Subba Reddy, B. V. ; Phaneendra Reddy, B. ; Pandurangam, T. ; Yadav, J. S. (2011) The stereoselective total synthesis of (−)-cleistenolide Tetrahedron Letters, 52 (18). pp. 2306-2308. 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.2011.02.025
Abstract
The stereoselective total synthesis of (−)-cleistenolide is described employing the Barbier allylation, MacMillan α-hydroxylation, Stille-Gennari olefination, and CeCl3·7H2O mediated lactonization as key steps.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Cleistenolide; α,β-unsaturated-δ-lactones; Macmillan α-hydroxylation; Stille-Gennari Reaction |
| ID Code: | 58769 |
| Deposited On: | 02 Sep 2011 03:42 |
| Last Modified: | 02 Sep 2011 03:42 |
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