Regioselective Suzuki-Miyaura Cross-Coupling Reactions of 2,6-Dichloroquinoxaline

被引：10
作者：
Ali, Iftikhar [1 ]
Siyo, Baraa [1 ]
Al-Soud, Yaseen [1 ,2 ]
Villinger, Alexander [1 ]
Langer, Peter [1 ,3 ]
机构：
[1] Univ Rostock, Inst Chem, D-18059 Rostock, Germany
[2] Al Al Bayt Univ, Fac Sci, Dept Chem, Al Mafraq 25115, Jordan
[3] Univ Rostock eV, Leibniz Inst Katalyse, D-18059 Rostock, Germany
来源：
SYNTHESIS-STUTTGART | 2012年 / 44卷 / 11期
关键词：
catalysis; palladium; Suzuki reaction; quinoxalines; regioselectivity; QUINOXALINE DERIVATIVES; BIOLOGICAL EVALUATION; PART II; AGENTS; 2-HALOQUINOXALINES; ECHINOMYCIN; INHIBITORS; TRIOSTIN; BINDING;
D O I：
10.1055/s-0031-1289754
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
A variety of mono- and diarylated quinoxaline derivatives were prepared by site-selective Suzuki-Miyaura cross-coupling reactions of 2,6-dichloroquinoxaline. The selectivity is controlled by electronic parameters.
引用
收藏
页码：1637 / 1646
页数：10
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