Chelating 1,2-Bis(2′-picolyl)-o-carborane as a Supporting Ligand for Pd-Catalyzed Selective B(3,6)-H Difunctionalization of o-Carboranes

被引:0
作者
Ma, Qiang-Qiang [1 ,2 ]
Zhou, Peng [1 ,2 ]
Liu, Yizhen [1 ,2 ]
Xie, Zuowei [1 ,2 ]
机构
[1] Southern Univ Sci & Technol, Shenzhen Grubbs Inst, Shenzhen 518055, Guangdong, Peoples R China
[2] Southern Univ Sci & Technol, Dept Chem, Shenzhen 518055, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
FORMING REDUCTIVE ELIMINATION; HYPERVALENT IODINE(III) REAGENTS; B-H ACTIVATION; OXIDATIVE ADDITION; BORON CLUSTERS; C-O; PALLADIUM; COMPLEXES; ARYL; REACTIVITY;
D O I
10.1021/acs.inorgchem.5c00383
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Transition metal catalyzed selective cage B-H functionalization of carboranes has made significant progress in recent years, giving rise to the efficient synthesis of a large variety of cage B-functionalized carboranes including alkenylation, arylation, alkynylation, borylation, hydroxylation, acyloxylation, amination, and halogenation. However, the mechanisms of these catalytic B-X coupling reactions are not well understood. Herein, we describe the isolation and characterization of the catalytically relevant o-carborane based palladium(II) metallacycle, disclosing the details of Pd-catalyzed B-H functionalization of o-carboranes. As a result, highly selective catalytic B(3,6)-dihalogenation, -dimethylation, and -diarylation of o-carboranes have been achieved.
引用
收藏
页码:5707 / 5715
页数:9
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