A supramolecularly tunable chiral diphosphine ligand: application to Rh and Ir-catalyzed enantioselective hydrogenation

被引:34
作者
Zhang, Xi-Chang [1 ,2 ]
Hu, Yi-Hu [1 ]
Chen, Chuan-Fu [1 ]
Fang, Qiang [1 ]
Yang, Li-Yao [1 ]
Lu, Ying-Bo [1 ]
Xie, Lin-Jie [1 ]
Wu, Jing [1 ]
Li, Shijun [1 ]
Fang, Wenjun [2 ]
机构
[1] Hangzhou Normal Univ, Coll Mat Chem & Chem Engn, Hangzhou, Zhejiang, Peoples R China
[2] Zhejiang Univ, Dept Chem, Hangzhou 310003, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
ASYMMETRIC HYDROGENATION; P-PHOS; COPPER(II)-DIPYRIDYLPHOSPHINE CATALYST; DIPYRIDYLPHOSPHINE LIGANDS; HETEROAROMATIC-COMPOUNDS; HOMOGENEOUS CATALYSIS; ISOQUINOLINIUM SALTS; PHOSPHORUS LIGANDS; IRIDIUM COMPLEXES; BIDENTATE LIGANDS;
D O I
10.1039/c6sc00589f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A supramolecularly tunable chiral bisphosphine ligand bearing two pyridyl-containing crown ethers, (-) or (+)-Xyl-P16C6-Phos, was fabricated and utilized in the Rh-catalyzed asymmetric hydrogenation of alpha-dehydroamino acid esters and Ir-catalyzed asymmetric hydrogenation of quinolines in high yields with excellent enantioselectivities (90-99% ee). Up to a 22% enhancement in enantioselectivity was achieved by the addition of certain amounts of alkali ions (Li+, Na+ or K+), which could be selectively recognized and effectively complexed by the crown ethers on the chiral Xyl-P16C6-Phos.
引用
收藏
页码:4594 / 4599
页数:6
相关论文
共 78 条
[1]   Rhodium-catalyzed hydroformylation of alkynes employing a self-assembling ligand system [J].
Agabekov, Vladislav ;
Seiche, Wolfgang ;
Breit, Bernhard .
CHEMICAL SCIENCE, 2013, 4 (06) :2418-2422
[2]  
[Anonymous], 2010, CATALYTIC ASYMMETRIC
[3]  
Barton D., 1999, Comprehensive Natural Products Chemistry, V1
[4]   Supramolecular Encapsulated Rhodium Catalysts for Branched Selective Hydroformylation of Alkenes at High Temperature [J].
Besset, Tatiana ;
Norman, David W. ;
Reek, Joost N. H. .
ADVANCED SYNTHESIS & CATALYSIS, 2013, 355 (2-3) :348-352
[5]   HETEROAROMATICITY .5. A UNIFIED AROMATICITY INDEX [J].
BIRD, CW .
TETRAHEDRON, 1992, 48 (02) :335-340
[6]   Artificial switchable catalysts [J].
Blanco, Victor ;
Leigh, David A. ;
Marcos, Vanesa .
CHEMICAL SOCIETY REVIEWS, 2015, 44 (15) :5341-5370
[7]   A Switchable [2]Rotaxane Asymmetric Organocatalyst That Utilizes an Acyclic Chiral Secondary Amine [J].
Blanco, Victor ;
Leigh, David A. ;
Marcos, Vanesa ;
Morales-Serna, Jose A. ;
Nussbaumer, Alina L. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2014, 136 (13) :4905-4908
[8]   A Rotaxane-Based Switchable Organocatalyst [J].
Blanco, Victor ;
Carlone, Armando ;
Haenni, Kevin D. ;
Leigh, David A. ;
Lewandowski, Bartosz .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2012, 51 (21) :5166-5169
[9]   Supramolecular approaches to generate libraries of chelating bidentate ligands for homogeneous catalysis [J].
Breit, B .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (42) :6816-6825
[10]   Hydrogen bonding as a construction element for bidentate donor ligands in homogeneous catalysis: Regioselective hydroformylation of terminal alkenes [J].
Breit, B ;
Seiche, W .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (22) :6608-6609