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Issue 1, 2001
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Enantioselective hydrolysis of amino acid esters by apomyoglobin: perfect kinetic resolution of a phenylalanine derivative

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Abstract

Apoprotein of horse-heart myoglobin promoted enantioselective hydrolysis of 4-nitrophenyl esters of amino acids, which allowed nearly perfect kinetic resolution of racemic N-Boc-phenylalanine ester (Boc-Phe-ONp).

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Publication details

The article was received on 18 Oct 2000, accepted on 20 Nov 2000 and first published on 18 Dec 2000


Article type: Communication
DOI: 10.1039/B008403O
Citation: Chem. Commun., 2001,0, 133-134
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    Enantioselective hydrolysis of amino acid esters by apomyoglobin: perfect kinetic resolution of a phenylalanine derivative

    K. Tomisaka, Y. Ishida, K. Konishi and T. Aida, Chem. Commun., 2001, 0, 133
    DOI: 10.1039/B008403O

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