Synthesis, microwave-promoted catalytic activity in Suzuki-Miyaura cross-coupling reactions and antimicrobial properties of novel benzimidazole salts bearing trimethylsilyl group

被引:40
作者
Yilmaz, Ulku [1 ]
Kucukbay, Hasan [1 ]
Sireci, Nihat [2 ]
Akkurt, Mehmet [3 ]
Gunal, Selami [4 ]
Durmaz, Riza [4 ]
Tahir, M. Nawaz [5 ]
机构
[1] Inonu Univ, Fac Sci & Arts, Dept Chem, TR-44280 Malatya, Turkey
[2] Adiyaman Univ, Fac Educ, TR-02040 Adiyaman, Turkey
[3] Erciyes Univ, Fac Sci, Dept Phys, TR-38039 Kayseri, Turkey
[4] Inonu Univ, Fac Med, Dept Microbiol, TR-44280 Malatya, Turkey
[5] Univ Sargodha, Dept Phys, Sargodha, Pakistan
关键词
benzimidazole salt; carbene; palladium catalysis; coupling reaction; Suzuki-Miyaura coupling; microwave; antimicrobial activity; CARBENE COMPLEXES; SUBSTITUTED BENZIMIDAZOLE; ARYL CHLORIDES; PALLADIUM; HECK; ANTIBACTERIAL; PRECATALYSTS; DERIVATIVES; SYSTEM; WATER;
D O I
10.1002/aoc.1772
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A mixture of benzimidazole salts (2-7), Pd(OAc)(2) and K2CO3 in DMF-H2O catalyzes the Suzuki-Miyaura cross-coupling reactions promoted by microwave irradiation resulting in high yield within a short time. In particular, the yield of the Suzuki-Miyaura reactions with aryl bromides was found to be nearly quantitative. The synthesized benzimidazole salts (2-7) were identified by H-1-C-13, NMR, IR spectroscopic methods and microanalysis. The molecular structure of 1 was determined by X-ray crystallography. The antibacterial and antifungal activities of the novel benzimidazole derivatives (1-7) were also tested against standard strains. Copyright (C) 2011 John Wiley & Sons, Ltd.
引用
收藏
页码:366 / 373
页数:8
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