Jump to main content
Jump to site search

Issue 22, 2011
Previous Article Next Article

Decarboxylative Claisen rearrangement reactions: synthesis and reactivity of alkylidene-substituted indolines

Author affiliations

Abstract

Microwave-assisted decarboxylative Claisen rearrangement (dCr) reactions of substituted acetate derivatives of 3-(hydroxyalkyl)indoles give de-aromatised products. The reactivity of the resultant compounds was evaluated.

Graphical abstract: Decarboxylative Claisen rearrangement reactions: synthesis and reactivity of alkylidene-substituted indolines

Back to tab navigation

Supplementary files

Article information


Submitted
20 Jul 2011
Accepted
30 Aug 2011
First published
31 Aug 2011

Org. Biomol. Chem., 2011,9, 7904-7912
Article type
Paper

Decarboxylative Claisen rearrangement reactions: synthesis and reactivity of alkylidene-substituted indolines

J. E. Camp, D. Craig, K. Funai and A. J. P. White, Org. Biomol. Chem., 2011, 9, 7904
DOI: 10.1039/C1OB06212C

Social activity

Search articles by author

Spotlight

Advertisements