Title of article
The stereoselective total synthesis of (+)-garvensintriol
Author/Authors
Yadav، نويسنده , , J.S and Subba Reddy، نويسنده , , U.V. and Anusha، نويسنده , , B. and Subba Reddy، نويسنده , , B.V.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2010
Pages
3
From page
5529
To page
5531
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.
Keywords
MacMillan ?-hydroxylation , Horner–Wadsworth–Emmons reaction , styryl lactones , Stereoselective epoxide opening , Sharpless kinetic resolution
Journal title
Tetrahedron Letters
Serial Year
2010
Journal title
Tetrahedron Letters
Record number
1875065
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