ライフサイエンスコーパス: aniline

1 nitrosobenzene (NOB), metabolic products of aniline.

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

3 turates the cyclohexene ring en route to the aniline.

4 the phenol could be highly favored over the aniline.

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

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

7 conversion of a racemic alcohol to a chiral aniline.

8 aniline, in acetonitrile, to produce dansyl aniline.

9 producibly create reactions for a variety of anilines.

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

11 ysts for the hydrogenation of nitroarenes to anilines.

12 ized means for preparing aryl fluorides from anilines.

13 hat can further be hydrolyzed to halogenated anilines.

14 rephthalaldehyde and differently substituted anilines.

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

16 with electronically neutral or electron-rich anilines.

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

18 derivatives with expulsion of p-substituted anilines.

19 for the direct substitution of alcohols with anilines.

20 xcellent ortho-selectivities for unprotected anilines.

21 rimination of aromatic primary amines, i.e., anilines.

22 substituted tertiary, secondary, and primary anilines.

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

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

25 agonist (2) propanamides yielded a tertiary aniline (3) with novel SARD activity but poor metabolic

26 ernatively, by using a catalytic quantity of aniline, 3-hydroxyketones can be obtained in high yield

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

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

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

30 rom 4-chloro-N-methyl-N-(2-phenylcyclopropyl)aniline (8) undergoes cyclopropane ring opening with a r

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

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

36 yclization reaction of alpha-keto aldehydes, anilines, activated alkynes, and aromatic nucleophiles i

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

38 tional groups: pyridine, pyrimidine, primary aniline, aldehyde, and ester.

39 Anilines, aliphatic amines, alpha-chiral aliphatic amine

40 ion, while primary and secondary amines, and anilines, all react with high efficiency as the second n

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

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

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

44 rget carboxylic acids (which can bind to the aniline (AN) m-aminobenzenesulfonic acid (MSAN) MIP poly

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

46 reby two PNA probes - functionalized with an aniline and a 1,4-catechol respectively - preferentially

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

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

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

50 nce information was encoded as a sequence of aniline and benzaldehyde subunits linked together by a d

51 benzene oligomers with specific sequences of aniline and benzaldehyde subunits.

52 ubstituted benzyl alcohols, benzylamines and aniline and can also be performed at low temperature for

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

54 were coated by the electropolymerization of aniline and metanilic acid, commingled with target molec

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

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

57 Although aniline and pyridine derivatives interact with His342, b

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

59 nyl-2,5-dimethylpyrrole from one molecule of aniline and three molecules of acetylene activated by KO

60 ared by the self-assembly of di- or tritopic anilines and 2,6-diformylpyridine subcomponents around p

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

62 tions, employing a variety of functionalized anilines and aldehydes suitably poised with Micheal acce

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

64 Various anilines and aromatic as well as aliphatic aldehydes are

65 nthesis of 2,3-disubstituted quinolines from anilines and aromatic or aliphatic epoxides.

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

67 A diverse set of anilines and benzylamines react with different styrenes

68 The broad substrate scope of anilines and benzylic amines and base-promoted condition

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

70 When reactions were performed using anilines and diselenides, the corresponding selenide eth

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

72 access to N-alkylated secondary and tertiary anilines and N-heterocycles.

73 dehydes and a set of four nucleophiles-three anilines and one hydroxylamine-combine through condensat

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

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

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

77 nthetic methods used to generate substituted anilines and quinazolines, both privileged pharmacologic

78 (4)(.)(-)-induced transformation of selected anilines and sulfonamide antibiotics were determined by

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

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

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

82 Further reduction releases N(2)-derived aniline, and the resulting iron species can re-enter the

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

84 les, aryl bromides, ethers, alkyl chlorides, anilines, and a wide range of nitrogen-containing hetero

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

86 reparation of novel fluorinated amino acids, anilines, and aliphatic amines - valuable building block

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

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

89 conimides, accessible from maleic anhydride, anilines, and paraformaldehyde, react with arene diazoni

90 tuted N,N-dimethylvinylamines, p-substituted anilines, and some esters and amides.

91 ctive reaction of either aliphatic amines or anilines are also described, revealing some of the poten

92 ile the innate selectivities for phenols and anilines are approximately 1:4 ortho/para.

93 The use of free cyclic secondary amines and anilines as aminating agents and inexpensive copper acet

94 Using N-hydroxy anilines as electrophiles, which can be easily accessed

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

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

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

98 Our hydrochloric acid/aniline assay revealed that the karyopherin Mtr10 mediat

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

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

101 Aniline-based copolymer, modified with the nanomaterials

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

103 me of the most common arene building blocks (anilines, benzylamines, phenols, benzyl alcohols) and us

104 edicinal chemistry programs as p-substituted aniline bioisosteres.

