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Pyriporphyrin – A Porphyrin Homologue Containing A Built‐in Pyridine Moiety
Author(s) -
Myśliborski Radomir,
LatosGrażyński Lechosław,
Szterenberg Ludmiła
Publication year - 2006
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.200600364
Subject(s) - chemistry , moiety , pyridine , porphyrin , pyrrole , stereochemistry , medicinal chemistry , photochemistry , organic chemistry
Pyriporphyrin 1 (6,11,16,21‐tetraaryl‐22‐aza‐ m ‐benziporphyrin), the simplest homologue of 5,10,15,20‐tetraarylporphyrin can be constructed by replacement of one of the pyrrole rings of 5,10,15,20‐tetraarylporphyrin with a pyridine moiety, linked to the macrocycle through α,α′‐carbon atoms. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)