Catalytic carbonylation of nitrobenzyl- and nitroarylpyridines

The corresponding carbamates were obtained by carbonylation in the presence of selenourea of benzyl- and aryl-substituted pyridines that contain a nitro group in the benzene ring and as a result of carbonylation of 7-nitro-1-azafluorene. The reaction is accompanied by simultaneous reduction of the nitro group to an amino group. © 1983 Plenum Publishing Corporation.

Authors
Editors
-
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
1
Language
English
Pages
71-73
Status
Published
Department
-
Number
-
Volume
19
Year
1983
Organizations
  • 1 Patrice Lumumba Peoples' Friendship University, Moscow, 117923, Russian Federation
  • 2 N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, Moscow, 117913, 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/1435/