作者：Paixao Mircio W; Nielsen Martin; Jacobsen Christian Borch; Jorgensen Karl Anker*
来源：Organic and Biomolecular Chemistry, 2008, 6(19): 3467-3470.
DOI：10.1039/b812369a
摘要
The organocatalytic ring-opening of N-tosyl protected aziridines by beta-ketoesters under chiral PTC-conditions, leading to the formation of optically active aminoethyl functionalised compounds with up to 99% ee, has been developed.
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