| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5281426 | Tetrahedron Letters | 2007 | 5 Pages |
Abstract
A chiral racemic 2-phosphono-2,3-didehydrothiolane sulfoxide was used as a Michael acceptor in the reactions with several nucleophiles, in particular thiols. In most cases the reactions were fully diastereoselective. The relative configuration of the resulting adducts was determined.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
