脱氢
催化作用
化学
氧化磷酸化
环境友好型
铜
化学计量学
组合化学
有机化学
生态学
生物化学
生物
作者
Yue Ji,Ze‐Lin Dang,Xuemei Liu,Ben Niu,Weiwei Han,Taotao Qiang,Sichang Wang
标识
DOI:10.1002/slct.202301863
摘要
Abstract An efficient copper‐catalyzed oxidative dehydrogenation of tetrahydroisoquinolines has been developed, giving a general and convenient strategy from amines toward imines in excellent yields. A series of tetrahydroisoquinolines bearing electron‐donating/withdrawing groups proceeded smoothly with air (O 2 ) as oxidant. The oxidative dehydrogenation proved to be an atom‐economical and environmentally friendly strategy, which could effectively avoid generating stoichiometric hazardous wastes. In addition, this methodology provides a convenient and effective approach to the reutilization of amines, especially for the synthesis of enantiomerically pure substances, such as (+)‐Solifenacin, in industrial process. Preliminary experimental results revealed that the reaction was carried out via a process of oxidative dehydrogenation.
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