ライフサイエンスコーパス: carbazole

1 enyl-substituted derivatives of indolo[3,2-b]carbazole.

2 njugated p-(ethynylphenylene), surrounded by carbazole.

3 ubstitution, especially by N-substitution of carbazole.

4 ctive antiangiogenic compound in coal tar is carbazole.

5 ents, diphenylnitrenium ion cyclizes to form carbazole.

6 ton transfer that forms the H-4a tautomer of carbazole.

7 ibenzothiophene approximately dibenzofuran < carbazole.

8 ino-9-methoxy-5, 11-dimethyl-6H-pyrido[4,3-b]carbazole.

9 matization sequence to produce the 2,3-fused carbazole.

10 olecular rearrangements afford phenazine and carbazole.

11 showed various patterns among polybrominated carbazoles.

12 -catalyzed N-arylations and N-alkylations of carbazoles.

13 as compared to those observed in substituted carbazoles.

14 pi orbitals is lower as compared to that of carbazoles.

15 d has the lowest binding constant of all the carbazoles.

16 tituted compounds but into the groove in 2,7 carbazoles.

17 ne-fused benzo[a]carbazoles and indolo[2,3-a]carbazoles.

18 h accepts a broad range of large indoles and carbazoles.

19 Synthesis of indolo[6,7-a]pyrrolo[3,4-c]carbazoles 1, a new class of cyclin D1/CDK4 inhibitors,

20 inhibition by 6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide (Ex-527).

21 4-oxo-3,4-dihydroquinazolin-3-yl)phenyl]- 9H-carbazole-1-carboxamide 6 (BMS-935177) was selected to a

22 (selisistat; 6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide) can suppress HD pathology cause

23 A series of carbazole/1,3,4-oxadiazole hybrid molecules is described

24 -methyl-5-oxo-12H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-12-p ropanenitrile and mitogen-activated prote

25 ,19,21-tetraphenyldiphenanthro[9,10-b:9,10-h]carbazole (15), a very crowded carbazole that exhibits a

26 the expected bianthryl derivative 15 and the carbazole 16, whereas the 9-aminophenanthrene (10), 3-ph

27 Alternatively, carbazole 19 can also be prepared from 1b on reaction wi

28 roduced almost exclusively the corresponding carbazoles 19, 20, and 21, respectively.

29 (9-[3-(cis-3,5-dimethyl-1-piperazinyl)propyl]carbazole, 2), a compound that has been postulated to bi

30 ge transfer (ICT) is observed from the donor carbazole/2,7-dimethoxycarbazole to the acceptor phenyl/

31 An array of carbazoles (23 examples) can be synthesized from substit

32 advancing 3,4-dihydro-9a,4a-(iminoethano)-9H-carbazole 27 to (+)-minfiensine.

33 3-formyl-6-methoxy-carbazole, and 6-methoxy-carbazole-3-methylcarboxylate natural alkaloids.

34 9-Ethyl-N-(3,4,5-trimethoxyphenyl)-carbazole-3-sulfonamide (11a) showed significant antitum

35 A 1,2,3,4-tetrahydro-9a,4a-(iminoethano)-9H-carbazole (4) is a central structural feature of the Str

36 ucopyranosyl)-5H-indolo[2,3-a]pyrrolo[3, 4-c]carbazole-5,7(6H)-dione (NB506), camptothecin-(para)-4be

37 -(3-hydroxypropyl)indeno[2,1-a]pyrrolo[3,4-c]carbazole-5- ones revealed an optimal R9 substitution wi

38 n of the dihydronaphthyl[3,4-a]pyrrolo[3,4-c]carbazole-5-one R(2) and R(12) positions led to the iden

39 ptimized synthetic route to pyrrolo[3,2,1-jk]carbazole (54% overall yield in two steps from indole).

40 With this approach, highly substituted carbazole (6), benzothiophene (10), and quinoline (14) d

41 y-hetarenes, as demonstrated for the hydroxy-carbazole 7 and the hydroxy-benzothiophene 11.

