Download PDF
Synlett 1993; 1993(4): 281-282
DOI: 10.1055/s-1993-22432
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

A New Synthesis of Indoles Involving a Tandem Sigmatropic Rearrangement/Michael Addition Sequence

Matthew Gray* , Philip J. Parsons, Adrian P. Neary
  • *Department of Chemistry, University of Reading, Whiteknights, P.O. Box 224, Reading, Berkshire RG6 2AD, England
Further Information

Publication History

Publication Date:
19 March 2002 (online)

  PDF Download  Permissions and Reprints All articles of this category

A general route to substituted indoles (3) starting from 2-amido-phenyl ketones and aldehydes (1), utilising a tandem 2,3-sigmatropic rearrangement/Michael addition sequence is reported.