| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5230233 | Tetrahedron | 2007 | 12 Pages |
Abstract
An efficient and versatile method for the asymmetric reduction of α- and β-ketophosphonates using chiral reactant 7 derived from sodium borohydride and d-(â)- or l-(+)-tartaric acid is developed. The methodology was applied for the preparation of bioactive products: 2,3-epoxyphosphonates, 2,3-aziridinophosphonates, phospho-GABOB, phospho-carnitine, etc.
Related Topics
Physical Sciences and Engineering
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Authors
V.V. Nesterov, O.I. Kolodiazhnyi,