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A de novo enantioselective total synthesis of (-)-laulimalide

Authors :
Nelson, Scott G.
Cheung, Wing S.
Kassick, Andrew J.
Hilfiker, Mark A.
Seagle, Paul H.
Source :
Journal of the American Chemical Society. Nov 20, 2002, Vol. 124 Issue 46, p13654, 2 p.
Publication Year :
2002

Abstract

Laulimalide is a naturally occurring microtubule-stabilizing agent first isolated from the marine sponges Hyattella sp. and Spongia mycofijiensis. A de novo enantioselective total synthesis of (-)-laulimalide is achieved. The synthesis is characterized by extensive use of new reaction methodology derived from asymmetric aldehyde cyclocondensation (AAC) reactions and ensuing transformations of the derived enantioenriched beta-lactones.

Details

Language :
English
ISSN :
00027863
Volume :
124
Issue :
46
Database :
Gale General OneFile
Journal :
Journal of the American Chemical Society
Publication Type :
Academic Journal
Accession number :
edsgcl.123529981