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Synthesis and 13 C, 15 N NMR study of a new functionalized pyrido[2,3‐ b ]indole derivative
Author(s) -
Buisson J.P.,
Bisagni E.,
Monneret C.,
Demerseman P.,
Leon C.,
Platzer N.
Publication year - 1996
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.5570330368
Subject(s) - chemistry , indole test , derivative (finance) , carbon 13 nmr , bicyclic molecule , medicinal chemistry , stereochemistry , financial economics , economics
New functionalized α‐carbolinones especially the 4‐hydroxy‐3‐nitro‐1 H ,9 H ‐pyrido[2,3‐ b ]indol‐2‐one were synthesized in a good yield, three‐step reaction. A complete 13 C, 15 N nmr study of this carbolinone and precursors is presented.
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