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Synthesis of thienocarbazoles by reductive cyclization of 6-(2’- nitrophenyl)benzo[b]thiophenes

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Thienocarbazoles are bioisosters of anti-tumoural pyridocarbazoles, ellipticine and olivacine. Methylated thienocarbazoles 1 were synthesized by reductive cyclization of 6-(2'nitrophenyl) benzo[b]thiophenes 2, using triethylphosphite. Compounds 2 were obtained by palladium-catalyzed cross-coupling between 2-bromo or iodonitrobenzenes and 6-boronic esters of methylated benzo[b]thiophenes (communication presented at this meeting).

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Ferreira, Isabel C.F.R.; Queiroz, Maria-João R.P.; Kirsch, Gilbert (2000) – Synthesis of thienocarbazoles by reductive cyclization of 6-(2’- nitrophenyl)benzo[b]thiophenes. In XIX th European Colloquium on Heterocyclic Chemistry. Aveiro

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