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

Enantiopure trans-3-trifluoromethylsulfonylamino-4-silyloxypyrrolidines efficiently catalyse the asymmetric α-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 α-aminoxylation products with very high (96-99%) enantioselectivity.

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

X. Fan, E. Alza, M. A. Pericàs

RSC Adv. 2012, 2, 6164-6166
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