Premium
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)
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom