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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

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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.

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What this paper is about

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

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Available abstract

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

Key concepts: Transamination, Chemistry, Amino acid, Imine, Optically active, Organic chemistry, Stereochemistry, Catalysis

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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 — Research Paper | ScholarLens