Indolopyridines with a hetero atom at a position of fusion. 6. Electrophilic substitution in indolo[2,1-a]isoquinoline

Nitration, halogenation, azo coupling, aminomethylation, hydroxymethylation, and acylation reactions of indolo[2,1-a]isoquinoline in a neutral or weakly acid medium gave derivatives at the C(11) position (the pyrrole ring). Using nitrosation as an example, it was shown that electrophilic substitution at the benzene ring of the indole fragment can occur in a strongly acid medium. © 1994 Plenum Publishing Corporation.

Authors
Ntaganda G. 1 , Soldatova S.A. 1 , Rodriguez Alarcon J.A. , Anisimov B.N. 1 , Soldatenkov A.T. 1
Editors
-
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
1
Language
English
Pages
73-78
Status
Published
Department
-
Number
-
Volume
30
Year
1994
Organizations
  • 1 Russian Peoples' Freindship University, Moscow, 117923, Russian Federation
Keywords
-
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/958/