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

Publication details

The article was received on 20 Jul 2011, accepted on 30 Aug 2011 and first published on 31 Aug 2011


Article type: Paper
DOI: 10.1039/C1OB06212C
Citation: Org. Biomol. Chem., 2011,9, 7904-7912
  •   Request permissions

    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

Search articles by author

Spotlight

Advertisements