Yadav, J. S. ; Sridhar Reddy, M. ; Prasad, A. R. (2006) Stereoselective syntheses of (−)-tetrahydrolipstatin via Prins cyclisations Tetrahedron Letters, 47 (29). pp. 4995-4998. ISSN 0040-4039
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tetlet.2006.05.116
Abstract
Stereoselective syntheses of (−)-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.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Anti-obesity; Homoallylic Alcohol; Prins Cyclisation and Allylic Cleavage |
| ID Code: | 58886 |
| Deposited On: | 02 Sep 2011 03:22 |
| Last Modified: | 02 Sep 2011 03:22 |
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