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(4S,5S)-4-Methyl-5-phenyl-1,3-oxazolidin-2-one

✍ Scribed by Robinson, P. D. ;Hua, D. H. ;Good, L. A. ;Wang, H. ;Meyers, C. Y.

Book ID
114510033
Publisher
International Union of Crystallography
Year
1993
Tongue
English
Weight
312 KB
Volume
49
Category
Article
ISSN
0108-2701

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ChemInform Abstract: Self-Addition Produ
ChemInform Abstract: Self-Addition Products from the Alkylation of Amino Acid-Derived Oxazolidinones: X-Ray Molecular Structures of (2R,4S,1′S)-3-Benzoyl-4-( benzoylamino(phenyl)methyl)-4-benzyl-2-phenyl-1,3-oxazolidin-5-one (IV) , (2R,4S,1′S)- (VI), and (2R,4S,1′R)-3-Benzoyl-4-(benzoylamino(phenyl) methyl)-4-isopropyl-2-phenyl-1,3-oxazolidin-5-one (VII).
✍ A. D. ABELL; J. M. TAYLOR; M. D. OLDHAM 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB
(+)-(4R,5S)-4-Methyl-5-phenyl-3-[2(S)-ph
(+)-(4R,5S)-4-Methyl-5-phenyl-3-[2(S)-phenyl­propion­yl]oxazolidin-2-one
✍ Coumbarides, Gregory S. ;Eames, Jason ;Motevalli, Majid ;Malatesti, Nela ;Yohann 📂 Article 📅 2006 🏛 International Union of Crystallography 🌐 English ⚖ 223 KB

In the title compound, C 19 H 19 NO 3 , formed from enantiomerically pure (+)-(4R,5S)-4-methyl-5-phenyl-2-oxazolidinone and racemic 2-phenylpropanoyl chloride, the two carbonyl groups are oriented anti to each other, and the two methyl groups are oriented anti to each other.