Chandrasekhar, S. ; Rambabu, Ch. ; Syamprasad Reddy, A. (2008) Asymmetric synthesis of (+)-passifloricin A and its 6-epimer Tetrahedron Letters, 49 (29-30). pp. 4476-4478. 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.2008.05.070
Abstract
Stereoselective total syntheses of the antiprotozoal natural product (+)-passifloricin A and its C-6 epimer have been achieved in ∼5% overall yield. The strategy is based on Jacobsen epoxidation, Grubbs' metathesis and an Evans' intramolecular oxa-Michael reaction.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Jacobsen Epoxidation; Grubbs' Metathesis; Evans' Intramolecular Oxa-Michael Reaction; Maruoka Allylation |
| ID Code: | 62355 |
| Deposited On: | 22 Sep 2011 03:34 |
| Last Modified: | 22 Sep 2011 03:34 |
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