Electrophilic substitution reactions in 4 H ‐benzo[ d,e,f ]carbazole | Zendy

Hoellinger H. | Zendy; BuuHoï N. P. | Zendy; Mabille Ph. | Zendy

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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.

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