Issue 4, 1992

Fragmentation of laudanosine by single electron transfer reactions

Abstract

The radical cation of laudanosine, formed by a photoinduced electron transfer reaction or by oxidation with a tris(4-bromophenyl)aminium salt, undergoes cleavage of a C–C bond similar to the mass spectrometric fragmentation induced by electron ionization.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1992, 449-450

Fragmentation of laudanosine by single electron transfer reactions

S. Yamada, T. Tanaka, S. Akiyama and M. Ohashi, J. Chem. Soc., Perkin Trans. 2, 1992, 449 DOI: 10.1039/P29920000449

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