Download PDF
Synlett 2001; 2001(10): 1611-1613
DOI: 10.1055/s-2001-17442
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.

Intramolecular Ene Reactions for Methylenecyclohexanol Synthesis

Chi-Ming Cheung* , Donald Craig, Richard S. Todd
  • *Centre for Chemical Synthesis, Department of Chemistry, Imperial College of Science, Technology and Medicine, London SW7 2AY, UK; Fax + 44(20)75 94 58 68; E-mail: d.craig@ic.ac.uk
Further Information

Publication History

Publication Date:
27 September 2001 (online)

  PDF Download  Permissions and Reprints All articles of this category

Thermally-induced or Lewis acid-mediated intramolecular ene reactions of diastereomeric δ,ℇ-unsaturated ketones give methylenecyclohexanols in high yield and with excellent diastereoselectivity.

carbonyl ene - intramolecular - methylenecyclohexanol - stereoselectivity

      >