Title of article
A formal stereoselective synthesis of (−)-brevisamide
Author/Authors
Yadav، نويسنده , , J.S. and Raju، نويسنده , , A. and Ravindar، نويسنده , , K. and Subba Reddy، نويسنده , , B.V.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2013
Pages
3
From page
3227
To page
3229
Abstract
An efficient stereoselective formal synthesis of marine derived monocyclic ether (−)-brevisamide is reported. The key steps involved in this synthesis are syn-Aldol reaction, Sharpless asymmetric epoxidation, and stereoselective construction of tetrahydropyran ring by 6-endo-cyclization of suitably substituted hydroxy styrylepoxide.
Keywords
Brevisamide , Wittig reaction , Sharpless asymmetric epoxidation , syn-Aldol reaction , 6-endo-Cyclization
Journal title
Tetrahedron Letters
Serial Year
2013
Journal title
Tetrahedron Letters
Record number
1884709
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