TOTAL SYNTHESIS OF (+ -)-METHYLENOLACTOCIN BY RADICAL CYCLIZATION OF AN EPOXIDE USING A TRANSITION-METAL RADICAL/

Authors
MAITI G ROY SC
Citation
G. Maiti et Sc. Roy, TOTAL SYNTHESIS OF (+ -)-METHYLENOLACTOCIN BY RADICAL CYCLIZATION OF AN EPOXIDE USING A TRANSITION-METAL RADICAL/, Journal of the Chemical Society. Perkin transactions. I, (5), 1996, pp. 403-404
Citations number
25
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of the Chemical Society. Perkin transactions. I → ACNP
ISSN journal
0300922X
Issue
5
Year of publication
1996
Pages
403 - 404
Database
ISI
SICI code
0300-922X(1996):5<403:TSO(-B>2.0.ZU;2-E
Abstract
A stereoselective total synthesis of (+/-)-methylenotocin 1 is achieve d via the radical cyclisation of an epoxide as a key step, using a tit anium radical source.