Title of article
Total synthesis of microcarpalide
Author/Authors
Gurjar، نويسنده , , Mukund K. and Nagaprasad، نويسنده , , Ravi and Ramana، نويسنده , , C.V.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2003
Pages
3
From page
2873
To page
2875
Abstract
A total synthesis of the natural product microcarpalide is described. Ring-closing metathesis of a dienic ester was used as the key step. Mannose was used as the chiral pool material for the construction of the olefinic-acid and a Sharpless asymmetric dihydroxylation reaction provided the chiral precursor for the synthesis of the olefinic-alcohol.
Journal title
Tetrahedron Letters
Serial Year
2003
Journal title
Tetrahedron Letters
Record number
1661522
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