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
Lapidus A.L. 1, 2 , Soldatenkov A.T. 1, 2 , Pirozhkov S.D. 1, 2 , Salekhuddin M. 1, 2 , Bagdadi M.V. 1, 2 , Prostakov N.S. 1, 2
Journal
Chemistry of Heterocyclic Compounds
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
1
Language
English
Pages
71-73
Status
Published
Link
External link
DOI
10.1007/BF00512819
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
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/1435/
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