A stereoselective synthesis of the C-10 to C-18 (right half) fragment of mycalamides employing Lewis acid promoted intermolecular aldol reaction

Authors
Toyota, M Hirota, M Hirano, H Ihara, M
Citation
M. Toyota et al., A stereoselective synthesis of the C-10 to C-18 (right half) fragment of mycalamides employing Lewis acid promoted intermolecular aldol reaction, ORG LETT, 2(14), 2000, pp. 2031-2034
Citations number
22
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANIC LETTERS
ISSN journal
15237060 → ACNP
Volume
2
Issue
14
Year of publication
2000
Pages
2031 - 2034
Database
ISI
SICI code
1523-7060(20000713)2:14<2031:ASSOTC>2.0.ZU;2-M
Abstract
GRAPHICS Beginning with D-mannitol, a stereoselective synthesis of the right half se gment of the mycalamides has been accomplished by employing Lewis acid cata lyzed intermolecular aldol reaction and oxypalladation as the key steps.