Pd(<sc>ii</sc>)-Catalyzed enantioselective C-H olefination toward the synthesis of P-stereogenic phosphinamides

被引:6
作者
Chen, Zi-Jia [1 ]
Fan, Ling-Jie [2 ]
Xie, Pei-Pei [1 ]
Qian, Pu-Fan [1 ]
Hu, Xinquan [2 ]
Zhou, Tao [1 ,3 ]
Shi, Bing-Feng [1 ,3 ,4 ]
机构
[1] Zhejiang Univ, Ctr Chem Frontier Technol, Dept Chem, Hangzhou 310027, Peoples R China
[2] Zhejiang Univ Technol, Coll Chem Engn, Hangzhou 310032, Peoples R China
[3] Hangzhou Normal Univ, Coll Mat Chem & Chem Engn, Key Lab Organosilicon Chem & Mat Technol, Minist Educ, Hangzhou 311121, Zhejiang, Peoples R China
[4] Jiaxing Univ, Coll Biol Chem Sci & Engn, Jiaxing 314001, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
CATALYZED ASYMMETRIC PHOSPHINATION; SECONDARY PHOSPHINE; CHIRAL PHOSPHINES; BRONSTED ACID; FUNCTIONALIZATION; ACTIVATION; LIGANDS; C(SP(2))-H; ARYLATION; DESYMMETRIZATION;
D O I
10.1039/d3cc05052a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
P-Stereogenic phosphorus compounds are important structural elements in chiral ligands or organocatalysts. Herein, we report a Pd(ii)-catalyzed enantioselective C-H olefination toward the synthesis of P-stereogenic phosphinamides using cheap commercially available l-pGlu-OH as a chiral ligand. A broad range of P-stereogenic phosphinamides were gained in good yields with high enantioselectivities (33 examples, up to 77% yield, 99% ee) via desymmetrization and kinetic resolution.
引用
收藏
页码:1623 / 1626
页数:4
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