Abstract
The intramolecular reactivity of a nitrone derived from 2-(cyclohexen-3-yloxy)benzaldehyde has been investigated. By using ( R)- α-phenylethylamine as chiral auxiliary, enantiomerically pure (9-amino-substituted) 1,2,3,4,4a,9a-hexahydro-9 H-xanthen-1-ols were produced in satisfactory way.
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