Stereoselective electrocatalytic transformation of arylidene- or alkylidenemalononitriles and malonate into alkyl (1R,5R,6R)* 6-substituted 5-cyano-4,4-dialkoxy-2-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylates

Stereoselective electrocatalytic transformation of arylidene- or alkylidenemalononitriles and malonate into alkyl (1R,5R,6R)* 6-substituted 5-cyano-4,4-dialkoxy-2-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylates Научная публикация

Журнал

Tetrahedron Letters
ISSN: 0040-4039 , E-ISSN: 1873-3581

Вых. Данные

Год: 2005, Том: 46, Номер: 37, Страницы: 6389-6393 Страниц : 5 DOI: 10.1016/j.tetlet.2005.05.101

Авторы

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

Организации

1	N. D. Zelinsky Institute of Organic Chemistry, Leninsky prospect 47, 119991 Moscow, Russia
2	A. N. Nesmeyanov Institute of Organoelement compounds, ul. Vavilova 28, 119991 Moscow, Russia

Electrolysis of arylidene- or alkylidenemalononitriles and malonate in alcohol in an undivided cell in the presence of sodium halide as mediator results in the stereoselective formation of alkyl (1R,5R,6R)* 6-substituted 5-cyano-4,4-dialkoxy-2-oxo-3-azabicyclo[3.1.0]hexan-1-carboxylates in 50–70% yields.

Elinson M.N. , Feducovich S.K. , Starikova Z.A. , Vereshchagin A.N. , Gorbunov S.V. , Nikishin G.I.
Stereoselective electrocatalytic transformation of arylidene- or alkylidenemalononitriles and malonate into alkyl (1R,5R,6R)* 6-substituted 5-cyano-4,4-dialkoxy-2-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylates
Tetrahedron Letters. 2005. V.46. N37. P.6389-6393. DOI: 10.1016/j.tetlet.2005.05.101 WOS Scopus OpenAlex

Web of science:	WOS:000231406400048
Scopus:	2-s2.0-23744467970
OpenAlex:	W2952229275

БД	Цитирований
OpenAlex	41
Scopus	41
Web of science	40