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A synthesis of new pyrrolo[3,2‐ c ]quinolines
Author(s) -
Dudouit Fabienne,
Houssin Raymond,
Hénichart JeanPierre
Publication year - 2001
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.5570380335
Subject(s) - chemistry , moiety , stereochemistry , group (periodic table) , position (finance) , combinatorial chemistry , organic chemistry , finance , economics
A synthesis of pyrrolo[3,2‐ c ]quinolines substituted in the 7‐ and 8‐ positions by methoxy groups and in the 3‐ position by an amido group is described. The structures were designed to have a crescent shape, a planar fused cyclic moiety with two ortho methoxy groups and ionisable amino or amidinic group at pH 7.
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