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Stereoselective electrochemical transformation of alkylidenecyanoacetates and malonate into (E)-3-substituted-2-cyanocyclopropane-1,1,2-tricarboxylates Full article

Journal Tetrahedron Letters
ISSN: 0040-4039 , E-ISSN: 1873-3581
Output data Year: 2000, Volume: 41, Number: 25, Pages: 4937-4941 Pages count : 5 DOI: 10.1016/s0040-4039(00)00733-4
Authors Elinson Michail N 1 , Feducovich Sergey K 1 , Starikova Zoya A 2 , Olessova Olga S 1 , Vereshchagin Anatolii N 1 , Nikishin Gennady I 1
Affiliations
1 N.D. Zelinsky Institute of Organic Chemistry, Leninsky prospect 47, 117913 Moscow B-334, Russia
2 A.N. Nesmeyanov Institute of Organoelement Compounds, ul. Vavilova 28, 117813 Moscow B-334, Russia

Abstract: Electrolysis of malonate and alkylidenecyanoacetates in alcohols in the presence of sodium bromide in an undivided cell results in the stereoselective formation of (E)-3-substituted 2-cyanocyclopropane-1,1,2-tricarboxylates in 75–85% yields.
Cite: Elinson M.N. , Feducovich S.K. , Starikova Z.A. , Olessova O.S. , Vereshchagin A.N. , Nikishin G.I.
Stereoselective electrochemical transformation of alkylidenecyanoacetates and malonate into (E)-3-substituted-2-cyanocyclopropane-1,1,2-tricarboxylates
Tetrahedron Letters. 2000. V.41. N25. P.4937-4941. DOI: 10.1016/s0040-4039(00)00733-4 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000087794300024
Scopus: 2-s2.0-0034686211
OpenAlex: W2952535205
Citing:
DB Citing
OpenAlex 40
Scopus 39
Web of science 39
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