Issue 0, 1979

The enzymatic oxidation of phenolic tetrahydroisoquinoline-1-carboxylic acids

Abstract

Tetrahydroisoquinoline-1-carboxylic acids with a 6- or 7-hydroxy substituent undergo oxidative decarboxylation on treatment with horseradish peroxidase or fungal laccase to give high yields of the corresponding 3,4-dihydroisoquinolines. Attempts to apply this reaction to the formation of an aporphine were unsuccessful.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1979, 2744-2750

The enzymatic oxidation of phenolic tetrahydroisoquinoline-1-carboxylic acids

I. G. C. Coutts, M. R. Hamblin, E. J. Tinley and J. M. Bobbitt, J. Chem. Soc., Perkin Trans. 1, 1979, 2744 DOI: 10.1039/P19790002744

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