TABLE 1

Summary of the specific rotation and enantiomeric excess of α-OHTAM stereoisomers

Values of ee were determined by the formation of the α-camphanate ester of each enantiomer and evaluation of 1H NMR spectra of the esters.


α-OHTAM

[α]D25

ee
%
E-(+)-α-OHTAM +110.7 99
E-(-)-α-OHTAM -94.7 85
Z-(+)-α-OHTAM +77.1 92
Z-(-)-α-OHTAM
-74.5
90