Nitration of benzo[g]isoquinoline and its methyl-substituted derivatives

Di- and trinitro derivatives are formed in the nitration under mild conditions (0-5 °C) of benzo[g]isoquinoline and its analogs with a methyl substituent in the pyridine and phenylene rings. The principal reaction products contain a nitro group in the meso position (attached to the C5 atom) and in the phenylene ring. The structures of the nitro derivatives obtained and the position of the nitro groups in the molecules were proved by means of the PMR, IR, and mass spectra. © 1982 Plenum Publishing Corporation.

Authors
Prostakov N.S. 1 , Datta Rai G. , Sergeeva N.D. 1 , Kuznetsov V.I. 1
Editors
-
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
12
Language
English
Pages
1217-1220
Status
Published
Department
-
Number
-
Volume
17
Year
1981
Organizations
  • 1 Patrice Lumumba 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/1483/