| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5289593 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
Stereoselective syntheses of (â)-tetrahydrolipstatin have been achieved via two divergent approaches through Prins cyclisations as the key steps. PCC mediated oxidative cleavage, Frater alkylation, Keck allylation, Sharpless asymmetric epoxidation and allylic cleavage were the other key steps employed.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
J.S. Yadav, M. Sridhar Reddy, A.R. Prasad,