Title of article
Synthesis of (−)-(4R,5R)-muricatacin using a regio- and stereospecific ring-opening of a vinyl epoxide
Author/Authors
Baylon، نويسنده , , Christophe and Prestat، نويسنده , , Guillaume and Heck، نويسنده , , Marie-Pierre and Mioskowski *، نويسنده , , Charles، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2000
Pages
3
From page
3833
To page
3835
Abstract
Total synthesis of (−)-muricatacin, a natural acetogenin, has been achieved using as a key step a regio- and stereospecific ring-opening of a substituted vinyl epoxide under Lewis acid catalysis.
Keywords
Acetogenin , muricatacin , epoxide , ring-opening
Journal title
Tetrahedron Letters
Serial Year
2000
Journal title
Tetrahedron Letters
Record number
1637630
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