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Total synthesis of bleomycin A(sub 2) and related agents. 4. Synthesis of the disaccharide subunit: 2-O-(3-O-carbamoyl-alpha-D-mannopyranosyl)-L-gulopyranose and completion of the total synthesis of bleomycin A(sub 2)

Authors :
Boger, Dale L.
Honda, Takeshi
Source :
Journal of the American Chemical Society. June 29, 1994, Vol. 116 Issue 13, p5647, 10 p.
Publication Year :
1994

Abstract

The total synthesis of bleomycin A (sub 2) involves the incorporation of the disaccharide subunit 2-O-(3-O-carbamoyl-alpha-D-mannopyranosyl)- L-gulopyranose into the procedure. A diasteroselective alpha-O-glycosidation is the vital step for the synthesis of the disaccharide. Order of assemblage of subunits is critical for the total synthesis of bleomycin A(sub 2).

Details

ISSN :
00027863
Volume :
116
Issue :
13
Database :
Gale General OneFile
Journal :
Journal of the American Chemical Society
Publication Type :
Academic Journal
Accession number :
edsgcl.15626791