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Synthesis of 7 H ‐pyrido[2,3‐ c ]carbazoles from 5‐bromo‐8‐methoxyquinolines via coupling and azide cyclization reactions
Author(s) -
Trécourt Françis,
Mongin Florence,
Mallet Marc,
Quéguiner Guy
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.5570320428
Subject(s) - chemistry , azide , coupling (piping) , stereochemistry , medicinal chemistry , combinatorial chemistry , computational chemistry , organic chemistry , mechanical engineering , engineering
A new strategy for the synthesis of substituted 7 H ‐pyrido[2,3‐ c ]carbazoles has been developed from substituted 5‐bromoquinolines by using cross‐coupling reaction with (2‐aminophenyl)boric acids, followed by a regioselective azide cyclization.
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