Issue 22, 1979

Electrophilic deuteriation of natural porphyrin derivatives

Abstract

The proportion of electrophilic deuteriation at individual meso positions in unsymmetrically substituted porphyrins depends upon the nature of the substituents on the adjacent pyrrolic subunits; in the case of protoporphyrin-IX, these observations allow the first unequivocal assignment of all four meso protons in the n.m.r. spectrum of dicyanoferriprotoheme.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1979, 1001-1003

Electrophilic deuteriation of natural porphyrin derivatives

K. M. Smith, K. C. Langry and J. S. de Ropp, J. Chem. Soc., Chem. Commun., 1979, 1001 DOI: 10.1039/C39790001001

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