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Facile aerial oxidation of a porphyrin. Part 18 . N ‐alkylation of the oxidised product derived from Meso ‐tetrakis(3,5‐di‐ t ‐butyl‐4‐hydroxyphenyl)porphyrin
Author(s) -
Milgrom Lionel R.,
Hill Jonathan P.,
Yahioglu Gokhan
Publication year - 1995
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570320117
Subject(s) - chemistry , alkylation , porphyrin , product (mathematics) , medicinal chemistry , polymer chemistry , organic chemistry , catalysis , geometry , mathematics
In basic solutions, the oxidised porphyrin 2 readily undergoes macrocyclic N ‐alkylation, with up to four bulky alkyl groups, including decyl and substituted benzyl moieties, being accomodated: an argument is presented to show that N ‐di‐alkylation occurs on opposite nitrogen atoms, on the same side of the macrocycle.

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