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Total synthesis of papulacandin D
- Source :
- Journal of the American Chemical Society. March 14, 2007, Vol. 129 Issue 10, p2774, 3 p.
- Publication Year :
- 2007
-
Abstract
- An efficient enantioselective total synthesis of papulacandin D by a convergent synthetic strategy is described. The reaction involves a silicon-based cross-coupling reaction to construct the key spirocyclic C-aryl glycopyranoside and an enatioselective allylation reaction using a chiral bisphosphoramide for the construction of the C7 stereocenter.
Details
- Language :
- English
- ISSN :
- 00027863
- Volume :
- 129
- Issue :
- 10
- Database :
- Gale General OneFile
- Journal :
- Journal of the American Chemical Society
- Publication Type :
- Academic Journal
- Accession number :
- edsgcl.163173276