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首页> 外文期刊>Advanced synthesis & catalysis >Substituent Effect in the Synthesis of alpha,alpha-Dibromoketones, 1,2-Dibromalkenes, and 1,2-Diketones from the Reaction of Alkynes and Dibromoisocyanuric Acid
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Substituent Effect in the Synthesis of alpha,alpha-Dibromoketones, 1,2-Dibromalkenes, and 1,2-Diketones from the Reaction of Alkynes and Dibromoisocyanuric Acid

机译:从炔烃和二溴氰脲酸反应中合成α,α-二溴氧基酮,1,2-二溴烷烃和1,2-二酮的取代基

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摘要

Internal alkynes reacted with dibromoisocyanuric acid/H2O to afford alpha,alpha-dibromoketone and 1,2-diketone derivatives. Diarylalkynes with activating groups provided 1,2-diketone derivatives as the major products, whereas diarylalkynes with a non-activating group or alkylarylalkynes gave alpha,alpha-dibromoketone derivatives as the major products. In addition, diarylalkynes with deactivating groups provided 1,2-dibromoalkenes. The reaction was conducted at room temperature and showed good yields in most cases. Reaction pathways have been proposed on the basis of experimental observations and density functional theory (DFT) calculations.
机译:内部炔烃与二溴异氰尿酸/ H2O反应,得到α,α-二溴氧基酮和1,2-二酮衍生物。 具有活性组的二芳基碱为主要产品提供1,2-Diketone衍生物,而具有非激活组或烷基芳基γ的二芳基胺将α-Dibromoketone衍生物作为主要产品。 另外,具有失活组的二芳基碱提供1,2-二溴烯烃。 在室温下进行反应,在大多数情况下表现出良好的产率。 已经基于实验观察和密度泛函(DFT)计算提出了反应途径。

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