The E and Z isomers of 1-acetonaphthone oxime are isolated, characterized, and subjected to catalytic asymmetric hydrogenation; the chiral products from the asymmetric hydrogenation reflect the effect of the E and Z isomers on the enantioselectivity of the reaction.
A. S. C. Chan, C. Chen, C. Lin, Y. Lin, M. Cheng and S. Peng, J. Chem. Soc., Chem. Commun., 1995, 1767 DOI: 10.1039/C39950001767
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