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
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
Journal title :
Tetrahedron Letters
