The Synthesis of Optically-active Valine by the Stereoselective Decarboxylation of α-(α-Methylbenzylamino)-α-isopropylmalonic Acid
- 1 June 1973
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 46 (6) , 1886-1887
- https://doi.org/10.1246/bcsj.46.1886
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Asymmetric synthesis of .alpha.-amino acids. I. A new approachJournal of the American Chemical Society, 1970
- Asymmetric synthesis of .alpha.-amino acids. II. New systems for highly specific asymmetric synthesis with conservation of the chiral reagentJournal of the American Chemical Society, 1970
- 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
- Stereospecific hydrogenations III: Palladium-on-poly-γ-benzyl-S-glutamate and Palladium-on-Poly-β-benzyl-S-aspartateJournal of Pharmaceutical Sciences, 1969
- Syntheses of Optically Active α-Amino-acids from α-Keto-acids by Hydrogenolytic Asymmetric TransaminationNature, 1966
- Azomethine Chemistry. I. Formation of Optically Active α-Amino Acids by Asymmetric Induction1Journal of the American Chemical Society, 1961
- A Sterically Controlled Synthesis of Amino AcidsJournal of the American Chemical Society, 1961
- Asymmetric Synthesis of Threonine by Optically Active Complex Ions of CobaltBulletin of the Chemical Society of Japan, 1959
- Preparation and Properties of 2,4-Dinitrophenyl-L-amino AcidsJournal of the American Chemical Society, 1954
- Über einige Amide von AminosäurenEuropean Journal of Inorganic Chemistry, 1908