| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5261353 | Tetrahedron Letters | 2014 | 5 Pages |
Abstract
A stereoselective total synthesis of L-783,290 has been achieved involving Alder-Rickert reaction, ring closing metathesis, and chemoselective oxidation as key steps. This approach has successfully demonstrated a linear sequence of reactions, which are highly stereoselective for the construction of the resorcylic acid unit.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
A. Srinivas Reddy, Ch. Kishore, B.V. Subba Reddy,