77198-31-3Relevant academic research and scientific papers
An improved and clean procedure for the synthesis of one-donor poly-acceptors systems containing 2,6-dicyanoamine moiety in aqueous media catalyzed by TEBAC in the presence and absence of K2CO3
Wang, Xiang-Shan,Zhang, Mei-Mei,Li, Qing,Yao, Chang-Sheng,Tu, Shu-Jiang
, p. 5265 - 5273 (2007)
A clean and simple synthesis of one-donor poly-acceptors systems containing 2,6-dicyanoamine moiety was accomplished via the reaction of 1-arylethylidenemalonodinitriles with arylidenemalonodinitriles in aqueous media catalyzed by TEBAC in the presence of
Primary 1,2-diamine catalysis III: An unexpected domino reaction for the synthesis of multisubstituted cyclohexa-1,3-dienamines
Wang, Junfeng,Li, Qin,Qi, Chao,Liu, Yi,Ge, Zemei,Li, Runtao
supporting information; experimental part, p. 4240 - 4242 (2010/11/18)
The first organocatalyzed multicomponent domino reactions of aryl ketones, aldehydes and malononitrile were carried out successfully to afford multisubstituted cyclohexa-1,3-dienamines in satisfactory yields.
CYCLIZATION REACTIONS OF NITRILES. III. SYNTHESIS OF o-CYANOANILINES BY THE THORPE REACTION
Sharanin, Yu. A.,Baskakov, Yu. A.,Abramenko, Yu. T.,Putsykin, Yu. G.,Vasil'ev, A. F.,Nazarova, E.B.
, p. 1870 - 1879 (2007/10/02)
The reaction of alkylidenemalononitriles with arylidene derivatives of malononitrile and cyanoacetic ester leads to the formation of derivatives of 1-amino-2,6-dicyano-3,5-diaryl-1,3-cyclohexadiene or 2,4-dicyano-3-amino-5-arylbicyclodeca-2,10-dien
