Yadav, J. S. ; Ather, Hissana ; Uma Gayathri, K. ; Venkateswar Rao, N. ; Prasad, A. R. (2008) Stereoselective formal synthesis of Herbarumin III via Prins Cyclization Synthesis, 24 . pp. 3945-3950. ISSN 0039-7881
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-0028-1083249
Abstract
The total synthesis of herbarumin III is described, proving the versatility of the Prins cyclization in the synthesis of natural products. The approach is convergent and highly stereoselective. Ring-closing metathesis and alkene-rearrangement reactions are utilized as key steps in the synthesis of the macrolactone.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Thieme Medical Publishers. |
| Keywords: | Herbarumins; Prins Cyclization; Alkene Rearrangement; Ring-closing Metathesis |
| ID Code: | 63188 |
| Deposited On: | 28 Sep 2011 03:35 |
| Last Modified: | 28 Sep 2011 03:35 |
Repository Staff Only: item control page
