Conversion of 2-ethyl- 3, 3, 5, 5-tetramethyl- and 2-ethyl- 1, 3, 3, 5, 5-pentamethyl-1, 2, 4, 5-tetra- hydro-3H-benz-2-azepines by the action of ethyl propiolate

It has been shown that, on interacting 2-ethyl-3, 3, 5, 5-tetramethyl- and 2-ethyl-1, 3, 3, 5, 5-pentamethyl-1, 2, 4, 5-tetrahydro-3H-benz-2-azepines with ethyl propiolate in methanol, fission of the azepine ring occurs at the C(1)-N(2) bond involving a molecule of solvent. The indicated azepines do not react with acetylenedicarboxylic acid ester under these conditions. © 2009 Springer Science+Business Media, Inc.

Авторы
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
10
Язык
Английский
Страницы
1248-1251
Статус
Опубликовано
Том
45
Год
2009
Организации
  • 1 Peoples' Friendship University of Russia, Moscow 117198, Russian Federation
  • 2 L. M. Litvinenko Institute of Physical Organic Chemistry and Coal Chemistry, National Academy of Sciences of Ukraine, Donetsk 83114, Ukraine
Ключевые слова
Activated alkynes; Fission; Tetrahydrobenz-2-azepines
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