Elliot Coulbeck, Marco Dingjan, J. Eames*
Apr 30, 2009
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Journal
Chirality
Abstract
The parallel kinetic resolution of racemic 2-aryl-2-deuterio-propionic and butanoic acids using an equimolar combination of quasi-enantiomeric oxazolidin-2-ones is discussed. The levels of diastereoselectivity were high leading to enantiomerically pure D-labeled products in good yield.