Journal of the Chemical Society. Chemical communications p. 1767 - 1768 (1995)
Update date:2022-08-16
Topics:
Chan, Albert S. C.
Chen, Chih-Chiang
Lin, Ching-Wen
Lin, Ying-Chih
Cheng, Ming-Chu
Peng, Shie-Ming
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.
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