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

Jason E. Camp, Donald Craig, Kiyohiko Funai, Andrew J P White

Research output: Contribution to journalArticle

15 Citations (Scopus)

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.

LanguageEnglish
Pages7904-7912
Number of pages9
JournalOrganic and Biomolecular Chemistry
Volume9
Issue number22
Early online date31 Aug 2011
DOIs
Publication statusPublished - 26 Oct 2011
Externally publishedYes

Fingerprint

alkylidene
Indoles
indoles
Microwaves
acetates
Acetates
reactivity
Derivatives
microwaves
synthesis
products
indoline

Cite this

Camp, Jason E. ; Craig, Donald ; Funai, Kiyohiko ; White, Andrew J P. / Decarboxylative Claisen rearrangement reactions : Synthesis and reactivity of alkylidene-substituted indolines. In: Organic and Biomolecular Chemistry. 2011 ; Vol. 9, No. 22. pp. 7904-7912.
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Decarboxylative Claisen rearrangement reactions : Synthesis and reactivity of alkylidene-substituted indolines. / Camp, Jason E.; Craig, Donald; Funai, Kiyohiko; White, Andrew J P.

In: Organic and Biomolecular Chemistry, Vol. 9, No. 22, 26.10.2011, p. 7904-7912.

Research output: Contribution to journalArticle

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