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
Link To Document :
بازگشت