55330-47-7Relevant academic research and scientific papers
Acid-promoted rapid solvent-free access to substituted 1,4-dihydropyridines from β-ketothioamides
Li, Ming,Sun, Ke-Na,Wen, Li-Rong
, p. 21535 - 21539 (2016/03/08)
β-Ketothioamides (KTAs) have been used as building blocks with aldehydes and β-enaminonitriles for synthesis of 1,4-dihydropyridines in the presence of AcOH under solvent-free conditions within 5 min. This new strategy exhibits remarkable features such as high chemoselectivity, mild reaction conditions, easily available substrates, and good yields.
Highly efficient RhI-catalyzed asymmetric hydrogenation of β-amino acrylonitriles
Ma, Miaofeng,Hou, Guohua,Sun, Tian,Zhang, Xiaowei,Li, Wei,Wang, Junru,Zhang, Xumu
supporting information; experimental part, p. 5301 - 5304 (2010/09/08)
(Figure Presented) It takes two to TangPhos: β-Amino acrylonitriles can be readily prepared from acetonitriles. Both of the E/Z isomers undergo hydrogenation with excellent enantioselectivity by using the Rh-TangPhos (TangPhos = l, 1'-ditert-butyl-(2, 2')-diphospholane) catalyst system. The products, chiral β-amino nitriles, are valuable chiral building blocks for many drugs.
β Aminocinnamonitriles as potential antiinflammatory agents
Lang Jr.,Cohen
, p. 441 - 443 (2007/10/08)
A number of β aminocinnamonitriles have been prepared by the reaction of salts of acetonitrile and proprionitrile with benzonitrile. These materials were evaluated in the carrageenan antiinflammatory screen in Royal Hart, Wistar strain rats. Despite food weight gains with the parent molecule, β aminocinnamonitrile, only marginal activity was found in related compounds and some possible 'metabolites'.
