524036-75-7Relevant academic research and scientific papers
Electrocatalytic multicomponent cyclization of an aldehyde, malononitrile and a malonate into 3-substituted-2,2-dicyanocyclopropane-1,1-dicarboxylate-the first one-pot synthesis of a cyclopropane ring from three different molecules
Elinson, Michail N.,Feducovich, Sergey K.,Vereshchagin, Anatolii N.,Gorbunov, Sergey V.,Belyakov, Pavel A.,Nikishin, Gennady I.
, p. 9129 - 9133 (2006)
Electrolysis of an aldehyde, malononitrile and a malonate in an alcohol in an undivided cell in the presence of sodium acetate-sodium halide as a double mediatory system results in the formation of 3-substituted-2,2-dicyanocyclopropane-1,1-dicarboxylates
Electrocatalytic multicomponent cyclization of aromatic aldehydes, malononitrile, and malonates into 3-substituted 2,2-dicyanocyclopropane-1,1- dicarboxylates
Vereshchagin,Elinson,Dorofeev,Nikishin
experimental part, p. 902 - 907 (2010/10/04)
Electrolysis of aromatic aldehydes, malononitrile and malonates in methanol in an undivided cell in the presence of double-mediator system NaBr-NaOAc afforded 3-substi-tuted 2,2-dicyanocyclopropane-1,1-dicarboxylates in 40-60% yields.
Electrocatalytic transformation of dialkyl malonates and arylidene- or alkylidenemalononitriles into dialkyl esters of 3-substituted 2,2-dicyanocyclopropane-1,1-dicarboxylic acids
Elinson,Feducovich,Zaimovskaya,Vereshchagin,Gorbunov,Nikishin
, p. 1593 - 1598 (2007/10/03)
Electrolysis of alcoholic solutions of dialkyl malonates and arylidene- or alkylidenemalononitriles in the presence of NaBr in an undivided cell gave dialkyl esters of 3-substituted 2,2-dicyanocyclopropane-1,1-dicarboxylic acids in 60-90% yields.
