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.

Авторы
Prostakov N.S. 1 , Kuznetov V.I.1 , Ryashentseva M.A. 1 , Kirillova L.M. 1
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
4
Язык
Английский
Страницы
421-423
Статус
Опубликовано
Том
15
Год
1979
Организации
  • 1 Patrice Lumumba International Friendship University, Moscow, 117302, Russian Federation
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