Back to Search Start Over

Total synthesis of papulacandin D

Authors :
Denmark, Scott E.
Regens, Christopher S.
Kobayashi, Tetsuya
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