Synthesis of 4-amino-substituted tetrahydropyrimido[4,5-d]azocines

A method for the preparation of 4-amino-substituted tetrahydropyrimido[4,5- d]azocines containing an aromatic pyrimidine fragment has been developed. It was established that tetrahydropyrido[4,3-d]pyri-midines are cleaved by the action of activated alkynes with the formation of 6-vinylpyrimidines. © 2013 Springer Science+Business Media New York.

Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
8
Language
English
Pages
1180-1187
Status
Published
Volume
49
Year
2013
Organizations
  • 1 Peoples' Friendship University of Russia, 6 Miklukho-Maklaya St., Moscow 117198, Russian Federation
  • 2 Photochemistry Center, Russian Academy of Sciences, 7a Novatorov St., Moscow 119421, Russian Federation
Keywords
4-amoinopyrimidoazocine; Hofmann cleavage; ring cleavage; ring enlargement; tandem transformation; vinylpyrimidine
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/1969/
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