Simple manganese carbonyl catalyzed hydrogenation of quinolines and imines
Simple manganese carbonyl catalyzed hydrogenation of quinolines and imines作者机构:Beijing National Laboratory for Molecular SciencesCAS Key Laboratory of Molecular Recognition and FunctionCAS Research/Education Center for Excellence in Molecular SciencesInstitute of ChemistryChinese Academy of SciencesBeijing 100190China University of Chinese Academy of SciencesBeijing 100049China Provincial Key Laboratory of Oil&Gas Chemical TechnologyCollege of Chemistry and Chemical EngineeringNortheast Petroleum UniversityDaqing 163318China Physical Science LaboratoryHuairou National Comprehensive Science CenterBeijing 101400China
出 版 物:《Chinese Chemical Letters》 (中国化学快报(英文版))
年 卷 期:2020年第31卷第7期
页 面:1890-1894页
核心收录:
学科分类:081704[工学-应用化学] 07[理学] 08[工学] 0817[工学-化学工程与技术] 070303[理学-有机化学] 0703[理学-化学]
基 金:the National Natural Science Foundation of China(No.21772202,21831008) Beijing Municipal Science&Technology Commission(No.Z191100007219009) Beijing National Laboratory for Molecular Sciences(No.BNLMS-CXXM201901)
主 题:Manganese Hydrogenation Quinolines Imines Homogeneous catalysis
摘 要:Manganese-catalyzed hydrogenation of unsaturated molecules has made tremendous progresses recently benefiting from non-innocent pincer or bidentate ligands for ***,we describe the hydrogenation of quinolines and imines catalyzed by simple manganese carbonyls,Mn2(CO)10 or MnBr(CO)5,thus eliminating the prerequisite pincer-type or bidentate ligands.