiply substituted aniline derivatives in which the position ortho to the n

143 me useful methods to synthesize anilines and aniline derivatives, an important class of compounds thr

144 studies were carried out on both SubPc-TCBD-aniline derivatives, showing the occurrence, in both cas

145 c reactions to generate multiply substituted aniline derivatives.

146 ide range of synthetically useful ortho-OCF3 aniline derivatives.

147 ne geometry interconversion of the resultant aniline-derived enaminones was explored through NMR, FTI

148 ntial genotoxic liability associated with an aniline-derived scaffold in a series of HCV NS5A inhibit

149 Furthermore, when aniline-derived substrates were used, preliminary succes

150 Our optimized procedures enable sequential aniline diazotization/palladium-catalyzed Heck-Matsuda r

151 of the IPU demethylated products; a distinct aniline dioxygenase gene cluster adoQTA1A2BR, which has

152 itu (if desired) to reveal the corresponding anilines directly.

153 ground state moieties are based on dyes with aniline donors--such as Disperse Red 1--whereas the zwit

154 In particular, the vertical OTEDs with aniline-doped PEDOT:PSS films (active area = 1.0 cm(2))

155 s NH-containing compounds, including amides, anilines, enamines, and aliphatic amines, smoothly under

156 cyclo[3.3.1]nonane and a range of amines and anilines ensue under very mild reaction conditions in th

157 pe effects ((13)C-AKIE) and decrease of 4-Cl-aniline fluorescence lifetimes.

158 coupling of o-aminophenols or catechols with aniline functional groups is chemoselective, mild, and r

159 ifficult to prepare by other means of direct aniline functionalizations.

160 In contrast, F12SubPc-TCBD-aniline gave rise to an intense, broad emission, which r

161 ithographic patterning of azidophenol DNA on aniline glass substrates.

162 al analogs of these isoprenols containing an aniline group into isoprenoid diphosphates and protein i

163 quinone intermediates that couple rapidly to aniline groups.

164 m phosphate buffer-based cocktail containing aniline, H2O2, and a G-qudraplex-hemin DNAzyme.

165 The synthesis of sterically hindered anilines has been a significant challenge in organic che

166 ds (e.g., 8-aminoquinoline and 2-(methylthio)aniline), has been investigated.

167 y of substituted anilines, including N-alkyl anilines, has been achived by using cationic [JohnPhosAu

168 wave conditions, a variety of functionalized anilines have been prepared in nearly quantitative yield

169 is a series of primary amines deriving from aniline having been engaged in Zincke reactions.

170 onducted of triazine herbicides, substituted anilines, heterocyclic aromatic amines, and other amines

171 f ligands that promote meta-C-H arylation of anilines, heterocyclic aromatic amines, phenols, and 2-b

172 which is consistent with previous studies on aniline in the gas phase.

173 ify bacteria that incorporated (13)C-labeled aniline in the microcosms established to promote methano

174 phototransformation of four para-substituted anilines in aerated aqueous solutions.

175 epared from arylhydrazine hydrochlorides and anilines in biphasic radical arylation reactions with di

176 te addition of 3-butyn-2-one to a variety of anilines in ethanol is reported.

177 termediates 2-(1H-pyrrolo[2,3-b]pyridin-2-yl)anilines in excellent yields (94-99%) and screened by th

178 nly with the red-shifted absorption tails of anilines in frozen samples (while having a marginal over

179 ifts of 10-15 nm of the absorption maxima of anilines in frozen samples compared to those in liquid a

180 es in the same pot produces meta-substituted anilines in good yields.

181 piperazin-1-yl]-5H-1,2,3-dithiazol-5-ylidene}anilines in high yields (70-92%).

182 Finally, we demonstrate that irradiation of anilines in the presence of a hydrogen peroxide/O2 syste

183 t undergo efficient oxidative couplings with anilines in the presence of periodate as oxidant.

184 eduction of nitroarenes to the corresponding anilines in water.

185 ,6-enynes with a wide variety of substituted anilines, including N-alkyl anilines, has been achived b

186 catalyzes the aerobic oxidation of tertiary anilines, including tetrahydroisoquinolines, to form rea

187 surface area while electropolymerization of aniline increases the number of amino groups (-NH2) for

188 rader as indicated by incorporation of (13)C-aniline into its DNA.

189 ch suggests that anaerobic transformation of aniline is an important process at the site.

190 f 2,3,6,7-tetrabromonaphthalene diimide with aniline is dependent on reaction solvents and additives.

191 e result reveals that the reduction of NB to aniline is through nitrosobenzene to phenylhydroxylamine

192 tion of hetero(aryl) aldehydes and secondary anilines is reported.

