| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1350730 | Tetrahedron: Asymmetry | 2006 | 8 Pages |
Abstract
A stereoselective total synthesis of microcarpalide using ring-closing metathesis (RCM) as a key step is reported. l-Ascorbic acid was used as a chiral pool material for the construction of the olefinic alcohol and an asymmetric aldol reaction provided the chiral precursor for the synthesis of olefinic acid.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
G.V.M. Sharma, Govardhan R. Cherukupalli,