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A novel strategy of constructing the cyclohexane ring: stereoselective multicomponent cyclization of aromatic aldehydes, malononitrile, and acetone into cis-2,6-diaryl-4-dicyanomethylidenecyclohexane-1,1-dicarbonitriles Full article

Journal Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Output data Year: 2008, Volume: 57, Number: 3, Pages: 585-590 Pages count : 6 DOI: 10.1007/s11172-008-0091-y
Authors Vereshchagin A.N. 1 , Elinson M.N. 1 , Feducovich S.K. 1 , Zaimovskaya T.A. 2 , Starikova Z.A. 3 , Belyakov P.A. 1 , Nikishin G.I. 1
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation
2 A. V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, 29 Leninsky prosp., 119991, Moscow, Russian Federation
3 A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 119991, Moscow, Russian Federation

Abstract: A novel multicomponent reaction involved five organic molecules to form the cyclohexane ring. Aromatic aldehydes, malononitrile, and acetone in the presence of a catalytic amount of sodium acetate underwent stereoselective cyclization into cis-2,6-diaryl-4-dicyanomethylidenecyclohexane-1,1-dicarbonitriles in 30–60% yields.
Cite: Vereshchagin A.N. , Elinson M.N. , Feducovich S.K. , Zaimovskaya T.A. , Starikova Z.A. , Belyakov P.A. , Nikishin G.I.
A novel strategy of constructing the cyclohexane ring: stereoselective multicomponent cyclization of aromatic aldehydes, malononitrile, and acetone into cis-2,6-diaryl-4-dicyanomethylidenecyclohexane-1,1-dicarbonitriles
Russian Chemical Bulletin. 2008. V.57. N3. P.585-590. DOI: 10.1007/s11172-008-0091-y WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000263566900021
Scopus: 2-s2.0-62249150811
OpenAlex: W2181260734
Citing:
DB Citing
OpenAlex 3
Scopus 1
Web of science 1
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