Chandrasekhar, S. ; Rambabu, Ch. ; Jaya Prakash, S. (2006) Total synthesis of 6-epiprelactone-V via a syn-selective oxygen tethered intramolecular Michael reaction Tetrahedron Letters, 47 (7). pp. 1213-1215. ISSN 0040-4039
Full text not available from this repository.
Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tetlet.2005.12.012
Abstract
The intramolecular protective group (benzylidene acetal) assisted syn-1,3-diol synthesis has been efficiently utilized in a short synthesis of 6-epiprelactone-V starting from (S)-malic acid.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Keck Allylation; Intramolecular Oxy-Michael Reaction; (−)-Centrolobine; 2, 6-Disubstituted Tetrahydropyran |
| ID Code: | 62397 |
| Deposited On: | 22 Sep 2011 03:28 |
| Last Modified: | 22 Sep 2011 03:28 |
Repository Staff Only: item control page
