Chiral Ferrocenyl N,N Ligands with Intramolecular Hydrogen Bonds for Highly Enantioselective Allylic Alkylations

被引:13
|
作者
Yao, Lin [1 ]
Nie, Huifang [1 ]
Zhang, Dongxu [1 ]
Wang, Libin [1 ]
Zhang, Yuhao [1 ]
Chen, Weiping [1 ]
Li, Zhenhua [2 ]
Liu, Xueying [1 ]
Zhang, Shengyong [1 ]
机构
[1] Fourth Mil Med Univ, Sch Pharm, Dept Med Chem, 169 Changle West Rd, Xian 710032, Shaanxi, Peoples R China
[2] Fudan Univ, Shanghai Key Lab Mol Catalysis & Innovat Mat, Dept Chem, 220 Handan Rd, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
alkylation; asymmetric catalysis; hydrogen bonds; N-ligands; palladium; OXAZOLINE-CONTAINING LIGANDS; SUBSTITUTED CINNAMIC-ACIDS; CHENPHOS-RH COMPLEX; ASYMMETRIC CATALYSIS; BIS(OXAZOLINE) LIGANDS; PHOSPHINE-LIGANDS; THIOUREA ORGANOCATALYSTS; DIPHOSPHINE LIGANDS; AROMATIC-ALDEHYDES; CARBONYL-COMPOUNDS;
D O I
10.1002/cctc.201701461
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
Several new ferrocene-derived bidentate N ligands, which contain multiple chiral factors, have been designed and synthesized by a rational combination of oxazoline and pyridine. Their catalytic performances were investigated preliminarily in Pd-catalyzed asymmetric allylic alkylation, and excellent reactivities and enantioselectivities (up to 99% yield and 98% ee) were realized if we used the ligand with a matched chirality. DFT calculations were used to illustrate that an intramolecular hydrogen bond formed between the hydroxyl group and the oxazoline fragment of the ligand contributed to the optimal conformation of the ligand-Pd-allyl complex.
引用
收藏
页码:804 / 809
页数:6
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