Srihari, P. ; Prem Kumar, B. ; Subbarayudu, K. ; Yadav, J. S. (2007) A convergent approach for the total synthesis of (−)-synrotolide diacetate Tetrahedron Letters, 48 (39). pp. 6977-6981. 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.2007.07.172
Abstract
A simple carbohydrate based convergent approach towards the total synthesis of (−)-synrotolide diacetate is described employing a Sharpless asymmetric epoxidation, a Grignard assisted lactol opening with a terminal alkyne and a Wittig reaction using the Horner-Emmons reagent as the key steps.
Item Type: | Article |
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Source: | Copyright of this article belongs to Elsevier Science. |
ID Code: | 58789 |
Deposited On: | 02 Sep 2011 03:27 |
Last Modified: | 02 Sep 2011 03:27 |
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