Skip to main navigation Skip to search Skip to main content

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

  • Jason E. Camp
  • , Donald Craig
  • , Kiyohiko Funai
  • , Andrew J. P. White
  • Imperial College London
  • University of Nottingham

Research output: Contribution to journalArticlepeer-review

19   Link opens in a new tab Citations (SciVal)

Abstract

Microwave-assisted decarboxylative Claisen rearrangement (dCr) reactions of substituted acetate derivs. of 3-(hydroxyalkyl)indoles give de-aromatized products. The reactivity of the resultant compds. was evaluated. [on SciFinder(R)]
Original languageEnglish
Pages (from-to)7904-7912
Number of pages9
JournalOrganic and Biomolecular Chemistry
Volume9
Issue number22
DOIs
Publication statusPublished - 31 Aug 2011

Bibliographical note

M1 - Copyright (C) 2018 American Chemical Society (ACS). All Rights Reserved.

CAPLUS AN 2011:1370378(Journal; Online Computer File)

Keywords

  • decarboxylative Claisen rearrangement hydroxyalkyl indole acetate
  • crystal mol structure methyl tosyl tosylethylidene indoline

Fingerprint

Dive into the research topics of 'Decarboxylative Claisen rearrangement reactions: synthesis and reactivity of alkylidene-substituted indolines.'. Together they form a unique fingerprint.

Cite this