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

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

107 erene (C(60)) and bis(3,4,5-trimethoxyphenyl)aniline (BTMPA) to the aluminum(III) porphyrin.

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

109 d relates to ethynylation of N-but-3-yn-2-yl-aniline by the ethynide ion.

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

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

112 dical cation quenching (i.e., aniline(*+) -> aniline) by antioxidant moieties present in DOM.

113 Me)C(6)H(4), 2-(TMS-C=C)C(6)H(4)) present on anilines can be appended to the pyrrolo[3,2-b]pyrrole co

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

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

116 of electron-rich derivatives of phenols and anilines, chloroarenes, as well as other haloarenes.

117 thod AlkAniline-Seq (alkaline hydrolysis and aniline cleavage sequencing), TRAC-Seq incorporates smal

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

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

120 00 in N-Methylaniline and by factor of 80 in Aniline compared to the expected values in the case of b

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

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

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

124 Substituted anilines containing a sulfonyl group may be oxidized in

125 nd to significantly promote the oxidation of aniline-containing SAs by Fe(VI) and alter the reaction

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

127 organic compounds-furocoumarin (FC), dansyl aniline (DA), and 7-hydroxycoumarin-3-carboxylic acid (C

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

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

130 ures by sequential coupling of complementary anilines, demonstrating unprecedented control over bond

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

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

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

134 cope (STM) to selectively couple a series of aniline derivatives and create azobenzenes.

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

136 Our studies suggest that unsymmetrical aniline derivatives bearing electron withdrawing groups

137 t a highly para-selective C-H olefination of aniline derivatives by a Pd/S,O-ligand-based catalyst.

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

139 route involves the coupling of 4-substituted aniline derivatives to 2,5-dibromoterephthalonitrile via

140 oduce a range of quinazoline and substituted aniline derivatives using adaptable pH-sensitive cycliza

141 The efficacy of several secondary amines and aniline derivatives was evaluated in the coupling reacti

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

143 ived arenes into the corresponding silylated aniline derivatives, by using a mixture of sodium powder

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

145 inolines employing Michael acceptor-tethered aniline derivatives.

146 uentially activates benzene and N(2) to form aniline derivatives.

147 eaction, affording a variety of alpha-chiral aniline derivatives.

148 a(2) -phosphinines are phosphorus-containing aniline derivatives.

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

150 CO(3) , enabled synthesis of more difficult aniline-derived PDIs.

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

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

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

154 coated with an electrically conducting poly-aniline-emeraldine-salt (PANI-ES) film covered with star

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

156 ss-coupling approach for the construction of anilines, exploiting saturated cyclohexanones as aryl el

157 eaction with indole-2-carboxylic acid and an aniline followed by a Pd-catalyzed cyclization yields te

158 pe ring-opening of N-activated aziridines by anilines followed by Pd-catalyzed annulation with propar

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

160 zed a push-pull molecule named DAF (Dimethyl Aniline Furaldehyde) that possesses a strong positive so

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

162 CDOM* due to radical cation quenching (i.e., aniline(*+) -> aniline) by antioxidant moieties present

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

164 nique alpha-amination approach using various anilines has been developed for arylacetic acids via ada

165 ecting-group-free oxidation of 2-substituted anilines has been developed to generate an electrophilic

166 gement of aryl/alkylidene malononitrile with anilines has been developed with in situ generation of H

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

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

169 rent basicities/nucleophilicities) and three anilines have been measured in both methanol and toluene

170 Anilines have been shown to be especially susceptible to

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

172 2,5-dimethoxyphenyl)-N-[(pyridin-4-yl)methyl]aniline (hereafter referred to as JPIII), a small-molecu

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

174 hydrophobic contacts with a methyl group and aniline in nintedanib and blocks water access to two oxy

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

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

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

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 rresponding beta-keto sulfoxonium ylides and anilines in the presence of TiCl(4) as a Lewis acid (9 e

185 urse of the reaction of dansyl chloride with aniline, in acetonitrile, to produce dansyl aniline.

186 new quinazolines and also highly substituted anilines including cyano derivatives.