42 onplanar dihydronaphthyl[3,4-a]pyrrolo[3,4-c]carbazole-7-one (8) and corresponding 5,7-dione (7) as p

43 shift, with k(H)/k(D) = 3.4 at 298 K to form carbazole 9 and smaller amounts of two other isocarbazol

44 Azacycloheptatetraene 1f ultimately forms carbazole 9 on the millisecond time scale by the pathway

45 red by cyclomerization reaction of 4,5-bis(6-carbazole-9-yl-hexylsulfanil)phthalonitrile in the prese

46 or seven-membered heteroaromatics (indoles, carbazoles, acridines, and dibenzazepines).

47 Mahanine, a carbazole alkaloid is a potent anticancer molecule.

48 In addition, ancorinazole, an indolo[3,2-a]carbazole also possessing sulfamate and sulfate groups,

49 hat, despite their fused ring structure, the carbazoles also bind in A/T sequences of the DNA minor g

50 Poly[N-9''-heptadecanyl-2,7-carbazole-alt-5,5-(4',7'-di-2-thienyl-2',1',3'-benzot hi

51 n dissociation within the poly(N-decanyl-2,7-carbazole-alt-9,9-dioctylfluorene) (PCzF)/g-C3 N4 PHJ, a

52 This method has also been used to synthesize carbazoles, although a higher reaction temperature is ne

53 atalyzed C-H bond amination reaction to form carbazoles, an important motif that is prevalent in a ra

54 y, we designed and synthesized a fluorescent carbazole analogue of mahanine (alkaloid from Murraya ko

55 The dihydroacridine, phenothiazine, and carbazole analogues were also potent, but nonselective.

56 f annulated thiophene, dibenzothiophene, and carbazoles analogues has been achieved involving alkylat

57 ncipal subunits of carvedilol, including the carbazole and catechol moieties, as well as the linker c

58 Carbazole and derivatives may be useful in the therapy o

59 and six-member benzo-fused heterocycles (9H-carbazole and phenanthridine) when an aromatic amide ani

60 an oxygen molecule, prompts the formation of carbazole and phenoxazine in a facile mechanism.

61 novel series of highly potent and selective carbazole and tetrahydrocarbazole based, reversible inhi

62 Carbazole and trityl substrates with two groups show sat

63 general for N-N dimerization of substituted carbazoles and beta-carbolines, providing entry into sel

64 lly extended to the synthesis of substituted carbazoles and dibenzothiophenes.

65 tructure of the complexes formed between the carbazoles and DNA.

66 corresponding 3-pyrrolin-2-one-fused benzo[a]carbazoles and indolo[2,3-a]carbazoles.

67 pper catalyst, nitrogen nucleophiles such as carbazoles and primary amides undergo C-N coupling with

68 he complexes formed between the 3,6- and 2,7-carbazoles and the self-complementary oligomer d(GCGAATT

69 azole was one of the most active halogenated carbazoles and, like TCDD, contains 4 lateral substituen

70 synthesis of glycozoline, 3-formyl-6-methoxy-carbazole, and 6-methoxy-carbazole-3-methylcarboxylate n

71 pentachlorobiphenyl (PCB-126), indolo[3,2-b]-carbazole, and beta-naphthoflavone.

72 dihydroacridine, phenoxazine, phenothiazine, carbazole, and diphenylamine analogues were synthesized

73 ls, such as indole-3-carbinol, indolo[3, 2-b]carbazole, and UV photoproducts of tryptophan (TRP), hav

74 useful precursors of cyanocyclopentadienes, carbazoles, and aza-analogues.

75 uding naphtols, phenols, pyridines, indoles, carbazoles, and thiophenes in combination with amines an

76 ctral shift data for 11 relevant halogenated carbazoles are reported, along with their gas chromatogr

77 750 to 950 degrees C gives pyrrolo[3,2,1-jk]carbazole as the major product.

78 The reaction could also be carried out using carbazoles as sensitizers, and quantitative yields could

79 safer and more specific than the traditional carbazole assay.

