| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1345860 | Tetrahedron: Asymmetry | 2012 | 4 Pages |
Abstract
The stereoselective total synthesis of (â)-varitriol has been achieved starting from commercially available d-(â)-ribose and o-anisic acid. A Mitsunobu reaction, Julia-Kocienski olefination, and one pot reduction of both ester and iodo functionalities with superhydride are the key reactions involved in this synthesis.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
K. Vamshikrishna, P. Srihari,