Stereoselective electrocatalytic transformation of arylidenemalononitriles and malononitrile into (1R,5S,6R)*-6-aryl-2-amino-4,4-dialkoxy-1,5-dicyano-3-azabicyclo[3.1.0]hex-2-enes

Stereoselective electrocatalytic transformation of arylidenemalononitriles and malononitrile into (1R,5S,6R)*-6-aryl-2-amino-4,4-dialkoxy-1,5-dicyano-3-azabicyclo[3.1.0]hex-2-enes Научная публикация

Журнал

Tetrahedron
ISSN: 0040-4020 , E-ISSN: 1464-5416

Вых. Данные

Год: 2004, Том: 60, Номер: 51, Страницы: 11743-11749 Страниц : 7 DOI: 10.1016/j.tet.2004.10.003

Авторы

Elinson Michail N. ¹ , Feducovich Sergey K. ¹ , Starikova Zoya A. ² , Vereshchagin Anatolii N. ¹ , Nikishin Gennady I. ¹

Организации

1	N. D. Zelinsky Institute of Organic Chemistry, Leninsky Prospect 47, 119991 Moscow, Russian Federation
2	A. N. Nesmeyanov Institute of Organoelement Compounds, ul. Vavilova 28, 119991 Moscow, Russian Federation

Electrolysis of arylidenemalononitriles and malononitrile in alcohols in an undivided cell in the presence of sodium bromide as mediator results in the stereoselective formation of (1R,2S,6R)*-6-aryl-2-amino-4,4-dialkoxy-1,5-dicyano-3-azabicyclo[3.1.0]hex-2-enes in 60–80% yields.

Elinson M.N. , Feducovich S.K. , Starikova Z.A. , Vereshchagin A.N. , Nikishin G.I.
Stereoselective electrocatalytic transformation of arylidenemalononitriles and malononitrile into (1R,5S,6R)*-6-aryl-2-amino-4,4-dialkoxy-1,5-dicyano-3-azabicyclo[3.1.0]hex-2-enes
Tetrahedron. 2004. V.60. N51. P.11743-11749. DOI: 10.1016/j.tet.2004.10.003 WOS Scopus OpenAlex

Web of science:	WOS:000225311400008
Scopus:	2-s2.0-8444233543
OpenAlex:	W2949834021

БД	Цитирований
OpenAlex	29
Scopus	34
Web of science	33