Molecular Iodine assisted electrocyclisation: Synthesis of Arcyriaflavin A and formal synthesis of Staurosporinone

Torney, P.S.; Shirsat, R.N.; Tilve, S.G.

dc.contributor.author	Torney, P.S.
dc.contributor.author	Shirsat, R.N.
dc.contributor.author	Tilve, S.G.
dc.date.accessioned	2015-06-04T04:29:05Z
dc.date.available	2015-06-04T04:29:05Z
dc.date.issued	2014
dc.identifier.citation	Synlett. 25(15); 2014; 2121-2126.	en_US
dc.identifier.uri	http://dx.doi.org/10.1055/s-0034-1378536
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/3074
dc.description.abstract	A new method for the synthesis of the indolocarbazole alkaloid arcyriaflavin A is described. The synthetic strategy employs a graphite-catalysed alkenation, one-pot oxidation-Wittig reaction, iodine-catalysed electrocyclisation and nitrene insertion as the key steps. The strategy also constitutes a formal synthesis of another indolocarbazole alkaloid staurosporinone.	en_US
dc.publisher	Thieme Publishing	en_US
dc.subject	Chemistry	en_US
dc.title	Molecular Iodine assisted electrocyclisation: Synthesis of Arcyriaflavin A and formal synthesis of Staurosporinone	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y