Yadav, J. S. ; Vishweshwar Rao, K. ; Prasad, A. R. (2006) A chiron approach to (−)-tetrahydrolipstatin Synthesis, 2006 (22). pp. 3888-3894. ISSN 0039-7881
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Official URL: https://www.thieme-connect.com/ejournals/abstract/...
Related URL: http://dx.doi.org/10.1055/s-2006-950325
Abstract
An efficient chiron approach to the total synthesis of (−)-tetrahydrolipstatin is described. The main features of the synthetic strategy, which starts from tri-O-acetyl-D-glucal, are copper-mediated- C-C bond formation, Frater alkylation, and Barton-McCombie- deoxygenation.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Thieme Medical Publishers. |
| Keywords: | (−)-tetrahydrolipstatin; Anti-obesity; Tri-O-acetyl-D-glucal; Frater Alkylation |
| ID Code: | 63218 |
| Deposited On: | 28 Sep 2011 03:27 |
| Last Modified: | 28 Sep 2011 03:27 |
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