4.6 Article

A highly active organocatalyst for the asymmetric α-aminoxylation of aldehydes and α-hydroxylation of ketones

Journal

RSC ADVANCES
Volume 2, Issue 15, Pages 6164-6166

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2ra20968c

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Funding

  1. MINECO [CTQ2008-00947/BQU]
  2. DEC [2009SGR623]
  3. ICIQ Foundation

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Enantiopure trans-3-trifluoromethylsulfonylamino-4-silyloxypyrrolidines efficiently catalyse the asymmetric alpha-aminoxylation of aldehydes. At 1% catalyst loading (solvent-free conditions) or at 2% catalyst loading (acetonitrile solution) aldehydes are completely converted in short reaction times leading to alpha-aminoxylation products with very high (96-99%) enantioselectivity.

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