An account of synthetic strategies towards indolocarbazole alkaloids: Arcyriaflavin A and Staurosporinone

Volvoikar, P.S.; Torney, P.S.

dc.contributor.author	Volvoikar, P.S.
dc.contributor.author	Torney, P.S.
dc.date.accessioned	2020-11-17T05:58:25Z
dc.date.available	2020-11-17T05:58:25Z
dc.date.issued	2020
dc.identifier.citation	Tetrahedron. 82; 2020; ArticleID_131756.	en_US
dc.identifier.uri	https://doi.org/10.1016/j.tet.2020.131756
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/6279
dc.description.abstract	An account of synthetic methods developed for indolocarbazole alkaloids arcyriaflavin A and staurosporinone is presented. Based on a common pathway or key intermediate involved, all these methods are broadly grouped into four categories: 1) using bisindolyl maleimide/anhydride, 2) from bisindoles, 3) using Fischer indolisation, 4) involving nitrene insertion. This review discusses in detail the strategies involved in the construction of these two molecules.	en_US
dc.publisher	Elsevier	en_US
dc.subject	Chemistry	en_US
dc.title	An account of synthetic strategies towards indolocarbazole alkaloids: Arcyriaflavin A and Staurosporinone	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y