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Lanthanide Amide-catalyzed Aza-Henry Reaction of N-Tosyl Imines with Nitroalkanes
Authors:ZHANG  Lijun  WU  Hongping  SU  Shunpeng  WANG  Shaowu
Institution:Anhui Key Laboratory of Functional Molecular Solids,Institute of Organic Chemistry,School of Chemistry and Materials Science,Anhui Normal University,Wuhu,Anhui 241000,China
Abstract:In the presence of 10 mol% lanthanide amide (Me3Si)2N]3Ln(µ‐Cl)Li(THF)3, the aza‐Henry reaction of N‐tosyl imines with nitroalkanes (1:5 molar ratio) could be performed in good yields. The lanthanide amide‐catalyzed aza‐Henry reaction has the features of mild reaction conditions, tolerance of a variety of aromatic aldehyde‐derived imines and nitroalkanes, short time and good chemical yields. A catalytic mechanism for the reaction was also proposed.
Keywords:lanthanide amide  aza-Henry reaction  N-tosyl imine  nitroalkane  catalysis
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