Copper-Catalyzed Three-Component Reaction of Oxadiazoles, Elemental Se/S and Aryl Iodides: Synthesis of Chalcogenyl (Se/S)-Oxadiazoles

被引:31
作者
Peterle, Marcos M. [1 ]
Scheide, Marcos R. [1 ]
Silva, Lais T. [1 ]
Saba, Sumbal [1 ]
Rafique, Jamal [1 ,2 ]
Braga, Antonio L. [1 ]
机构
[1] Univ Fed Santa Catarina, Dept Quim, Labselen, BR-88040900 Florianopolis, SC, Brazil
[2] Univ Fed Mato Grosso do Sul, Inst Quim, BR-79074460 Campo Grande, MS, Brazil
来源
CHEMISTRYSELECT | 2018年 / 3卷 / 46期
基金
巴西圣保罗研究基金会;
关键词
C(sp(2))-H bond chalcogenation; CuI; oxadiazole; selenide; sulfide; HETEROATOM BOND FORMATION; BIOLOGICAL EVALUATION; EFFICIENT SYNTHESIS; 1,3,4-OXADIAZOLES; FUNCTIONALIZATION; NANOPARTICLES; CYCLOADDITION; SELENYLATION; THIOLATION; OXIDATION;
D O I
10.1002/slct.201801213
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An efficient copper-catalyzed three-component chalcogenation of oxadiazoles with elemental selenium/sulfur and aryl iodide is described herein. This one-pot C(sp(2))-H bond chalcogenation approach is attractive and practical, since a cheap copper catalyst is employed with minimum catalytic loading, in an open-to-air atmosphere. Under optimized conditions, that reaction provides a wide range of structurally diverse organochalcogenyl (Se/S)-oxadiazoles in good to excellent yields with good functional group tolerance. This practical approach represents a valuable contribution to synthetic and medicinal chemistry, providing an important addition to the current C-Se/S bond formation chemistry scenario.
引用
收藏
页码:13191 / 13196
页数:6
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