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HERO ID
6904802
Reference Type
Journal Article
Title
REGIOSELECTIVE SYNTHESES OF 1-, 2-, 3- AND 4-AMINOINDOLO[2,3-b]QUINOXALINES
Author(s)
Jaouen, A; Helissey, P; Desbene-Finck, S; Giorgi-Renault, S; ,
Year
2008
Is Peer Reviewed?
Yes
Journal
Heterocycles
ISSN:
0385-5414
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Location
OXFORD
Volume
75
Issue
11
Page Numbers
2745-+
Language
English
DOI
10.3987/COM-08-11444
Web of Science Id
WOS:000261352200010
URL
https://www.scopus.com/inward/record.uri?eid=2-s2.0-79751505460&doi=10.3987%2fCOM-08-11444&partnerID=40&md5=81741602a5cc494f82f5b39c67fb9a0b
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Abstract
In view of the contradictory results published in the literature concerning the structure of the indoloquinoxalines obtained by condensation of isatin with an unsymmetrical benzene-1,2-diamine, regioselective syntheses of the 1-, 2-, 3-, and 4-aminoindolo[2,3-b]quinoxalines have been developed. With the four derivatives in hand, isomers obtained by direct cyclocondensations starting from amino or nitro substituted benzene-1,2-diamines could be unambiguously identified. The results of these studies show, on the one hand, that some previous findings need revision and, on the other hand, that the I-amino isomer could be prepared in one step and in 58% yield.
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