期刊论文详细信息
Journal of the Brazilian Chemical Society | |
Metal chloride hydrates as Lewis acid catalysts in multicomponent synthesis of 2,4,5-triarylimidazoles or 2,4,5-triaryloxazoles | |
Fontoura, Luiz A. M.1  Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil1  Universidade Luterana do Brasil, Canoas, Brazil1  Marques, Marcelo V.1  Ruthner, Marcelo M.1  Fundação de Ciência e Tecnologia, Cachoeirinha, Brazil1  Russowsky, Dennis1  | |
关键词: triarylimidazoles; triaryloxazoles; multicomponent reaction; metal halide hydrates; Lewis acids; Radziszewski reaction; benzil; benzoin; | |
DOI : 10.1590/S0103-50532012000100024 | |
学科分类:化学(综合) | |
来源: SciELO | |
【 摘 要 】
A series of nine metal chloride hydrates (ZnCl2.2H2O, SnCl2.2H2O, CdCl2.2H2O, MnCl2.4H2O, CoCl2.6H2O, SrCl2.6H2O, NiCl2.6H2O, CrCl3.6H2O and CeCl3.7H2O) was investigated as mild and inexpensive Lewis acid catalysts to promote the multicomponent synthesis of triarylimidazoles. Reactions starting from benzil showed the best results when SnCl2.2H2O was used, while for benzoin as the starting material, CeCl3.7H2O was more efficient. All reactions were performed in EtOH as solvent. These catalysts were also successfully employed in the synthesis of triaryloxazoles.
【 授权许可】
Unknown
【 预 览 】
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