80 loped to prepare suitably substituted stable carbazoles B1-B3, G1-G3, and R1-R3.

81 Two benzoylpyridine-carbazole based fluorescence materials DCBPy and DTCBPy,

82 A new class of highly fluorescent and stable carbazole-based dendrimers (1-5) that contain the ethyny

83 In the present study, carbazole-based diaza[6]helicenes were synthesized utili

84 ure the rates of regeneration of six organic carbazole-based dyes by nine ferrocene derivatives whose

85 porous fibers fabricated by self-assembly of carbazole-based macrocyclic molecules.

86 vided higher regioselectivity in the case of carbazole-based substrates.

87 A new carbazole-based tetraimidazole ligand 1,3,6,8-tetra(1H-i

88 5',5',5',4',4'-pentafluoro-1',3'-dioxopentyl)carbazole (bdc), was synthesized to efficiently excite e

89 ificity and that the 2,7 and 3,6 substituted carbazoles bind to the minor groove in opposite orientat

90 g results indicate a broad AT specificity of carbazole binding and a pattern in agreement with a mino

91 face plasmon resonance biosensor analysis of carbazole binding to an oligomer with an AATT central se

92 The 3,6-carbazole binds approximately twice as strongly to the G

93 The surprising result is that the 2,7 carbazole binds in AT sequences with hydrogen bonds invo

94 thermal stability attributable to the rigid carbazole building block.

95 otocol for the preparation of a series of 9H-carbazoles by photostimulated SRN1 substitution reaction

96 (C18H13Cl11), and a novel mixed chloro/bromo-carbazole (C12H5NCl2Br2) in a number of sediments analyz

97 N-H carbazoles can be produced from 2-chloroanilines and ary

98 ese results, it is clear that the fused ring carbazoles can bind strongly in the DNA minor groove wit

99 The P7C3 class of aminopropyl carbazole chemicals fosters the survival of neurons in a

100 ions to construct models of the minor-groove-carbazole complexes and to draw conclusions regarding th

101 Structural analysis of carbazole complexes with an AATT sequence by 2D NMR meth

102 The 3,6-carbazole compound binds in a more "classical" model tha

103 An arylated-carbazole conjugated polymer with a deep HOMO level has

104 gn and syntheses of four novel benzimidazole-carbazole conjugates and demonstrate their high binding

105 les, while the others were mixed halogenated carbazoles containing, in addition to bromine, either ch

106 The carbazole-containing molecule TAM4 after oxidation under

107 environment as a result of the production of carbazole-containing polymers present in a wide variety

108 semiconductors (HTPS), which are based on a carbazole core and the oxiran and thiiran reactive group

109 The indolo[3,2-b]carbazole core has a larger resonance structure that inc

110 allel strategies were exploited to forge the carbazole core: 6pi-electrocyclization/aromatization and

111 pounds (including pharmacologically relevant carbazoles, delta-lactams, and oxindole derivatives).

112 pplied to synthesize the core of a bioactive carbazole derivative in a concise manner.

113 uced electron-transfer (PET) mechanism using carbazole derivatives as the photosensitizer.

114 reactions toward a series of polyphenylated carbazole derivatives differing in their N-substitution

115 Specifically, cyclization to form carbazole derivatives occurs negligibly, if at all, with

116 tuents and the core moiety, the indolo[3,2-b]carbazole derivatives studied all have a weaker coupling

117 nishes highly substituted and functionalized carbazole derivatives via a double annulation process th

118 , based on conjugates of aminoadamantane and carbazole derivatives was synthesized and investigated.

119 vel substrates: trityl (triphenylmethyl) and carbazole derivatives.

120 o that of the previously reported dicationic carbazole derivatives.

121 Synthesized carbazole derived with fluorophore compound 12 was disco

122 oach, we tested anti-trypanosomal effects of carbazole-derived compounds called "Curaxins".

