Asymmetric Synthesis of Axially Chiral Arylpyrazole via an Organocatalytic Arylation Reaction

被引:11
|
作者
Gao, Xi [1 ]
Li, Chengwen [1 ]
Chen, Li [1 ,2 ]
Li, Xin [1 ,2 ]
机构
[1] Nankai Univ, Coll Chem, State Key Lab Elemento Organ Chem, Tianjin 300071, Peoples R China
[2] Haihe Lab Sustainable Chem Transformat, Tianjin 300192, Peoples R China
基金
中国国家自然科学基金;
关键词
ENANTIOSELECTIVE SYNTHESIS; ATROPOSELECTIVE SYNTHESIS; BRONSTED ACID; BIARYLS; ATROPISOMERS;
D O I
10.1021/acs.orglett.3c02694
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Herein, a highly enantioselective arylation reaction of 3-aryl-5-aminopyrazoles and quinone derivatives was realized using a chiral phosphoric acid catalyst under mild conditions. The reaction has a broad scope with respect to both arylation reaction partners and hence offers rapid access to an array of axially chiral arylpyrazoles with pretty outcomes (up to 95% yield and 99% ee). Notably, the reaction is very efficient, as the catalyst loadings for the model reaction can be reduced to 1 mol % and the enantioselectivity is still maintained. Besides, the synthetic utility of the protocol was proven by a gram-scale reaction and the transformation of the product.
引用
收藏
页码:7628 / 7632
页数:5
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