AN ENANTIOSELECTIVE APPROACH TO THE SYNTHESIS OF POLYCYCLIC ETHERS

Citation
Vs. Martin et al., AN ENANTIOSELECTIVE APPROACH TO THE SYNTHESIS OF POLYCYCLIC ETHERS, Anales de quimica, 89(1), 1993, pp. 67-72
Citations number
30
Categorie Soggetti
Chemistry
Journal title
ISSN journal
11302283
Volume
89
Issue
1
Year of publication
1993
Pages
67 - 72
Database
ISI
SICI code
1130-2283(1993)89:1<67:AEATTS>2.0.ZU;2-S
Abstract
The enantiomeric synthesis by intramolecular hetero-Michael additions of polysubstituted and polycyclic ethers present in marine toxins is d escribed. The stereoselectivity in the cyclization steps is governed b y the double bond geometry of the electrophylic double bond. A silicon assistance observed in the cyclization step led to the stereocontroll ed synthesis of oxepanes.