@article {35407,
	title = {A highly active organocatalyst for the asymmetric alpha-aminoxylation of aldehydes and alpha-hydroxylation of ketones},
	journal = {RSC AdvancesRSC Advances},
	volume = {2},
	number = {15},
	year = {2012},
	note = {971PPTimes Cited:3Cited References Count:36},
	pages = {6164-6166},
	abstract = {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.},
	keywords = {aldol, amino-acid, aminocatalysis, carbonyl-compounds, catalysis, chemistry, derivatives, mannich, proline, sulfonamide},
	isbn = {2046-2069},
	author = {Fan, X. Y. and Alza, E. and Pericas, M. A.}
}
