
%0 Journal Article
%A Bell, KH 
%T Prediction of the Absolute Configurations of the Enantiomers of Racemic Primary and Secondary Alcohols and Primary Amines by Kinetic Resolution with (2R,3R)-2,3-Diacetoxysuccinic Anhydride
%J Australian Journal of Chemistry
%D 1979/12/01
%V 32
%N 12
%P 2625-2629
%K 
%R https://doi.org/10.1071/CH9792625
%U https://www.publish.csiro.au/paper/CH9792625 
%X The absolute configurations of the enantiomers of a variety of racemic secondary and primary alcohols and racemic primary amines have been correctly predicted from the results of kinetic resolution with (2R,3R)-2,3-diacetoxysuccinic anhydride. In the prediction model (1), allocation of relative sizes to the groups attached to the chiral centre was based on conformational free energy differences. 
