Synlett 1994; 1994(3): 209-210
DOI: 10.1055/s-1994-22797
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.

The Dianion Carroll Rearrangement - A Cyclic Application

J. F. Genus* , D. D. Peters, J-F. Ding, T. A. Bryson
  • *Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, USA
Further Information

Publication History

Publication Date:
22 March 2002 (online)

Model studies directed towards clerodane insect antifeedants have employed the Carroll reaction to set contiguous stereocenters. Application of dianion chemistry proved to be the most general and highest yielding rearrangement method which generated trans substituted products on cyclic models.

    >