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Issue 15, 1972
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Cyclisation of a dehydropeptide derivative: a model for cypridina luciferin biosynthesis

Abstract

The structure of Cypridina luciferin suggests a biosynthesis from three amino-acids; cyclisation of a modified tripeptide proceeds in excellent yield, providing a useful route to this interesting class of compound.

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Article type: Paper
DOI: 10.1039/C39720000894
Citation: J. Chem. Soc., Chem. Commun., 1972,0, 894-895
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    Cyclisation of a dehydropeptide derivative: a model for cypridina luciferin biosynthesis

    F. McCapra and M. Roth, J. Chem. Soc., Chem. Commun., 1972, 0, 894
    DOI: 10.1039/C39720000894

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