Yadav, J. S. ; Mandal, S. S. ; Reddy, J. S. S. ; Srihari, P. (2011) Stereoselective total synthesis of (+)-sapinofuranone B Tetrahedron, 67 (25). pp. 4620-4627. ISSN 0040-4020
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tet.2011.04.072
Abstract
Two approaches for the total synthesis of (+)-sapinofuranone B have been described. The first strategy utilizes the methodology developed earlier in our group to get the chiral propargyl alcohol and the second strategy involves generation of threo-1,2-diol derivative by diastereoselective and enantioselective addition of [(Z)-γ-methoxymethoxyallyl]diisopinocampheylborane onto aldehyde and cross metathesis as the key steps.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| ID Code: | 58816 |
| Deposited On: | 02 Sep 2011 03:42 |
| Last Modified: | 02 Sep 2011 03:42 |
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