Peculiarities of the cascade cleavage of the polarized C C-fragment in alpha-ketoacetylenes on reaction with ethylene diamine Научная публикация
Журнал |
ARKIVOC
ISSN: 1551-7004 , E-ISSN: 1551-7012 |
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Вых. Данные | Год: 2014, Страницы: 132-144 Страниц : DOI: 10.3998/ark.5550190.p008.663 | ||||||||
Ключевые слова | alpha-Ketoacetylenes; ethylenediamine; Michael addition; triple bond cleavage; arylmethylketones; 4,5-dihydro-1H-imidazoles | ||||||||
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Реферат:
The reaction of diarylketoacetylenes with ethylenediamine (EDA) leads to arylmethylketones and 2-substituted imidazoline derivatives. This transformation involves complete cleavage of the triple bond via initial intermolecular Michael-addition with subsequent intramolecular Michael-addition. Final fragmentation can be presented as a retro-Mannich reaction, accompanied by three formal reductive stages (formation of three C-H bonds), while the other carbon undergoes a formal oxidation, in which three C-N bonds (C-N and C=N) are formed.
Библиографическая ссылка:
Vasilevsky S.F.
, Davydova M.P.
, Tomilin D.N.
, Sobenina L.N.
, Mamatuyk V.I.
, Pleshkova N.V.
Peculiarities of the cascade cleavage of the polarized C C-fragment in alpha-ketoacetylenes on reaction with ethylene diamine
ARKIVOC. 2014. P.132-144. DOI: 10.3998/ark.5550190.p008.663 WOS Scopus РИНЦ
Peculiarities of the cascade cleavage of the polarized C C-fragment in alpha-ketoacetylenes on reaction with ethylene diamine
ARKIVOC. 2014. P.132-144. DOI: 10.3998/ark.5550190.p008.663 WOS Scopus РИНЦ
Файлы:
Полный текст от издателя
Даты:
Опубликована online: | 19 июл. 2014 г. |
Идентификаторы:
Web of science | WOS:000345779400008 |
Scopus | 2-s2.0-84905497668 |
РИНЦ | 23978104 |
OpenAlex | W1998755221 |