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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Doi:10.1039/c39870000877
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(2020)Doi:10.1039/b810414j
(2009)Doi:10.1002/ejic.200701098
(2008)Doi:10.1016/j.jorganchem.2007.01.002
(2007)Doi:10.1080/00222890109601919
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