123 Ancorinazole is the first indolo[3,2-a]carbazole described as a natural product.

124 Among these was an aminopropyl carbazole, designated P7C3, endowed with favorable pharm

125 nthetic and natural product-based tricyclic (carbazole, dibenzo[b,d]furan, and dibenzo[b,d]thiophene)

126 Introduction of planarized fluorene, carbazole, dibenzo[b,d]thiophene or dibenzo[b,d]thiophen

127 with core units comprising dibenzothiophene, carbazole, dibenzofuran and fluorene.

128 Substituted carbazoles, dibenzofurans, and tricyclic compounds conta

129 cellent separation (by LC and GC methods) of carbazole, dibenzothiophene, fluorenones, xanthones, and

130 Carbazole dications have shown excellent activity agains

131 sequence-dependent DNA binding properties of carbazole dications.

132 t are quite different for the 2,7 NH and NMe carbazole dications.

133 ated indole rings leading to carbazolo[2,3-b]carbazole diimides (CbDIs) with exclusive syn-connectivi

134 (BMVC, 3, 6-bis-(1-methyl-4-vinylpyridinium)-carbazole diiodide) and duplex-binding fluorophores (Hoe

135 s for the effects of substituent position on carbazole-DNA affinities.

136 minor groove and we proposed models for the carbazole-DNA complexes with the carbazole nitrogen faci

137 w electron-accepting units and di(tert-butyl)carbazole (DTC) as the electron-donating units.

138 n (aromatization) of this to give the target carbazole (e.g. 4).

139 or cyclization of the aminoethyl moiety to a carbazole (e.g., 34, 36) or beta-carboline (i.e., 37), r

140 methyl-5-oxo-5H-indolo(2,3-a)py rrolo(3,4-c)-carbazole], enhanced basal and agonist-stimulated phosph

141 oxyphenyl)-6-pentyl-5,11-dihydroindolo[3,2-b]carbazole exceed 10(-3) cm(2)/V.s at high electric field

142 Some halogenated carbazoles exhibit characteristics of persistent organic

143 he high-affinity ligand 6-formylindolo[3,2-b]carbazole (FICZ) determines a boost in degranulation.

144 Here we report that 6-formylindolo[3,2-b]carbazole (FICZ), a tryptophan photoproduct and endogeno

145 tryptophan photoproduct 6-formylindolo[3,2-b]carbazole (FICZ), an aryl hydrocarbon receptor ligand, h

146 ered systemic levels of 6-formylindolo[3,2-b]carbazole (FICZ), an enigmatic endogenous ligand for the

147 onists including TCDD, 6-formylindolo-[3,2-b]carbazole (FICZ), and 3-3'-diindolylmethane (DIM) and th

148 arbon receptor agonist 6-formylindolo[3,2-b] carbazole (FICZ), is a UVB photoproduct of tryptophan an

149 endogenous AhR ligand, 6-formylindolo(3,2-b)carbazole (FICZ), on the differentiation and functions o

150 oproduct and AhR ligand 6-formylindolo[3,2-b]carbazole (FICZ).

151 re a palladium-catalyzed construction of the carbazole framework and an annulation of the pyran ring,

152 aped (LXL)Au(I)-pincer complexes, based on a carbazole framework flanked by two mesoionic carbenes (M

153 al and efficient synthesis of 4,9-dihydro-1H-carbazoles from 3-allenylmethylindoles is reported.

154 es the mild and stereoselective formation of carbazoles from biaryl azides.

155 The synthesis of a series of substituted carbazoles from the corresponding 2-nitrobiphenyl deriva

156 overning the formation of benzimidazoles and carbazoles from the reaction of N-(biphenyl)pyridin-2-am

157 fonium salt of a carbamato borate based on a carbazole function, its establishment as a PhLAG, and th

158 The indolo[2,3-a]carbazole glycosides are potent antitumor antibiotics cu

159 methyl-5-oxo-5H-indolo(2,3-a)pyr rolo(3,4-c)-carbazole (Go 6976), a specific inhibitor of Ca(2+)-depe

160 methyl-5-oxo-5H-indolo(2,3-a)pyrrolo(3, 4-c)-carbazole (Go 6976), an inhibitor of calcium-dependent P

161 methyl-5-oxo-5H-indolo[2,3-a]py rrolo[3,4-c] carbazole], Go6983 [2-[1-(3-dimethylaminopropyl)-5-metho

162 se of strong electron-donating properties of carbazole group.

