Asymmetric Synthesis of Alanine by Hydrogenolytic Asymmetric Transamination between (R)-2-Amino-2-phenylethanol and Ethyl Pyruvate
- 1 April 1979
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 52 (4) , 1227-1228
- https://doi.org/10.1246/bcsj.52.1227
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Syntheses of Optically Active α-Amino Acids from Esters of α-Keto Acids by Hydrogenolytic Asymmetric Transamination, A Solvent EffectBulletin of the Chemical Society of Japan, 1970
- Sterically controlled synthesis of optically active organic compounds. VI. Solvent effect in a sterically controlled synthesis of optically active .alpha.-amino acids from .alpha.-oxo acids by reductive aminationThe Journal of Organic Chemistry, 1968
- Sterically controlled syntheses of optically active organic compounds. IV. Syntheses of optically active .alpha.-amino acids from .alpha.-oxo acids by hydrogenolytic asymmetric transaminationThe Journal of Organic Chemistry, 1967
- Die Konfiguration stickstoffhaltiger Verbindungen IV. Die absolute Konfiguration der optisch aktiven β-Amino-β-phenylpropionsäureCollection of Czechoslovak Chemical Communications, 1958