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(S)-3-(4-Fluoro-2-methylphenyl)piperazin-2-one synthesis

2synthesis methods
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Yield:56 % ee

Reaction Conditions:

with C37H42IrNOPRu(1+)*C32H12BF24(1-);hydrogen in dichloromethane at 20; under 52505.3 Torr; for 72 h;Autoclave;Overall yield = 72 %; enantioselective reaction;

References:

Wang, Yanzhao;Liu, Yuanyuan;Li, Kun;Yang, Guoqiang;Zhang, Wanbin [Advanced Synthesis and Catalysis,2017,vol. 359,# 11,p. 1933 - 1941] Location in patent:supporting information