| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5223034 | Tetrahedron | 2011 | 6 Pages |
Abstract
Diastereoselective Michael additions of 2-hydrogeno-2-oxo-1,4,2-oxazaphosphinanes to olefins were described. Phosphinopeptide compounds were obtained in very good yield (up to 90%) and diasteromeric excesses ranging from 26 to 78%.
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Chemistry
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