Prasad, Kavirayani R. ; Gholap, Shivajirao L. (2005) An expeditious enantiospecific total synthesis of (+)-7-epi-goniofufurone Synlett (14). pp. 2260-2262. ISSN 0936-5214
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Official URL: https://www.thieme-connect.de/DOI/DOI?10.1055/s-20...
Related URL: http://dx.doi.org/10.1055/s-2005-871965
Abstract
Stereoselective synthesis of styryl lactone, (+)-7-epi-goniofufurone was achieved in high yield via simple transformations from tartaric acid. The key step involves the successive stereoselective reduction of ketones with borohydride and selectride.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Thieme Medical Publishers Inc. |
| Keywords: | Styryl Lactones; (+)-Goniofufurone; Stereoselective Reduction |
| ID Code: | 105967 |
| Deposited On: | 21 Dec 2017 12:06 |
| Last Modified: | 21 Dec 2017 12:06 |
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