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On the synthesis and isolation of chlorocarbazoles obtained by chlorination of N ‐substituted carbazoles
Author(s) -
Bonesi Sergio M.,
ErraBalsells Rosa
Publication year - 1997
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.5570340328
Subject(s) - chemistry , substituent , organic chemistry , medicinal chemistry
Chloro derivatives of N ‐methylcarbazole ( 1 ), N ‐phenylcarbazole ( 2 ), N ‐acetylcarbazole ( 3 ), N ‐benzoylcarbazole ( 4 ) and 2‐methoxy‐ N ‐methylcarbazole are synthesized. They are compounds 1a, 1b, 1c, 1d, 1e, 2a, 2b, 3a, 3b, 3c, 3d, 4a, 4b, 5a, 5b, 5c, 5d and 5e . Some of them are described for the first time. By using semiempirical PM3 method theoretical substituent effects on the chlorinating reaction are calculated. A chlorination mechanism of carbazoles and N ‐substituted carbazoles are compared.

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