Tandem Wittig - Reductive annulation decarboxylation approach for the synthesis of indole and 2-substituted indoles

Volvoikar, P.S.; Tilve, S.G.

dc.contributor.author	Volvoikar, P.S.
dc.contributor.author	Tilve, S.G.
dc.date.accessioned	2018-04-27T08:39:06Z
dc.date.available	2018-04-27T08:39:06Z
dc.date.issued	2018
dc.identifier.citation	Tetrahedron Letters. 59(19); 2018; 1851-1854.	en_US
dc.identifier.uri	https://doi.org/10.1016/j.tetlet.2018.04.001
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/5187
dc.description.abstract	A simple tandem Wittig reaction-reductive decarboxylation route is established for the synthesis ofindoles from commercially available o-nitrobenzaldehydes and a stable phosphorane. The method allowsaccess to indoles in a very fast manner without involving any metal or expensive reagents or inert atmo-sphere. Also 2-substituted indoles are obtained which forms an important core of many biological activecompounds.	en_US
dc.publisher	Elsevier	en_US
dc.subject	Chemistry	en_US
dc.title	Tandem Wittig - Reductive annulation decarboxylation approach for the synthesis of indole and 2-substituted indoles	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y