Tetrahedron Asymmetry p. 137 - 140 (1990)
Update date:2022-08-04
Topics: Yield Catalyst Enantioselective Total synthesis Stereoselective Protecting group Chiral Auxiliary Functional Group Interconversion Spectroscopic Analysis (+)-Asperlin
Ramesh
Franck
A stereochemically unambiguous synthesis of (+)-asperlin from L-rhamnose establishes the configuration of the antibiotic as 4S, 5S, 6S, 7R.
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