Enantioselective hydrogenation of N-heteroaromatics catalyzed by chiral diphosphine modified binaphthyl palladium nanoparticles

被引:22
|
作者
Xia, Yun-Tao [1 ,2 ]
Ma, Jing [1 ,2 ]
Wang, Xiao-Dong [1 ,2 ]
Yang, Lei [1 ,2 ]
Wu, Lei [1 ,2 ,3 ]
机构
[1] Nanjing Agr Univ, Jiangsu Key Lab Pesticide Sci, Coll Sci, Nanjing 210095, Jiangsu, Peoples R China
[2] Nanjing Agr Univ, Dept Chem, Coll Sci, Nanjing 210095, Jiangsu, Peoples R China
[3] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Inst Chem, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
DENDRIMER-ENCAPSULATED NANOPARTICLES; ASYMMETRIC HYDROGENATION; NITROGEN-HETEROCYCLES; COUPLING REACTIONS; ARYLBORONIC ACIDS; CHEMOSELECTIVE REDUCTION; RECYCLABLE CATALYSTS; METAL NANOPARTICLES; GOLD NANOPARTICLES; ROOM-TEMPERATURE;
D O I
10.1039/c7cy01672g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The first application of binaphthyl-stabilized palladium nanoparticles (Bin-PdNPs) with chiral modifiers in asymmetric hydrogenation of N-heteroaromatics is revealed. With an appropriate ratio of R-BINAP/Bin-PdNPs used, the pre-prepared chiral nanocatalyst achieves asymmetric hydrogenations of 2-substituted quinolines with good to excellent yields and moderate enantioselectivities, which showed superior catalytic properties to the R-BINAP/Pd complex. Moreover, this protocol is also applicable to 2-substituted indoles.
引用
收藏
页码:5515 / 5520
页数:6
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