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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Nickel-catalyzed cross-coupling reaction of acetylenic sulfones with alkynyl Grignard reagents: a facile method for the preparation of unsymmetrical 1,3-diynes
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Nickel-catalyzed cross-coupling reaction of acetylenic sulfones with alkynyl Grignard reagents: a facile method for the preparation of unsymmetrical 1,3-diynes

机译:乙炔砜与炔基格氏试剂的镍催化交叉偶联反应:制备不对称1,3-二炔的简便方法

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摘要

The cross-coupling reaction of acetylenic sulfones with acetylenic Grignard reagents was realized by using Ni(acac)2 as catalyst to afford unsymmetrical 1,3-diynes under mild conditions without homocou-pling byproducts. By using this method, 1,4-diaryl-1,3-diynes could be obtained in moderate to good yields (59-83%), whereas, the yields for alkyl substituted 1,3-diynes are lower (30-54%).
机译:乙炔砜与乙炔格氏试剂的交叉偶联反应是通过使用Ni(acac)2作为催化剂在温和条件下提供不对称1,3-二炔而没有均聚副产物而实现的。通过使用这种方法,可以中等至良好的产率(59-83%)获得1,4-二芳基-1,3-二炔,而烷基取代的1,3-二炔的产率较低(30-54%)。 )。

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