17424-71-4Relevant academic research and scientific papers
Organometallic hollow spheres bearing bis(N-Heterocyclic carbene)-palladium species: Catalytic application in three-component Strecker reactions
Choi, Jaewon,Yang, Hye Yun,Kim, Hae Jin,Son, Seung Uk
, p. 7718 - 7722 (2010)
Hollow-sphere catalysts were prepared by means of 3D network formation between a tetraimidazolium building block and palladium acetate. The bis(N-heterocyclic carbene)-palladium species that were concomitantly formed during growth of the hollow spheres sh
Highly efficient three-component Strecker-type reaction catalyzed by MgI2 etherate under solvent-free conditions
Li, Pengcheng,Zhang, Yongdong,Chen, Zhili,Zhang, Xingxian
supporting information, p. 1854 - 1858 (2017/04/21)
A concise, straightforward and efficient method has been developed for the synthesis of α-aminonitriles by an one-pot three-component condensation of aldehydes or ketones, amines and trimethylsilyl cyanide catalyzed by MgI2 etherate under solvent-free conditions. This protocol has some advantages such as mild reaction condition, simple work-up, short reaction time and high product yields.
Sulfated tungstate: A green catalyst for Strecker reaction
Pathare, Sagar P.,Akamanchi, Krishnacharya G.
experimental part, p. 871 - 875 (2012/03/08)
A straightforward, mild, efficient, and general method has been developed for the synthesis of α-aminonitriles via Strecker reaction starting from aldehydes or ketones, amines, and trimethylsilyl cyanide in the presence of sulfated tungstate as a heterogeneous mild solid acid catalyst at room temperature and solvent free condition. The developed method has been successfully applied for the synthesis of a wide range of α-aminonitriles with variable functionality.
Synthesis and reactions of 4-hydroxy-2(1H)-pyridones with thienyl and pyridyl substituents in position 6 starting with azomethines and malonates
Schnell, Barbara
, p. 541 - 548 (2007/10/03)
The reaction of 4 with substituted diethyl malonates 5a, or 'magic malonates' (bis-2,4,6-trichlorophenylmalonates 5b) leads to 4-hydroxy-2(1H)- pyridones 6. The azomethines 4 are prepared via the Strecker compounds 3 starting with methyl ketones 1, anilines, and potassium cyanide. Chlorination of pyridones 6 with sulfuryl chloride leads to compounds 7 while nitration gives 9.
