Site-selective Suzuki-Miyaura reactions of 2,6-dichlorobenzoxazole

被引:7
作者
Hamdy, Aws M. [1 ]
Eleya, Nadi [1 ]
Mohammed, Hamid H. [1 ,2 ]
Patonay, Tamas [3 ]
Spannenberg, Anke [4 ]
Langer, Peter [1 ,4 ]
机构
[1] Univ Rostock, Inst Chem, D-18059 Rostock, Germany
[2] Univ Al Mustansiriyah, Dept Organ Chem, Baghdad, Iraq
[3] Univ Debrecen, Dept Organ Chem, H-4032 Debrecen, Hungary
[4] Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany
关键词
Benzoxazole; Site-selectivity; Palladium; Catalysis; Suzuki-Miyaura reaction; CROSS-COUPLING REACTIONS; PARALLEL SYNTHESIS; BENZOXAZOLES; 2-ARYLBENZOXAZOLES; ARYLATION; CHLORIDES; BROMIDES; LIBRARY; BASES;
D O I
10.1016/j.tet.2012.11.021
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Suzuki-Miyaura reactions of 2,6-dichlorobenzoxazole provide a convenient access to arylated benzoxazoles. The reactions proceed with excellent site-selectivity in favour of position 2, due to electronic reasons. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2081 / 2086
页数:6
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