Organic Solvent-Free, Pd(II)-Salan Complex-Catalyzed Synthesis of Biaryls via Suzuki-Miyaura Cross-Coupling in Water and Air

被引:31
作者
Bunda, Szilvia [1 ]
Udvardy, Antal [1 ]
Voronova, Krisztina [1 ,3 ]
Joo, Ferenc [1 ,2 ]
机构
[1] Univ Debrecen, Dept Phys Chem, POB 400, H-4002 Debrecen, Hungary
[2] Univ Debrecen, MTA DE Redox & Homogeneous Catalyt React Mech Res, POB 400, H-4002 Debrecen, Hungary
[3] Univ Nevada, Dept Chem, Reno, NV 89557 USA
关键词
AQUEOUS-PHASE; ARYLBORONIC ACIDS; ARYL CHLORIDES; SCHIFF-BASES; PALLADIUM; EFFICIENT; SONOGASHIRA; LIGANDS; HECK; CONVENIENT;
D O I
10.1021/acs.joc.8b02340
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
With use of a Pd(II)-sulfosalan complex as a water-soluble catalyst, we have developed an efficient synthesis of biaryls via Suzuki-Miyaura cross-coupling in water under aerobic conditions. The water-insoluble target molecules were isolated by simple filtration in analytical purity after washing with 0.01 M aqueous HCl (20 examples). In most cases, palladium contamination was below 5 ppm considered acceptable for active pharmaceutical ingredients. The established method is scalable, reproducible, and provides biaryl products in isolated yields up to 91%.
引用
收藏
页码:15486 / 15492
页数:7
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