The stereoselective total synthesis of (+)-garvensintriol

Yadav, J. S. ; Subba Reddy, U. V. ; Anusha, B. ; Subba Reddy, B. V. (2010) The stereoselective total synthesis of (+)-garvensintriol Tetrahedron Letters, 51 (42). pp. 5529-5531. 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.2010.07.158

Abstract

A simple and highly efficient stereoselective total synthesis of (+)-garvensintriol, isolated from the stem bark of Goniothalamus arvensis, is described using Sharpless kinetic resolution, MacMillan α-hydroxylation, and Horner-Wadsworth-Emmons olefination as the key steps.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Sharpless Kinetic Resolution; Stereoselective Epoxide Opening; Macmillan α-hydroxylation; Horner-Wadsworth-Emmons Reaction; Styryl Lactones
ID Code:58815
Deposited On:02 Sep 2011 03:41
Last Modified:02 Sep 2011 03:41

Repository Staff Only: item control page