| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5217870 | Tetrahedron | 2013 | 5 Pages | 
Abstract
												An enantiospecific formal total synthesis of the macrolide (+)-aspicilin is accomplished from chiral pool tartaric acid. Key features of the synthesis include desymmetrization of the bis-dimethyl amide of tartaric acid and further elaboration to the title compound using olefin cross-metathesis and Yamaguchi macrolactonization as the pivotal steps.
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											Authors
												Vasudeva Rao Gandi, 
											