2-Ammonio-3-phenylpropanoic acid–monohydrogen sulfate–2-ammonio-3-phenylpropanoate (1/1/1)
✍ Scribed by Sun, Yu-Xi ;You, Zhong-Lu
- Publisher
- International Union of Crystallography
- Year
- 2004
- Tongue
- English
- Weight
- 301 KB
- Volume
- 60
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
Single-crystal X-ray study T = 293 K Mean '(C±C) = 0.011 A Ê R factor = 0.075 wR factor = 0.163 Data-to-parameter ratio = 13.0
For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
📜 SIMILAR VOLUMES
The title compound, C 11 H 9 NO 4 , was synthesized by mixing phthalic anhydride and (S)-2-aminopropanoic acid in acetic acid. The dihedral angle between the phthalimide ring system and the O3/O4/C9/C11 plane is 86.7 (3) . The crystal structure is stabilized by weak O-HÁ Á ÁO hydrogen bonds.
In the title compound, C 28 H 27 N 3 O 3 , the pyrazolone ring and the N atom of the 2-amino-3-phenylpropanoate group are essentially coplanar. The compound is in an enamine-keto form and its structure is stabilized by one strong intramolecular N-HÁ Á ÁO hydrogen bond.
In the crystal structure of the title compound, C 15 H 16 N 2 O 3 , N-HÁ Á ÁO and O-HÁ Á ÁO hydrogen bonds link the molecules into a three-dimensional network, in which they may be effective in the stabilization of the crystal structure.
The title compound, C 25 H 29 NO 3 , was prepared from (R)-5,5dimethyl-4-phenyl-3-[(E)-3-phenylacryloyl]oxazolidin-2-one, coupled with cyclopentylmagnesium bromide via asymmetric Michael addition. The relative configuration of the chiral C atoms of the product is as expected.