Construction of Hexahydropyrido[3,2-c]carbazole and Hexahydropyrrolo[3,2-c]carbazole Skeletons for the Synthesis of Related Indole Alkaloids

dc.contributor.authorHızlıateş C.G.
dc.contributor.authorGülle S.
dc.date.accessioned2025-04-10T11:09:08Z
dc.date.available2025-04-10T11:09:08Z
dc.date.issued2016
dc.description.abstractSynthesis of tetracyclic hexahydropyrido[3,2-c]carbazoles (9a and 9b) and hexahydropyrrolo[3,2-c]carbazoles (13a and 13b) structures was achieved via a new synthetic approach for the synthesis of related indole alkaloids such as deethylaspidospermidine and deethylibophyllidine. Hexahydropyrrolo[3,2-c]carbazole structure was constructed for the first time starting from ethyl 4-oxo-cyclohexanecarboxylate in seven steps. Some tetrahydrocarbazole derivatives (4, 5, 6, 7, 11, and 12) were also synthesized. © 2015 HeteroCorporation
dc.identifier.DOI-ID10.1002/jhet.2467
dc.identifier.urihttp://hdl.handle.net/20.500.14701/48502
dc.publisherHeteroCorporation
dc.titleConstruction of Hexahydropyrido[3,2-c]carbazole and Hexahydropyrrolo[3,2-c]carbazole Skeletons for the Synthesis of Related Indole Alkaloids
dc.typeArticle

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