ENANTIOSELECTIVE HYDROGENATION OF (E)-ALPHA-PHENYLCINNAMIC ACID OVER CINCHONIDINE-MODIFIED PALLADIUM CATALYSTS

被引:62
作者
NITTA, Y
UEDA, Y
IMANAKA, T
机构
关键词
D O I
10.1246/cl.1994.1095
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Prochiral (E)-alpha-phenylcinnamic acid was hydrogenated enantioselectively over alumina- and titania-supported Pd catalysts modified with cinchonidine giving optical yields of 36.9% and 44.4%, respectively, in favor of (S)-(+)-2,3-diphenylpropionic acid. The influence of solvent on the optical yield was significant; a water containing solvent gave the best result.
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页码:1095 / 1098
页数:4
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