ChemInform Abstract: Highly Stereoselective Conjugate Addition of (R)- or (S)-4-Phenyl-2- oxazolidinone to Nitroalkenes.
β Scribed by D. LUCET; L. TOUPET; T. LE GALL; C. MIOSKOWSKI
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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π SIMILAR VOLUMES
The addition of the potassium salt of (R)-or (S)-4-phenyl-products were converted into Ξ±-amino acids and monosubstituted 1,2-diamines of high enantiomeric purity. 2-oxazolidinone to monosubstituted nitroalkenes proceeded with very good diastereoselectivity. Several of the addition derivatives are in
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