Pyrrolocarbazole and dipyrrolocarbazoles have been synthesized via the Hemetsberger indole synthesis, starting from 9-ethyl carbazole-3-carbaldehyde and 9-ethylcarbazole-3,6-dicarbaldeyde, respectively. The pyrrolocarbazole structures were confirmed through H-1 NMR, C-13 NMR, IR, mass spectrometry and single crystal X-ray diffraction techniques. The targeted compounds showed potent in vitro cytotoxicity against human colon cancer HT29 cells.TUBITAKTurkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [113Z159]This work was funded by TUBITAK grant 113Z159 to E.A., I.F.S., and H.K. We thank the NMR facility of Gebze Technical University
The final examples in our ellipticine/pyrrolocarbazole synthesis programme are 7,10-dimethoxyellipti...
International audiencePyrrolo[2,3-a]carbazole-3-carbaldehydes are potent Pim kinase inhibitors with ...
A simple and flexible approach to 3-pyrrolin-2-one fused carbazoles is disclosed. The key step invol...
A number of novel pyrrolo[3,2-c]carbazole-2-carbohydrazides 5a–d was prepared from readily available...
A number of novel pyrrolo[3,2-c]carbazole-2-carbohydrazides 5a–d was prepared from readily available...
The unexpected result for the formylation of N-ethylcarbazole under the Vilsmeier-Haack conditions (...
In the course of structure–activity relationship studies on granulatimide analogues, new pyrrolo[3,4...
International audienceThe synthesis of new pyrrolocarbazoles substituted at N-1/N-10 positions is de...
The syntheses of dipyrrolo[3,4-a:3,4-c]carbazole-1,4,6-triones and dipyrrolo[3,4-a:3,4-c]carbazole-3...
International audienceThe synthesis of new pyrrolo[2,3-a]carbazole derivatives diversely substituted...
<p>The unexpected result for the formylation of <i>N</i>-ethylcarbazole under the Vilsmeier–Haack co...
The synthesis of (6-ethyl-1,6-dihydropyrrolo[3,2-c]carbazol-2-yl)methanol 5 and (6-ethyl-6,11-dihydr...
Department of Chemistry, Bose Institute, 93/1, Acharya Prafulla Chandra Road, Calcutta-700 009 Manu...
International audienceThe carbazole framework is found in many natural compounds of biological inter...
The synthesis of substituted pyrrolo[3,4-a]carbazole-1,3-diones, pyrrolo[3,4-c]carbazole-1,3-diones,...
The final examples in our ellipticine/pyrrolocarbazole synthesis programme are 7,10-dimethoxyellipti...
International audiencePyrrolo[2,3-a]carbazole-3-carbaldehydes are potent Pim kinase inhibitors with ...
A simple and flexible approach to 3-pyrrolin-2-one fused carbazoles is disclosed. The key step invol...
A number of novel pyrrolo[3,2-c]carbazole-2-carbohydrazides 5a–d was prepared from readily available...
A number of novel pyrrolo[3,2-c]carbazole-2-carbohydrazides 5a–d was prepared from readily available...
The unexpected result for the formylation of N-ethylcarbazole under the Vilsmeier-Haack conditions (...
In the course of structure–activity relationship studies on granulatimide analogues, new pyrrolo[3,4...
International audienceThe synthesis of new pyrrolocarbazoles substituted at N-1/N-10 positions is de...
The syntheses of dipyrrolo[3,4-a:3,4-c]carbazole-1,4,6-triones and dipyrrolo[3,4-a:3,4-c]carbazole-3...
International audienceThe synthesis of new pyrrolo[2,3-a]carbazole derivatives diversely substituted...
<p>The unexpected result for the formylation of <i>N</i>-ethylcarbazole under the Vilsmeier–Haack co...
The synthesis of (6-ethyl-1,6-dihydropyrrolo[3,2-c]carbazol-2-yl)methanol 5 and (6-ethyl-6,11-dihydr...
Department of Chemistry, Bose Institute, 93/1, Acharya Prafulla Chandra Road, Calcutta-700 009 Manu...
International audienceThe carbazole framework is found in many natural compounds of biological inter...
The synthesis of substituted pyrrolo[3,4-a]carbazole-1,3-diones, pyrrolo[3,4-c]carbazole-1,3-diones,...
The final examples in our ellipticine/pyrrolocarbazole synthesis programme are 7,10-dimethoxyellipti...
International audiencePyrrolo[2,3-a]carbazole-3-carbaldehydes are potent Pim kinase inhibitors with ...
A simple and flexible approach to 3-pyrrolin-2-one fused carbazoles is disclosed. The key step invol...