Indolopyridines with a hetero atom at a position of fusion. 7. Electrophilic substitution in 5,6-dihydroindolo-[2,1-a]isoquinoline

Halogenation, acylation, azo coupling, and alkylaminomethylation of 5,6-dihydroindoto[2,I-alisoguinoline were carried out at the C(11) position (pyrrole fragment). In dibromination, the second bromine atom was introduced into the C(9) position (indole part of the molecule). © 1994 Plenum Publishing Corporation.

Editors
-
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
2
Language
English
Pages
196-199
Status
Published
Department
-
Number
-
Volume
30
Year
1994
Organizations
  • 1 Russian Peoples' Friendship 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/955/