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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 Full article

Journal Tetrahedron Letters
ISSN: 0040-4039 , E-ISSN: 1873-3581
Output data Year: 2005, Volume: 46, Number: 37, Pages: 6389-6393 Pages count : 5 DOI: 10.1016/j.tetlet.2005.05.101
Authors Elinson Michail N. 1 , Feducovich Sergey K. 1 , Starikova Zoya A. 2 , Vereshchagin Anatolii N. 1 , Gorbunov Sergey V. 1 , Nikishin Gennady I. 1
Affiliations
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

Abstract: 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.
Cite: 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
Identifiers:
Web of science: WOS:000231406400048
Scopus: 2-s2.0-23744467970
OpenAlex: W2952229275
Citing:
DB Citing
OpenAlex 41
Scopus 41
Web of science 40
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