127722-99-0Relevant academic research and scientific papers
CYCLIZATION OF NITRILES XLII.SYNTHESIS, STRUCTURE AND STEREODEGENERATE TRANSFORMATION OF 1-AMINO-5-ARYL-2,6,6-TRICYANO-3-CYCLOPROPYL-1,3-CYCLOHEXADIENES
Sharanin, Yu. A.,Khoroshilov, G.E.,Shestopalov, A.M.,Nesterov, V.N.,Shklover, V.E.,Litvinov, V.P.
, p. 253 - 264 (2007/10/02)
The reaction of arylmethylenemalononitriles with (1-cyclopropylethylidene)malononitrile leads to 5-aryl-3-imino-2,4,4-tricyano-1-cyclopropyl-1-cyclohexanes, which are converted as a result of 1,5-sigmatropic rearangement into 1-amino-5-aryl-2,6,6-tricyano
SYNTHESIS, STRUCTURE, AND TRANSFORMATION OF 1-AMINO-5-PHENYL-2,6,6-TRICYANO-3-CYCLOPROPYL-1,3-CYCLOHEXADIENE INTO 6-PHENYL-2-DICYANOMETHYLENE-3-CYANO-4-CYCLOPROPYL-1,2-DIHYDROPYRIDINE
Nesterov, V. N.,Shklover, V. E.,Sharanin, Yu. A.,Struchkov, Yu. T.,Khoroshilov, G. E.
, p. 2541 - 2545 (2007/10/02)
1-Amino-5-phenyl-2,6,6-tricyano-3-cyclopropyl-1,3-cyclohexadiene is prepared by reaction of benzylidenemalononitrile with (1-cyclopropylethylidene)malononitrile.According to x-ray structural data, steric effects of the cyclohexadiene cause the C1/su
