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Lewis acid catalyzed C-3 alkylidenecyclopentenylation of indoles: an easy access to functionalized indoles and bisindoles†
Praveen Prakash,P. Sasikumar,P. Preethanuj,Florian Jaroschik,Dominique Harakat,Jean-Luc Vasse
RSC Advances Pub Date : 03/16/2015 00:00:00 , DOI:10.1039/C5RA01107H
Abstract

A Lewis acid catalyzed C-3 alkylidenecylopentenylation of indoles through the ring opening of pentafulvene derived diazabicyclic olefins has been developed. The present protocol offers an efficient route toward the synthesis of indole and bisindole derivatives. The role of the hydrazine group, as a reaction carrier in the strategy has also been demonstrated by the stepwise synthesis of functionalized bisindole.

Graphical abstract: Lewis acid catalyzed C-3 alkylidenecyclopentenylation of indoles: an easy access to functionalized indoles and bisindoles
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