| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5212719 | Tetrahedron | 2017 | 9 Pages |
Abstract
A stereoselective total synthesis of 10-epi-tirandamycin E is described, employing desymmetrization protocol, ring-closing metathesis (RCM), acid-catalyzed ketalization, substrate controlled dihydroxylation and Horner-Wadsworth-Emmons olefination as key reactions.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jhillu S. Yadav, Santu Dhara, Debendra K. Mohapatra,