163 N-Substituted carbazole has also been prepared by following this metho

164 positions octa-substituted with alkyl linked carbazole has been prepared by cyclomerization reaction

165 ctrophilic chloroquinoline and electron-rich carbazole has opened up new opportunities.

166 Pd(II)-catalyzed direct synthesis of benzo[a]carbazoles has been achieved through aminopalladation of

167 ent one-pot protocol for the synthesis of NH-carbazoles has been described.

168 sis of aryl and heteroaryl-annulated cyclo[b]carbazoles has been developed via SnCl4-mediated one-pot

169 The carbazoles have been shown to arise directly from the co

170 The first substituted pyrrolo[3,2,1-jk]carbazoles have been synthesized by FVP methods and also

171 ported the discovery of P7C3, an aminopropyl carbazole having proneurogenic and neuroprotective prope

172 ported the discovery of P7C3, an aminopropyl carbazole having proneurogenic and neuroprotective prope

173 noid ring in fused polycyclic heteroaromatic carbazole (i.e., [2,3]-benzoindole) skeletons.

174 environmental contaminant, and indolo(3,2-b)carbazole (ICZ), a metabolite of a natural pesticide fou

175 ther, administration of 6-formylindolo[3,2-b]carbazole in vivo enhances NK cell control of tumors in

176 icipated highly substituted naphthalenes and carbazoles in good to excellent yields.

177 provides 3,4-dihydro-9a,4a-(iminoethano)-9H-carbazoles in high enantiomeric purity.

178 also supported a minor groove complex of the carbazoles in orientations in agreement with the previou

179 tudy discovering the seven mixed halogenated carbazoles in the environment.

180 resulting in the direct synthesis of benzo[a]carbazoles in which a wide variation of substituents at

181 onding C-N coupled products, N-R-substituted carbazoles, in 82-98% yield.

182 d can be used in the synthesis of a range of carbazoles, including the natural products Clausine P an

183 twisted 89 degrees from the plane of central carbazole, indicating a lack of electron delocalization

184 Substituted carbazoles, indoles, and dibenzofurans are readily prepa

185 In addition to antiangiogenic activity, carbazole inhibited the production of inflammatory IL-15

186 on by the agonist FICZ (6-formylindolo[3,2-b]carbazole) inhibited NMuMG migration, whereas the antago

187 on series of potent and selective reversible carbazole inhibitors of BTK.

188 hand, AHR activation by 6-formylindolo[3,2-b]carbazole interfered with T(reg) cell development, boost

189 angiogenic and anti-inflammatory activities, carbazole is likely a major component of the antipsoriat

190 flexible approach to 3-pyrrolin-2-one fused carbazoles is disclosed.

191 s to 6-arylbenzimidazoles and N-pyridinyl-9H-carbazoles is presented.

192 new method for the assembly of unsymmetrical carbazoles is reported.

193 yl)-10,15-dihydro-5H-diindolo[3,2-a:3', 2'-c]carbazole (KR131) with compositive perovskite absorber.

194 1,3,6,8-tetra(1H-imidazol-1-yl)-9-methyl-9H-carbazole (L) has been synthesized.

195 lization of the 3,6-bis-styryl derivative of carbazole leading to sterically less demanding aza[7]hel

196 easing heteroaromaticity (dibenzothiophene < carbazole < dibenzofuran).

