Acylation-rearrangement of N-tert-butyl and N-cyclohexyl nitrones of cyclohexanecarboxaldehyde (l), nbutyraldehyde, isobutyraldehyde, 3- cyclbhexenecarboxaldehyde, and a-methylpropionaldehyde gave cy-pivaloyloxy imiies, which underwent reduction with lithium aluminum hydridit to N-tert-butyl-and N- cyclohexylamino alcohols (Table I). Reduction of the cy-pivaloyloxy imines derived from 1 ...