71908-64-0Relevant academic research and scientific papers
Imidazole-mediated cascade [2 + 2 + 2] annulation reactions: A highly diastereoselective synthetic protocol for the construction of multiply substituted cyclohexanes
Liu, Xu-Guang,Shi, Min
scheme or table, p. 6168 - 6174 (2009/05/27)
A novel imidazole-mediated [2 + 2 + 2] annulation process that enables the diastereoselective synthesis of multiply substituted cyclohexanes 3 in a one-pot, three-component manner from two units of (arylmethylidene) malononitriles 1 and one unit of nitroalkenes 2 is described. These cyclohexane derivatives were obtained in moderate to good yields under mild conditions. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.
SYNTHESIS AND CHEMICAL REACTIVITY OF 4,4-DISUBSTITUTED PYRANAMINES
Martin-Leon, Nazario,Segura, Jose L.,Seoane, Carlos,Soto, Jose L.
, p. 2434 - 2452 (2007/10/02)
The synthesis of a variety of 4,4-disubstituted 4H-pyranamines from alkylarylpropenenitriles and benzoylacetonitrile is reported.The reaction requirements demanded a different approach from the general synthesis of 2-amino-4H-pyrans.Electronic and steric
DIMERIZATION OF 2-ARYLPROPENE-1,1-DICARBONITRILES
Abramenko, Yu. T.,Ivashchenko, A. V.,Nogaeva, K. A.,Andronova, N. A.,Putsykina, E. B.
, p. 230 - 235 (2007/10/02)
The base-catalyzed dimerization of 2-arylpropene-1,1-dicarbonitriles to 2-amino-4,6-diaryl-5-methyl-2,4-cyclohexadiene-1,1,3-tricarbonitriles and also the recyclization of the latter to 4,6-diaryl-6-methyl-2-dicyanomethylene-1,2,5,6-tetrahydronicotinonitr
