Radical Rearrangements of Vinylcyclopropanes as a Route to Bicyclic Lactones, Lactams and Ketones

M. P. Bertrand; R. Nouguier; A. Archavlis; A. Carrière

doi:10.1055/s-1994-22991

Subscribe to RSS

Please copy the URL and add it into your RSS Feed Reader.

https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000083.xml

Share / Bookmark

Facebook Linkedin Weibo

Download PDF

Synlett 1994; 1994(9): 736-738
DOI: 10.1055/s-1994-22991

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.

Radical Rearrangements of Vinylcyclopropanes as a Route to Bicyclic Lactones, Lactams and Ketones

M. P. Bertrand^* , R. Nouguier, A. Archavlis, A. Carrière

^*Laboratoire de Chimie Moléculaire Organique - URA 1412 - B 562 -Faculté des Sciences St Jérôme

Further Information

Publication History

Publication Date:
18 September 2002 (online)

PDF Download Permissions and Reprints All articles of this category

The free-radical mediated vinylcyclopropanes annulation offers an efficient route to fused or bridged bicyclic compounds via sequential radical addition, ring opening, tandem ring closures and fragmentation.