ChemInform Abstract: ASYMMETRIC TRANSAMINATION FROM AMINO ACIDS. I. ASYMMETRIC SYNTHESIS OF AMINO ACID BY CHEMICAL TRANSAMINATION FROM OPTICALLY ACTIVE AMINO ACIDS TO α‐KETO ACID

Susumu Yamada; Shunichi Hashimoto

doi:10.1002/chin.197625193

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ChemInform Abstract: ASYMMETRIC TRANSAMINATION FROM AMINO ACIDS. I. ASYMMETRIC SYNTHESIS OF AMINO ACID BY CHEMICAL TRANSAMINATION FROM OPTICALLY ACTIVE AMINO ACIDS TO α‐KETO ACID

Susumu Yamada Shunichi Hashimoto

Year: 1976 Journal: Chemischer Informationsdienst Vol: 7 (25) Publisher: Wiley

DOI: 10.1002/chin.197625193

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Abstract

Abstract Aus Brenztraubensäuremethylester (I) und den L‐Aminosäureestern (II) entstehen Imine (III), die nach katalytischer Hydrierung ein Diastereomerengemisch (IV) geben.

Keywords:

Transamination Chemistry Amino acid Imine Optically active Organic chemistry Stereochemistry Catalysis Biochemistry

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Chemical Synthesis and Analysis

Life Sciences → Biochemistry, Genetics and Molecular Biology → Molecular Biology

Asymmetric Hydrogenation and Catalysis

Physical Sciences → Chemistry → Inorganic Chemistry

Synthesis and Catalytic Reactions

Physical Sciences → Chemistry → Organic Chemistry

ChemInform Abstract: ASYMMETRIC TRANSAMINATION FROM AMINO ACIDS. I. ASYMMETRIC SYNTHESIS OF AMINO ACID BY CHEMICAL TRANSAMINATION FROM OPTICALLY ACTIVE AMINO ACIDS TO α‐KETO ACID

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