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Electrophilic substitution reactions in 4 H ‐benzo[ d,e,f ]carbazole
Author(s) -
Hoellinger H.,
BuuHoï N. P.,
Mabille Ph.
Publication year - 1969
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.5570060324
Subject(s) - chemistry , nitration , electrophilic substitution , electrophile , carbazole , halogenation , electrophilic aromatic substitution , derivative (finance) , substitution reaction , medicinal chemistry , nitrosation , nucleophilic substitution , friedel–crafts reaction , stereochemistry , organic chemistry , financial economics , economics , catalysis
The behavior of 4 H ‐benzo[ d,e,f ]earbazole and its N ‐aeetyl derivative in various electrophilic substitution reactions (e.g. nitration, nitrosation, bromination, Friedel‐Crafts acylations) has been investigated, and a number of new derivatives of this heterocycle (some of which are to be tested as potential carcinogens and enzyme‐inducers) have been synthesized.