197 ted here to the possibility that halogenated carbazoles may currently be emitted into the environment

198 conjugated cyclic motifs are presented with carbazole moieties as donors and borane moieties as acce

199 -5 consists of rigid, aromatic porphyrin and carbazole moieties as well as linear ethynylene linkers,

200 The purpose of combining of carbazole moieties with phthalocyanine on the peripheral

201 a carbaldehyde or malononitrile group on the carbazole moiety is found to quench fluorescence severel

202 ction of 2,7-dimethoxy substituents onto the carbazole moiety lowers the value of E(S), although E(T)

203 We have identified an amino-alcohol carbazole (N-CBZ) as a PfHsp90-selective inhibitor by vi

204 To test and refine the models, carbazole-N-methyl substituted derivatives have been syn

205 This aminopropyl carbazole, named P7C3, is orally bioavailable, crosses t

206 h imidazoline groups for H-bonding while the carbazole NH points out of the minor groove.

207 onds involving one imidazoline group and the carbazole NH.

208 els for the carbazole-DNA complexes with the carbazole nitrogen facing out of the groove for 3,6 subs

209 to diphenylamino substituted derivatives of carbazole, no effect of the position of methoxy groups o

210 on is possible via ligation of a cyano-vinyl carbazole nucleoside with an opposite thymine when irrad

211 t; thus, a change from NH- to N-decyl on the carbazole nucleus was carried out.

212 The effect of carbazole on upstream pathways in human psoriasis was de

213 ate substitution methodologies on the parent carbazole or by palladium-catalyzed cyclization of di-(p

214 The molecular arms are based on a carbazole or oligo(phenylene ethynylene) core with a str

215 Other dietary factors such as carbazoles or tryptophan-enriched proteins have anti-inf

216 phene S,S-dioxide and the donor is fluorene, carbazole, or arylamine.

217 -methyl-5-oxo-5H-indolo[2,3-a]pyrrolo[3 ,4-c]carbazole] or PKC-alpha short hairpin RNA.

218 The abundance of mixed halogenated carbazoles peaked at depths of 12-16 cm, remained at rel

219 ures for a total of 15 novel polyhalogenated carbazoles (PHCs) with the general molecular formula C12

220 Polyhalogenated carbazoles (PHCZs) have been increasingly detected in th

221 veral other nitrogen heterocycles, including carbazole, phenothiazines, and tetrahydroquinoline.

222 and the experimental profiles of chlorinated carbazole, phenoxazine, and phenazine suggests the forma

223 the three nitrogenated dioxin-like species, carbazole, phenoxazine, and phenazine via unimolecular r

224 Carbazoles possessing complex molecular architecture can

225 tryptophan derivative, 6-formylindolo[3,2-b]carbazole, potentiates NK cell IFN-gamma production and

226 similar or different) substrates from acetyl carbazole proceeds via a stepwise pathway.

227 The substitution pattern of the carbazole product can be controlled by the design of the

228 under extremely mild conditions and produces carbazole products in good to excellent yields.

229 broad range of functional groups, and yield carbazole products in the absence of unwanted side produ

230 P7C3 aminopropyl carbazoles promote neuronal survival by enhancing nicoti

231 aining an electroactive polymer, polyvinyl-N-carbazole (PVK) (97 wt %), and single-walled carbon nano

232 n-relay mechanism: the transiently generated carbazole radical cation acts as an oxidant to return th

233 C3-substituted indoles and carbazoles react with alpha-aryl-alpha-diazoesters under

234 ryl hydrocarbon-receptor ligand indolo[3,2-b]carbazole resulted in a concentration-dependent increase

235 9-[3-(cis-3,5-Dimethyl-1-piperazinyl)propyl]carbazole (rimcazole) has been characterized as a sigma

236 he position of the two amidine groups on the carbazole ring influences significantly the drug-DNA int

237 lization of di-(p-tolyl)amine to provide the carbazole ring system.

238 Analogues in which the carbazole ring was replaced with a freely rotating diphe

239 are formed by an electron donor moiety, the carbazole ring, and an electron acceptor moiety, the pol

240 mately 90 degrees between the phenyl and the carbazole rings due to steric interactions.

241 ]thiophene > dibenzo[b,d]furan > 9-methyl-9H-carbazole series.

