Journal of Organic Chemistry p. 1383 - 1389 (1986)
Update date:2022-08-05
Topics:
Coates, Robert M.
Cummins, Clark H.
Acylation-rearrangement of N-tert-butyl and N-cyclohexyl nitrones of cyclohexanecarboxaldehyde (1), n-butyraldehyde, isobutyraldehyde, 3-cyclohexenecarboxaldehyde, and α-methylpropionaldehyde gave α-pivaloyloxy imines, which underwent reduction with lithi
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