Highly Selective Hydroboration of Alkenes, Ketones and Aldehydes Catalyzed by a Well-Defined Manganese Complex

被引:163
作者
Zhang, Guoqi [1 ,2 ]
Zeng, Haisu [1 ,2 ,3 ]
Wu, Jing [1 ,2 ,3 ]
Yin, Zhiwei [1 ,2 ,3 ]
Zheng, Shengping [3 ]
Fettinger, James C. [4 ]
机构
[1] CUNY, John Jay Coll, Dept Sci, New York, NY 10019 USA
[2] CUNY, PhD Chem Program, Grad Ctr, New York, NY 10019 USA
[3] CUNY, Hunter Coll, Dept Chem, New York, NY 10065 USA
[4] Univ Calif Davis, Dept Chem, Davis, CA 95616 USA
基金
美国国家科学基金会;
关键词
alkenes; carbonyl compounds; hydroboration; manganese catalysis; Markovnikov selectivity; CROSS-COUPLING REACTIONS; ASYMMETRIC HYDROBORATION; ISOMERIZATION-HYDROBORATION; GRIGNARD-REAGENTS; COBALT CATALYSTS; HYDROSILYLATION; REDUCTION; LIGAND; REGIO; CHEMO;
D O I
10.1002/anie.201607579
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Well-defined manganese complexes based on inexpensive, readily available ligands, 2,2': 6', 2 ''-terpyridine and its derivatives have been prepared and employed for the selective hydroboration of alkenes, ketones and aldehydes. Highly Markovnikov regioselective hydroboration of styrenes as well as excellent chemoselective hydroboration of ketones over alkenes were achieved, for the first time, by an earth-abundant manganese catalyst.
引用
收藏
页码:14367 / 14370
页数:4
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