| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5277203 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
An enantioselective convergent approach toward the total synthesis of pinellic acid 1 from 1,9-nonanediol is described. The synthetic strategy features iterative Sharpless asymmetric dihydroxylation, Sonogashira coupling and Birch reduction.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
S. Vasudeva Naidu, Pradeep Kumar,