Prasad, Kavirayani R. ; Mothish Kumar, S. (2013) An expeditious enantiospecific total synthesis of (–)-crassalactone C Synthesis, 45 (06). pp. 785-790. ISSN 0039-7881
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Official URL: https://www.thieme-connect.com/products/ejournals/...
Related URL: http://dx.doi.org/10.1055/s-0032-1318303
Abstract
A concise and expeditious approach for the total synthesis of bioactive styryllactone (–)-crassalactone C is presented from tartaric acid. The main features of the synthesis include the desymmetrization of dimethylamide of tartaric acid and the effective use of cinnamoyl ester as a protecting group as well as a reactant in the ring-closing metathesis reaction.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Thieme Medical Publishers Inc. |
| Keywords: | Crassalactone C; Natural Products; Stereoselective Synthesis; Styryllactone |
| ID Code: | 105648 |
| Deposited On: | 21 Dec 2017 12:05 |
| Last Modified: | 21 Dec 2017 12:05 |
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