Yadav, J. S. ; Subba Reddy, U. V. ; Anusha, B. ; Subba Reddy, B. V. (2010) The stereoselective total synthesis of (+)-garvensintriol Tetrahedron Letters, 51 (42). pp. 5529-5531. 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.2010.07.158
Abstract
A simple and highly efficient stereoselective total synthesis of (+)-garvensintriol, isolated from the stem bark of Goniothalamus arvensis, is described using Sharpless kinetic resolution, MacMillan α-hydroxylation, and Horner-Wadsworth-Emmons olefination as the key steps.
Item Type: | Article |
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Source: | Copyright of this article belongs to Elsevier Science. |
Keywords: | Sharpless Kinetic Resolution; Stereoselective Epoxide Opening; Macmillan α-hydroxylation; Horner-Wadsworth-Emmons Reaction; Styryl Lactones |
ID Code: | 58815 |
Deposited On: | 02 Sep 2011 03:41 |
Last Modified: | 02 Sep 2011 03:41 |
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