193 ic dechlorinations of 2-Cl-, 3-Cl-, and 4-Cl-aniline isomers are each accompanied by distinctly diffe

194 ditions, the free amino functionality of the aniline leads to high ortho:meta regioselectivities, now

195 molecule systems shows that the photoproduct aniline, left unprotonated, serves as a poison for the Q

196 Rearranged phenyl ether- and aniline-linked 2-aminoquinoline derivatives were therefo

197 Aniline loss was observed in nitrate- and sulfate-amende

198 N-acylurea linker bearing an o-amino(methyl)aniline (MeDbz) moiety that enables in a more robust pep

199 Aniline-modified DNA was coupled to catechol-coated elec

200 The ABAO combines an aniline moiety for iminium-based activation of the aldeh

201 A 1,1,4,4-tetracyanobuta-1,3-diene (TCBD)-aniline moiety has been introduced, for the first time,

202 awing ability of the para-substituent on the aniline moiety influences the IEDDA reactivity of the te

203 The installation of the electron-rich aniline moiety was accomplished via a TBSOTf-mediated in

204 ic amides, for which the leaving group is an aniline moiety.

205 An octameric aniline molecule ("octaniline") was incorporated into a

206 plasma stability, GSH adduct formation, and aniline mutagenicity.

207 The nature of the aniline N-capping group is critical for the success of t

208 ties of three different aniline derivatives (aniline, N,N-dimethylaniline, and N,N-diethylaniline) in

209 for more nucleophilic amines such as N-alkyl anilines, N,N-dialkyl amines, and primary aliphatic amin

210 with a CO2-responsive monomer N-(3-amidino)-aniline (NAAN).

211 ice of the electron-withdrawing group on the aniline nitrogen nucleophile, either a cyclopropanation

212 -containing pendants tethered either via the aniline nitrogen or through the carbonyl group containin

213 ramolecular sulfenoamination of alkenes with aniline nucleophiles has been developed.

214 Selected examples of anilines of industrial importance have been prepared in

215 controlled electrochemical polymerization of aniline on gold-coated polycarbonate asymmetric nanochan

216 roduced via in situ electropolymerization of aniline onto a screen-printed graphene support (SPE).

217 which in turn reacted with one equivalent of aniline or a thiole to give thioanilides or a dithioeste

218 1:1 and 2:1 host/guest complexes through the aniline or naphthalene moieties of ANS with cyclodextrin

219 ve hydroaminomethylation of vinylarenes with aniline or nitroarene derivatives in an aqueous microemu

220 and tribrominated acetic acids and also for aniline, phenol, benzene, bromobenzene, chlorobenzene, 1

221 uch as sulfoxides, hydroxylamines, N-oxides, anilines, phenol, an aliphatic amine, and an aliphatic a

222 udy fully rationalized the photochemistry of aniline photocages which is important for the design of

223 w CO2-responsive polymer, poly(N-(3-amidino)-aniline) (PNAAN), coated gold NPs (AuNPs) synthesized by

224 -4-methylaniline to produce the C2-symmetric aniline precursor of the N-heterocyclic carbenoid CuIPhE

225 inium ions formed in situ from aldehydes and anilines predominantly yielded the products of methoxy a

226 er(II)-catalyzed oxidative cross-coupling of anilines, primary alkyl amines, and sodium azide is desc

227 e other hand, the reaction of 2-aminophenols/anilines produced the corresponding benzazine-3-ones or

228 rchloro-1,3-butadiene and electron-deficient anilines producing the Z stereoisomers of a variety of a

229 ose sulfonic acid (AMCell-SO3H), substituted anilines, propenyl-phenols, and phthaldehydic acid.

230 Electron-poor anilines provide superior yields, with electron-rich ani

231 of the nitrogen in nitrogen heterocycles or anilines provides a traceless directing group for subseq

232 roton to the 10-NMe2 group, contrary to the "aniline-pyridine" basicity rule.

233 from HAA by (t)BuO(*) to give functionalized aniline R-NHAr, resulting in a novel amino variant of th

234 hysicochemical properties of both SubPc-TCBD-aniline racemates have been investigated using a wide ra

235 N-(4-Chloro-5H-1,2,3-dithiazol-5-ylidene)anilines react with DABCO in hot PhCl to give N-{4-[N-(2

236 range of commercially available substituted anilines readily participate in this reaction to produce

237 d C-H amination reactions with electron-rich anilines remain an unsolved problem due to catalyst deac

238 generate triarylamines starting from simple anilines, representing an atom-economical preparation of

239 The incorporation of (methylthio)aniline residues into a cage allowed for the design of a

240 g of a highly electron-deficient analogue of aniline results in the formation of soluble electron-def

241 A competition reaction between phenol and aniline revealed condition-dependent selectivity in whic

242 from analysis of a series of 15 substituted anilines reveals that the silver-mediated reaction proce

243 some cases addition of fluorine atoms to the aniline ring allowed for the identification of a novel c

244 ith a fluorine atom at the 3-position of the aniline ring, we generated Ethyl (2-amino-3-fluoro-4-((4

245 esses above the pKa value of the substituted aniline's conjugate acid.

