| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5276620 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
A convergent stereoselective total synthesis of (+)-anamarine via cross-metathesis (CM) protocol starting from 2-butyn-1,4-diol and vinyl lactone is reported. Other key features of the strategy include the use of Sharpless asymmetric epoxidation, Sharpless dihydroxylation, and Red-Al reduction.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Gowravaram Sabitha, C. Nagendra Reddy, Peddabuddi Gopal, J.S. Yadav,