Download PDF
Synlett 1996; 1996(12): 1162-1164
DOI: 10.1055/s-1996-5718
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.

Novel Application of the Intramolecular Prins Reaction: (-)-Anisatin Model Study

Jeffrey A. Charonnat* , Nobuko Nishimura, Bruce W. Travers, Jack R. Waas
  • *Department of Chemistry, California State University, Northridge, 18111 Nordhoff Street, Northridge, CA 91330-8262, USA, Fax (818) 677-2912, E-mail jeff.charonnat@csun.edu
Further Information

Publication History

Publication Date:
31 December 2000 (online)

  PDF Download  Permissions and Reprints All articles of this category

Hydrolysis of the enol ethers 9a and 9b gave the aldehyde 10 which cyclized in situ to the alcohols 11a and 11b via an intramolecular Prins reaction. Further regio- and stereocontrolled elaboration of the alcohols 11a and 11b afforded the lactone diol 14.

intramolecular Prins - diastereoselective osmylation - (-)-anisatin