| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5264698 | Tetrahedron Letters | 2013 | 4 Pages |
Abstract
The first total synthesis of the pectinolide C has been accomplished using the silyl-tethered ring closing metathesis, Jacobsen resolution, and Wadsworth-Emmons olefinations as key reaction sequences.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
T. Vijaya Kumar, G. Shankaraiah, K. Suresh Babu, J. Madhusudana Rao,