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首页> 外文期刊>Indian Journal of Chemistry, Section B. Organic Including Medicinal >Facile formation of bis(3-indolyl)methyl- arenes by iodine-catalyzed reaction of indole with alpha,alpha'-bis(arylmethylene)ketones and alpha-substituted arylmethyleneketones in dry ethanol
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Facile formation of bis(3-indolyl)methyl- arenes by iodine-catalyzed reaction of indole with alpha,alpha'-bis(arylmethylene)ketones and alpha-substituted arylmethyleneketones in dry ethanol

机译:在无水乙醇中通过碘催化吲哚与α,α'-双(芳基亚甲基)酮和α-取代的芳基亚甲基酮的反应,轻松形成双(3-吲哚基)甲基-芳烃

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摘要

Bis(3-indolyl)methylarenes are obtained in good yield by reaction of indole with alpha,alpha'-bis(arylmethylene)ketones and alpha-substituted arylmethyleneketones in dry ethanol using catalytic amount of molecular iodine at room temperature.A plausible mechanism for formation of these products has been suggested.
机译:通过在室温下使用催化量的分子碘将吲哚与α,α'-双(芳基亚甲基)酮和α-取代的芳基亚甲基酮反应在干乙醇中以高收率获得双(3-吲哚基)甲基芳烃。建议使用这些产品。

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