246 Crystals of the protonated aniline salt were analyzed by X-ray diffraction and foun

247 As a matter of fact, H12SubPc-TCBD-aniline showed significant ground-state charge transfer

248 5-diyne-3,4-diyl)bis(N,N-bis(4-methoxyphenyl)aniline) skeleton (1-6) have been synthesized.

249 provide superior yields, with electron-rich anilines sometimes showing competitive Friedel-Crafts al

250 ) and poly[aniline-co-N-(1-one-butyric acid) aniline] (SPAnH) were then incorporated to form an elect

251 N isotope fractionation, while neutral 2-Cl-aniline species shows inverse C and normal N isotope fra

252 e of PAM can thus be adjusted by varying the aniline subcomponent.

253 st binding and specific interactions between aniline subcomponents, allowing a selected one of the th

254 tetrahedral cages, prepared using different aniline subcomponents, which undergo rapid and efficient

255 eleration of the displacement reaction using aniline submonomers in solid-phase peptoid synthesis.

256 uggish reactivity of the weakly nucleophilic aniline submonomers.

257 ap is either 2-anilinopyridinate (ap) or its aniline substituted derivatives.

258 Organic micropollutants containing aniline substructures are susceptible to different light

259 le-crystal X-ray analysis of both SubPc-TCBD-aniline systems showed that each conjugate is a racemic

260 undergoes decomposition to form a protonated aniline (TBAH(+) SbF6 (-) ).

261 also reacted more readily with electron-rich anilines than 2, enabling the design of a system consist

262 reaction is outlined, improving greatly upon aniline, the classical catalyst for imine formation.

263 fluorides fall in the same range as N-bases aniline through pyridine.

264 talysts for the reduction of nitrobenzene to aniline through six sequential photoinduced, proton-coup

265 f unsymmetrically substituted N-methyl/alkyl anilines through a direct three-component coupling react

266 eactions of nitrodiazoesters with a range of anilines through a polar reaction pathway.

267 s, increased from 0.9958+/-0.0013 for 4-OCH3-aniline to 1.0035+/-0.0006 for 4-Cl-aniline, and correla

268 photolytic dechlorination of 2-Cl- and 3-Cl-aniline to aminophenols to obtain insights into the impa

269 reaction at an acidic pH not only encourages aniline to desorb but also increases the probability of

270 The enantioselective addition of anilines to azoalkenes was accomplished through the use

271 electively substituting the meta-position of anilines to produce aromatic phosphonium ions or phospho

272 H amination of cyclohexene using unprotected anilines to provide access to secondary amines in excell

273 Subjecting nosyl protected 2-aryl anilines to this protocol led to meta-C-H arylation at t

274 The excited-state dynamics of an aniline-triazine electron donor-acceptor dyad with an al

275 e spectroscopy results indicate that phenol, aniline, triclosan, and related byproducts are associate

276 ucts of these reactions are valuable because anilines typically require the presence of an electron-w

277 nt knowledge regarding the potential fate of aniline under anaerobic conditions.

278 ssociated with the direct photolysis of 4-Cl-aniline used as a model compound for organic micropollut

279 ) synthesized by oxidative polymerization of aniline using H2O2 generated in-situ from the AOx cataly

280 In contrast, the photolysis of 3-Cl-aniline was almost insensitive to C isotope composition

281 novel triazolopyrimidines wherein the p-SF5-aniline was replaced with substituted 1,2,3,4-tetrahydro

282 s-coupling of aryl tosylates with amines and anilines was achieved by using for the first time a Pd-N

283 acetates featuring indoles and N-substituted anilines was also demonstrated.

284 he presence of Cs(+), whereas those for 3-Cl-aniline were not systematically affected by Cs(+).

285 Two series of easily accessible anilines were identified as inhibitors of influenza A vi

286 Several anilines were identified as providing potent, reversible

287 Electron-rich anilines were observed to displace electron-deficient an

288 primary photoproducts-secondary or tertiary anilines which are not acylated at the nitrogen atom-und

289 ally benign technology for the production of anilines, which are key intermediates for manufacturing

290 dition of ethenesulfonyl fluoride and amines/anilines while the BB monomers were obtained from silyla

291 y dehydrogenative coupling of benzylamine or aniline with diethylsilane, undergo selective silylation

292 a C-X bond annulation of 2-bromo-N-protected aniline with norbornadiene or directing group-assisted r

293 A practical method for radiofluorination of anilines with [(18) F]fluoride via N-arylsydnone interme

294 Anilines with an ortho t-butyl group form atropisomeric

295 e catalyzed cyclization reactions of 2-amino anilines with aryl alkyl ketones under oxidant and metal

296 ative C-C bond formation between unprotected anilines with benzyl alcohols is disclosed.

297 products from simple commercially available anilines with hexafluoroacetylacetone in the presence of

298 his one-step procedure involves treatment of anilines with N-chlorosuccinimide (NCS) and organic base

299 pound lacking the potentially bioactivatable aniline within 8a, but retaining desirable in vitro ADME

300 e the atom-economical use of ammonia to form anilines, without the need for prefunctionalization of t