首页> 外文期刊>Journal of Organometallic Chemistry >Nickel-catalyzed cross-coupling of organoaluminum reagents with alkynylhalides for the synthesis of symmetrical and unsymmetrical conjugated 1,3-diynes derivatives
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Nickel-catalyzed cross-coupling of organoaluminum reagents with alkynylhalides for the synthesis of symmetrical and unsymmetrical conjugated 1,3-diynes derivatives

机译:镍催化的有机铝试剂的交叉偶联用炔基卤化物用于合成对称和非对称的缀合的1,3-迪杨衍生物

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摘要

We describe a convenient method for the synthesis of symmetrical and unsymmetrical conjugated 1,3-diynes from cross-coupling reactions of organoaluminum with alkynylhalides: The cross-coupling reaction of organoaluminum (0.75 mmol) with alkynylhalides (0.5 mmol) mediated by Ni(acac)(2) (5 mol %)/DPPE(10 mol%) at room temperature in DME may produce symmetrical and unsymmetrical conjugated 1,3-diynes in moderate to good yields(up to 98%) derivatives. Their structures have been determined by HRMS and H-1(C-13)NMR data. On the basis of the experimental results, a possible catalytic cycle has been proposed. (C) 2019 Elsevier B.V. All rights reserved.
机译:我们描述了一种方便的方法,用于合成来自有机铝的对称和非对称缀合的1,3-脱酰胺与炔基卤化物的交叉偶联反应:有机铝(0.75mmol)与炔基卤化物(0.5mmol)的交叉偶联反应(0.5mmol)介导的Ni(ACAC 在DME的室温下(2)(5mol%)/ DPPE(10mol%)可以在中等至良好的产率(高达98%)衍生物中产生对称和不对称的缀合的1,3-迪敏。 它们的结构已由HRMS和H-1(C-13)NMR数据确定。 在实验结果的基础上,提出了一种可能的催化周期。 (c)2019 Elsevier B.v.保留所有权利。

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