4.8 Article

Direct Catalytic Asymmetric Reductive Amination of Aliphatic Ketones Utilizing Diphenylmethanamine as Coupling Partner

Journal

ORGANIC LETTERS
Volume 19, Issue 8, Pages 1942-1945

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b00212

Keywords

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Funding

  1. National Natural Science Foundation of China [21402155]
  2. Yangling Bureau of Science Technology [2016NY-25]
  3. Northwest AF University [Z109021521]

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The highly efficient direct catalytic reductive amination of ketones with diphenylmethanamine catalyzed by iridium-phosphoramidite complexes is described. As an effective coupling partner, diphenylmethanamine is suitable for a wide range of ketones to provide chiral amines in high yields and enantioselectivity. The chiral monodentate phosphoramidite ligands are tunable and competent to accommodate substrates with different structures.

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