Issue 11, 1971

Electrolytic oxidation of armepavine and its derivatives

Abstract

Electrolytic oxidation of armepavine and N-norarmepavine leads to fragmentation, but the oxidation of N-carbethoxy-N-norarmepavine yields carbon–carbon dimers and, for the first time, the carbon–oxygen dimer akeleton of the alkaloid, dauricine.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 543-544

Electrolytic oxidation of armepavine and its derivatives

J. M. Bobbitt and R. C. Hallcher, J. Chem. Soc. D, 1971, 543 DOI: 10.1039/C29710000543

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