| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5227041 | Tetrahedron | 2009 | 8 Pages |
Abstract
A highly stereoselective asymmetric total synthesis of marine polypropionate (â)-baconipyrone C has been achieved. Utilization of desymmetrization technique to create five stereogenic centres, Sharpless epoxidation, Gilman's reaction and resolution of methyl group using enzyme PS-C is the highlight of the synthesis.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
J.S. Yadav, K. Sathaiah, R. Srinivas,