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首页> 外文期刊>Synlett >Synthesis of alpha,beta-Unsaturated Ketones by Rhodium-Catalyzed Carbonylative Arylation of Internal Alkynes with Arylboronic Acids
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Synthesis of alpha,beta-Unsaturated Ketones by Rhodium-Catalyzed Carbonylative Arylation of Internal Alkynes with Arylboronic Acids

机译:铑催化内炔烃与芳基硼酸的羰基化羰基化合成α,β-不饱和酮

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摘要

The Rh-catalyzed reaction of arylboronic acids with internal alkynes under a CO atmosphere in the presence of an acid additive afforded alpha,beta-unsaturated ketones as the major products. Hydroacylation of internal alkynes, except in the case of diaryl acetylenes, proceeded in syn fashion, yielding the E-configured isomer. A mixture of E- and Z-isomers was obtained with diphenyl acetylene. Reactions were also highly regioselective for various nonsymmetric alkynes.
机译:在酸性添加剂存在下,在CO气氛下,芳基硼酸与内部炔烃进行Rh催化反应,得到α,β-不饱和酮为主要产物。除在二芳基乙炔的情况外,内部炔烃的加氢酰化以合成方式进行,得到E-构型的异构体。用二苯基乙炔得到E-和Z-异构体的混合物。对于各种非对称炔烃,反应也是高度区域选择性的。

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