| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5279198 | Tetrahedron Letters | 2007 | 5 Pages |
Abstract
A simple carbohydrate based convergent approach towards the total synthesis of (â)-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.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
P. Srihari, B. Prem Kumar, K. Subbarayudu, J.S. Yadav,