Electrochemical transformation of cyanoacetic ester and alkylidenecyanoacetic esters into 3-substituted 1,2-dicyanocyclopropane-1,2-dicarboxylates
作者:M. N. Elinson、S. K. Feducovich、S. G. Bushuev、D. V. Pashchenko、G. I. Nikishin
DOI:10.1007/bf02503485
日期:1998.6
Electrolysis of cyanoaceticester and alkylidenecyanoacetic esters in an undivided cell in the presence of mediators (alkali metal halides) gives rise to 3-substituted, 1,2-dicyanocyclopropane-1,2-dicarboxylates in 60–95% yields.
Reactions of a Tetrasubstituted Thiocarbonyl Ylide; New Evidence for Two-Step Cycloadditions
作者:Rolf Huisgen、Grzegorz Mloston
DOI:10.3987/com-89-s40
日期:——
Electrochemical conversions of alkyl alkylidenecyanoacetates into 3-substituted dialkyl 1,2-dicyanocyclopropane-1,2-dicarboxylates
作者:M. N. Elinson、S. K. Feducovich、T. L. Lizunova、G. I. Nikishin
DOI:10.1007/bf02496405
日期:1999.8
Electrolysis of alkyl alkylidenecyanoacetates in an undivided cell in the presence of alkali metal halides as mediators afforded 3-substituted dialkyl 1,2-dicyanocyclopropane-1,2-dicarboxylates in 50-85% yields.