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      Synthesis of tertiary amines by direct Brønsted acid catalyzed reductive amination.

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          Abstract

          Tertiary amines are ubiquitous and valuable compounds in synthetic chemistry, with a wide range of applications in organocatalysis, organometallic complexes, biological processes and pharmaceutical chemistry. One of the most frequently used pathways to synthesize tertiary amines is the reductive amination reaction of carbonyl compounds. Despite developments of numerous new reductive amination methods in the past few decades, this reaction generally requires non-atom-economic processes with harsh conditions and toxic transition-metal catalysts. Herein, we report simple yet practical protocols using triflic acid as a catalyst to efficiently promote the direct reductive amination reactions of carbonyl compounds on a broad range of substrates. Applications of this new method to generate valuable heterocyclic frameworks and polyamines are also included.

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          Author and article information

          Journal
          Chem Commun (Camb)
          Chemical communications (Cambridge, England)
          Royal Society of Chemistry (RSC)
          1364-548X
          1359-7345
          Aug 07 2020
          : 56
          : 61
          Affiliations
          [1 ] School of Chemistry, University of New South Wales, Sydney, Australia. t.v.nguyen@unsw.edu.au.
          Article
          10.1039/d0cc02955f
          32613957
          a706397b-b2f6-49bc-afad-1db5bfd3daae
          History

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