Versatile synthesis of L-α-amino acids stereospecifically labelled on the β-carbon atom
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
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2. Versatile synthesis of stereospecifically labelledD-amino acids via labelled aziridines—preparation of (2R,3S)-[3-2H1]- and (2R,3R)-[2,3-2H2]-serine; (2S,2′S,3S,3′S)-[3,3′-2H2]- and (2S,2′S,3R,3′R)-[2,2′,3,3′-2H4]-cystine; and (2S,3S)-[3-2H1-] and (2S,3R)-[2,3-2H2]-β-chloroalanine
3. Synthesis of stereospecifically labelled D-prop-2-ynylglycine and investigation of the action of D-amino acid oxidase
4. Stereochemistry of conversion of the suicide substrates β-chloro-D-alanine-andD- andL-serine O-sulfates into pyruvate byD-amino acid aminotransferase and byL-aspartate aminotransferase
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2. ChemInform Abstract: Versatile Synthesis of L-α-Amino Acids Stereospecifically Labeled on the β-Carbon Atom.;ChemInform;2010-08-04
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5. Stereochemistry of reactions of the inhibitor/substrates l- and d-β-chloroalanine with β-mercaptoethanol catalysed by l-aspartate aminotransferase and d-amino acid aminotransferase respectively;Organic & Biomolecular Chemistry;2005
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