Open Access(–)‐(4 R ,5 S )‐4‐Methyl‐3‐[2( S )‐phenoxypropionyl]‐5‐phenyloxazolidin‐2‐one
Author(s) -
Chavda Sameer,
Eames Jason,
Motevalli Majid,
Malatesti Nela
Publication year - 2006
Publication title -
acta crystallographica section e
Language(s) - English
Resource type - Journals
ISSN - 1600-5368
DOI - 10.1107/s1600536806031850
Subject(s) - chemistry , medicinal chemistry , chloride , stereochemistry , organic chemistry
The title compound, C 19 H 19 NO 4 , formed from enantiomerically pure (+)‐(4 R ,5S)‐4‐methyl‐5‐phenyl‐2‐oxazolidinone and racemic 2‐phenoxypropanoyl chloride, crystallises with Z ′ = 2. The two carbonyl groups in each molecule are oriented anti to each other, while the two methyl groups are oriented syn to each other.
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