N-Chloroacyl Derivatives of Valine Esters
β Scribed by V. A. Knizhnikov; V. I. Potkin; K. A. Zhavnerko; L. S. Yakubovich; S. K. Petkevich; S. P. Kacherskaya
- Book ID
- 110395246
- Publisher
- SP MAIK Nauka/Interperiodica
- Year
- 2002
- Tongue
- English
- Weight
- 25 KB
- Volume
- 38
- Category
- Article
- ISSN
- 1070-4280
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π SIMILAR VOLUMES
The crystal structure of the title compound, C 15 H 19 NO 3 , shows that the overall molecular conformation, which is approximately planar, is stabilized by intermolecular N-HΓ Γ ΓO hydrogen-bonding interactions.
There are extensive reports on the deamlnatlone of a-amino aclde and their esters, and the deaminatione of a-amino acids are generally recognized to occur with retention of configuration due to the participation of the neighboring carboxylate group, while the deaminatlons of a-amino acid eetere proc