Title of article
Total synthesis of (−)-microcarpalide from d-mannitol
Author/Authors
Ghosh، نويسنده , , Subhash and Rao، نويسنده , , R. Vengal and Shashidhar، نويسنده , , J.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2005
Pages
3
From page
5479
To page
5481
Abstract
The total synthesis of the actin-targeting metabolite (−)-microcarpalide is described. Ring-closing metathesis of a dienic ester was used as the key step. d-Mannitol was used as the chiral pool material for the construction of the olefinic acid moiety as well as the olefinic alcohol moiety of the molecule.
Keywords
ring-closing metathesis , d-Mannitol , Microcarpalide , allylation
Journal title
Tetrahedron Letters
Serial Year
2005
Journal title
Tetrahedron Letters
Record number
1846381
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