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作 者:Qinli Lu Xianming Wang Wanliu Wen Ruifeng Fan Binfeng Zhu Bingjie Zhou Jingchao Chen Baomin Fan
机构地区:[1]Key Laboratory of Chemistry in Ethnic Medicinal Resources(Yunnan Minzu University),State Ethnic Affairs Commission&Ministry of Education,Yunnan Minzu University,Kunming,650500,China [2]Department School of Chemistry and Environment,Yunnan Minzu University,Kunming 650500,China [3]School of Pharmaceutical Science&Yunnan Key Laboratory of Pharmacology for Natural Products,Kunming Medical University,Kunming 650500,China
出 处:《Green Synthesis and Catalysis》2024年第3期175-179,共5页绿色合成与催化(英文)
基 金:grateful to the National Natural Science Foundation of China(Nos.21961045 and 22061048);the Basic Research Project of Chongqing Academy of Chinese Materia Medica(No.jbky20190028);the Fund Project of Yunnan Key Laboratory of Pharmacology for Natural Products(No.YKLPNP-K2303);Yunnan Provincial Key Laboratory Construction Plan Funding of Universities;Yunnan Provincial Engineering Research Center Construction Plan Funding of Universities for their financial support.
摘 要:The nitrile compounds are present in a variety of biologically active natural products and pharmaceuticals,and the nitrile groups are versatile synthetic intermediates to other functionalized compounds.Herein,the asymmetric reduction ofα,β-unsaturated nitriles with water as a hydrogen source is reported.The reaction is catalyzed by the complex of[Ir(COD)Cl]_(2)and(R_(a),S)-Ph-Bn-SiPhox,and allows the preparation of useful enantioenriched chiral 3,3-disubstituted propionitriles with high optical purities in mild conditions.
关 键 词:Asymmetric reduction Unsaturated nitriles WATER PROPIONITRILE IRIDIUM DIBAL-H
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