Muller, T.E., Hultzsch, K.C., Yus, M., Foubelo, F. and Tada, M. (2008) Hydroamination: Direct Addition of Amines to Alkenes and Alkynes. Chemical Reviews, 108, 3795-3892.
http://dx.doi.org/10.1021/cr0306788

has been cited by the following article:

• TITLE: Preparation of 2,5-Bis(Aminomethyl)Furan by Direct Reductive Amination of 2,5-Diformylfuran over Nickel-Raney Catalysts

  AUTHORS: Ngoc-Thuc Le, Areum Byun, Yohan Han, Kee-In Lee, Hyungrok Kim

  KEYWORDS: Reductive Amination, Primary Amine, 2, 5-Bis(Aminomethyl)Furan, 2, 5-Diformylfuran, Nickel Raney Catalyst

  JOURNAL NAME: Green and Sustainable Chemistry, Vol.5 No.3, August 5, 2015

  ABSTRACT: The direct reductive amination of 2,5-diformylfuran (DFF) with ammonia to 2,5-bis(aminomethyl)furan (BAF) was demonstrated, for the first time, over the commercial type Nickel-Raney and acid treated Nickel-Raney catalysts. The effects of reaction parameters such as reaction medium, temperature and hydrogen pressure were described. The acid treated Nickel-Raney catalyst exhibited the highest BAF yield in the THF-water mixed reaction medium. The relatively higher Ni0 species composition and larger surface area of the acid treated Nickel-Raney catalyst with specific reaction conditions contributed greatly to the BAF formation. The oligomeric species, such as furanic imine trimers and tetramers confirmed by MALDI-MS analysis were presented as the intermediates of DFF reductive amination.