Title
Electrophilic deuteriation of natural porphyrin derivatives
Document Type
Article
Publication Date
12-1-1979
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.
Publication Source (Journal or Book title)
Journal of the Chemical Society, Chemical Communications
First Page
1001
Last Page
1003
Recommended Citation
Smith, K., Langry, K., & De Ropp, J. (1979). Electrophilic deuteriation of natural porphyrin derivatives. Journal of the Chemical Society, Chemical Communications (22), 1001-1003. https://doi.org/10.1039/C39790001001
COinS