242 Application of these methods to carbazoles substituted at either the 3,6 or 2,7 position

243 upon self-assembly of a monolayer of t-butyl carbazole-substituted phosphonic acid molecules and subs

244 ass of calixpyrrole analogue, containing two carbazole subunits in lieu of two of the four acetone br

245 Carbazole sulfonamides are a novel promising class of an

246 Two series of carbazole sulfonamides related to Combretastatin A4 (1)

247 heterocycles, such as indoles, pyrazole, and carbazole, sulfonamides, as well as electron-deficient a

248 acids, and other oxygen-containing species, carbazoles, sulfones, and thiophenes from small crude oi

249 itutes the first example of a multicomponent carbazole synthesis.

250 nd strong donors in the arms (diarylamine or carbazole), TAM1-TAM3 exhibit large solvatochromic effec

251 Precursor carbazole terminated dendrons and dendrimers up to gener

252 9,10-b:9,10-h]carbazole (15), a very crowded carbazole that exhibits an 81 degree end-to-end twist bu

253 We have found that any carbazole that is not substituted in the 1,3,6,8 positio

254 sized with fused aromatic ring systems (e.g. carbazoles) that do not resemble the classical paradigm

255 oduce valuable fused 5,7-dihydroindolo[2,3-b]carbazoles through the functionalization of two indole C

256 .g., N,N-dimethylaniline, diphenylamine, and carbazole) through an initial one-electron transfer.

257 The carbazoles thus form a new type of DNA minor groove comp

258 ide array of indoles, as well as pyrrole and carbazole, to afford the corresponding N-alkylation prod

259 Carbazole treatment also reduced activity of inducible n

260 Recognition properties of the novel bis(carbazole) tris-ureidic-based receptors 1 and 2 toward d

261 The redox properties of the carbazole unit can thus be rationally tuned to improve c

262 vealed that copolymerizing electron-donating carbazole unit into the poly(9,9-dioctylfluorene) backbo

263 ation functionalization via substituting the carbazole unit provides a platform for the synthesis of

264 tion rate and the reduction potential of the carbazole unit tethered to the aminocatalyst.

265 chemical structure featuring a disubstituted carbazole unit, five stereogenic centres-three of which

266 The carbazole unit, however, is also involved in another ste

267 hiral amine catalyst, bearing a redox-active carbazole unit, which could rapidly reduce the highly re

268 surroundings and the electronics of the core carbazole unit.

269 alized via electrophilic substitution on the carbazole unit.

270 system carrying halogen substituents at the carbazole units.

271 These precatalysts produce N-substituted carbazoles upon activation, which cannot consume startin

272 PHCZs were analyzed along with unsubstituted carbazole using gas chromatography coupled with single-

273 entially converted into a highly substituted carbazole via a retro-4pi/6pi-electrocyclization-N-acyla

274 for the synthesis of a series of chlorinated carbazoles via the Cadogan cyclization is also demonstra

275 Carbazole was found to inhibit rac activation as a mecha

276 hways in human psoriasis was determined, and carbazole was shown to inhibit signal transducer and act

277 on responses for the most active halogenated carbazoles was similar to that observed for 2,3,7,8-tetr

278 sive MDA-MB-468 breast cancer cells by these carbazoles was similar to that observed for other dioxin

279 s of three derivatives of 1,8-di(pyrid-2'-yl)carbazole were prepared by Stille-type coupling of 2-(tr

280 The carbazoles were prepared by appropriate substitution met

281 ubstituted pyrazoles, pyrroles, indoles, and carbazoles were screened to identify potential inhibitor

282 A series of thienylphenothiazine decorated carbazoles were synthesized and characterized by optical

283 Substituted 9H-carbazoles were synthesized in low to excellent yields (

284 ere tentatively identified as polybrominated carbazoles, while the others were mixed halogenated carb

285 e photoinduced, copper-catalyzed coupling of carbazole with alkyl bromides.

286 erization of new derivatives of indolo[3,2-b]carbazole with differently substituted phenyl groups at

287 )-P7C3-S243 is a neuroprotective aminopropyl carbazole with improved druglike properties compared wit

288 this approach is not limited to reactions of carbazoles with iodobenzene and alkyl halides.