Synlett 1997; 1997(1): 69-70
DOI: 10.1055/s-1997-708
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.

Vinylcyclopropylacyl Radicals: Intramolecular Ketene Additions leading to Concise Syntheses of Cyclohexenones

Nicola Herbert, Gerald Pattenden*
  • *Department of Chemistry, Nottingham University, Nottingham NG7 2RD, England
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
22. März 2004 (online)

Treatment of a range of vinylcyclopropyl selenyl esters with Bu3SnH-AIBN produces cyclohexenone products (50-60%) via 6-exo-dig radical cyclisations involving ketene intermediates.