Sabitha, Gowravaram ; Reddy, Nandyala M. ; Prasad, Muddala N. ; Yadav, Jhillu S. (2009) Stereoselective routes for the total synthesis of (+)-cryptocarya diacetate Helvetica Chimica Acta, 92 (5). pp. 967-976. ISSN 0018-019X
Full text not available from this repository.
Official URL: http://onlinelibrary.wiley.com/doi/10.1002/hlca.20...
Related URL: http://dx.doi.org/10.1002/hlca.200800355
Abstract
A stereoselective total synthesis of (+)-cryptocarya diacetate (1) was achieved by two different routes (Schemes 2 and 3). The sequences involve LiAlH4/LiI reduction, ring-closing metathesis, Prins cyclization, Wacker oxidation, and Wittig olefination reactions as key steps.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to John Wiley and Sons. |
| Keywords: | Stereoselective Synthesis; Cryptocarya Diacetate; Prins Cyclization; Wacker Oxidation; Wittig Olefination |
| ID Code: | 62955 |
| Deposited On: | 24 Sep 2011 05:00 |
| Last Modified: | 24 Sep 2011 05:00 |
Repository Staff Only: item control page