187 ,6-enynes with a wide variety of substituted anilines, including N-alkyl anilines, has been achived b

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

189 OM-free solutions, but for two electron-rich anilines, increases in the rate constant were measured.

190 Several chlorophosphite probes and aniline indicators have been evaluated and used for on-t

191 are too acidic result in protonation of the aniline intermediate and results in inhibition of COS/H(

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

193 hydroamination of propargylic alcohols with anilines is described using gold catalysis to give 3-hyd

194 Regioselective ring nitration of N-alkyl anilines is reported using tert-butyl nitrite.

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

196 ndoline with sulfonamides, carboxamides, and anilines is reported.

197 odic acid toward 3,6-dimethoxy-2-(cycloamino)anilines is tunable to give ring-fused benzimidazoles or

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

199 ues featuring phenolic (KGP03 and KGP18) and aniline (KGP05 and KGP156) congeners emerging as lead ag

200 n the cationic indium(I) complex and primary anilines led us to develop an In(I)(+)-catalyzed hydroam

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

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

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

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

205 (4)) reduction of m(7)G sites and subsequent aniline-mediated cleavage of the RNA chain at the result

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

207 The aniline-modified S7 peptide, an UlaG-binding peptide, wa

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

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

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

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

212 Aniline molecules are introduced into the pore structure

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

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

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

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

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

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

219 In addition, the detection of aniline on precoated aluminum-backed thin-layer chromato

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

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

222 1:1 and 2:1 host/guest complexes through the aniline or naphthalene moieties of ANS with cyclodextrin

223 of the copolymer poly(3-amino-benzylamine-co-aniline) (PABA) does not only provide the suitable elect

224 potentials by electro-oxidation of pyrrole, aniline, phenol, or 3,4-ethylenedioxythiophene (EDOT).

225 phene (Th), bithiophene (biTh), and dimethyl aniline (PhNMe(2)), and Au(I)-azide PPh(3)AuN(3) provide

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

227 rin carboxylic acid, furocoumarin and dansyl aniline played a vital role in obtaining a CIE index clo

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

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

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

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

232 to deliver highly functionalized/substituted aniline products or intramolecular ones to furnish carba

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

234 -tetrayl) tetrakis (N,N-bis(4-methoxyphenyl) aniline) (PT-TPA) which can effectively p-dope the surfa

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

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

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

238 Thioethers were formed when anilines reacted with thiols under blue light-emitting-d

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

240 rearrangement and significantly improved the aniline release efficiency.

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

242 CO(2) molecule and the basic amino group of aniline renders enhanced CO(2) separation from O(2) .

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

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

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

246 are not tolerated, and the N-H proton of the aniline ring is responsible for the protonophore activit

247 validate an activation mechanism where the n-aniline ring of fentanyl mediates muOR beta-arrestin thr

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

249 des bromo- and chloro(hetero)arenes, primary anilines, secondary amines, and amide type nucleophiles

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

251 5-diyne-3,4-diyl)bis(N,N-bis(4-methoxyphenyl)aniline) skeleton (1-6) have been synthesized.

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

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

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

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

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

257 uggish reactivity of the weakly nucleophilic aniline submonomers.

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

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

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

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

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

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

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

265 BA-conj-AEMA] and 3-(1-ethyl methacryloylate)aniline to yield hetero-ladder electroconductive hydroge

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

267 The exposure of 2-substituted anilines to PIFA and trifluoroacetic acid or 10 mol % Sc

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

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

270 xygenase enzyme family that commonly convert anilines to their nitroaromatic counterparts.

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

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

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

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

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

276 oredox dual catalytic N-arylation of alkynyl anilines under continuous flow conditions with a subsequ

277 hesizing thioethers and selenide ethers from anilines under solvent-free and transition-metal-free co

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

279 between nitrostyrene and 3-methoxy-dimethyl aniline was modulated in situ by visible light irradiati

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

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

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

283 fluorescent property of the product (dansyl aniline) was used to visually inspect the reaction progr

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

285 Several anilines were identified as providing potent, reversible

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

287 ctionalized amines, aldehydes, and 2-ethynyl anilines were reacted smoothly at ambient temperature to

288 tropic rearrangement reactions of aryl allyl anilines, which deliver exclusively C-H functionalized p

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

290 found to be activated by the interaction of aniline with acetylene, and the barrier associated with

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

292 Selective detection of aniline with probe P2 can be viewed through the naked ey

293 es namely sulfanilic acid, sulfanilamide, or aniline with TPCs in the extract to form an azo dye.

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

295 efficient ortho-C-alkylation of unprotected anilines with a variety of styrenes and alkenes using a

296 Anilines with an ortho t-butyl group form atropisomeric

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

298 borylation can be extended to carbazoles and anilines with excellent ortho selectivity.

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

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