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