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Synthesis of 4 H ‐furo[3,2‐ b ]indoles. II . Bromination, acylation and nitration of 4 H ‐ and 4‐benzoylfuro[3,2‐ b ]indoles
Author(s) -
Tanaka Akira,
Yakushijin Kenichi,
Yoshina Shigetaka
Publication year - 1978
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.5570150126
Subject(s) - chemistry , nitration , halogenation , acylation , organic chemistry , medicinal chemistry , stereochemistry , catalysis
Monobromination and monoacylation at the 2‐position of 4 H ‐furo[3,2‐ b ]indole ring (III) were facilitated by the benzoyl group in the 4‐position; subsequent nitration attempts were unsuccessful.
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