Oxidation and hydrogenation of benzo[g]isoquinolines

The oxidation of methyl-substituted (in the pyridine and benzene rings) benzo[g]isoquinolines to substituted 2-azaanthraquinones was realized. It was established that the pyridine ring is partially reduced to give 1,2,3,4-tetrahydrobenzo[g]isoquinolines in the hydrogenation of benzo[g]isoquinolines in the presence of rhenium heptasulfide. © 1979 Plenum Publishing Corporation.

Authors
Prostakov N.S. 1 , Kuznetov V.I.1 , Ryashentseva M.A. 1 , Kirillova L.M. 1
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
4
Language
English
Pages
421-423
Status
Published
Volume
15
Year
1979
Organizations
  • 1 Patrice Lumumba International Friendship University, Moscow, 117302, Russian Federation
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/1578/
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