Srikrishna, A. ; Srinivasa Rao, M. (2004) The first total synthesis of the antimicrobial sesquiterpenes (±)-enokipodins A and B Synlett (2). 0374-0376. ISSN 0936-5214
Full text not available from this repository.
Official URL: https://www.thieme-connect.com/ejournals/abstract/...
Related URL: http://dx.doi.org/10.1055/s-2003-45003
Abstract
Efficient first total synthesis of antimicrobial sesquiterpenes enokipodins A and B (1 and 2, respectively) and formal total synthesis of cuparene-1,4-diol (5) and cuparene-1,4-quinone (7) have been accomplished starting from 2,5-dimethoxy-4-methyl-acetophenone employing Claisen rearrangement and ring-closing metathesis reaction as key steps.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Thieme Medical Publishers. |
| Keywords: | Sesquiterpenes; Enokipodins A and B; Ring-closing Metathesis; Claisen Rearrangement |
| ID Code: | 48809 |
| Deposited On: | 15 Jul 2011 12:30 |
| Last Modified: | 15 Jul 2011 12:30 |
Repository Staff Only: item control page
