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首页> 外文期刊>Organic letters >Synthesis of E-Alkyl Alkenes from Terminal Alkynes via Ni-Catalyzed Cross-Coupling of Alkyl Halides with B-Alkenyl-9-borabicyclo[3.3.1]nonanes
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Synthesis of E-Alkyl Alkenes from Terminal Alkynes via Ni-Catalyzed Cross-Coupling of Alkyl Halides with B-Alkenyl-9-borabicyclo[3.3.1]nonanes

机译:镍催化卤代烷基卤与B-烯基-9-硼环[3.3.1]壬烷的交叉偶联反应,由末端炔烃合成末端烷基烯烃

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摘要

The first Ni-catalyzed Suzuki-Miyaura coupling of alkyl halides with alkenyl-(9-BBN) reagents is reported. Both primary and secondary alkyl halides including alkyl chlorides can be coupled. The coupling method can be combined with hydroboration of terminal alkynes, allowing the expedited synthesis of functionalized alkyl alkenes from readily available alkynes with complete (E)-selectivity in one pot. The method was applied to the total synthesis of (+/-)-Recifeiolide, a natural macrolide.
机译:报道了烷基卤与烯基-(9-BBN)试剂的第一个Ni催化的Suzuki-Miyaura偶联反应。包括烷基氯的伯烷基卤和仲烷基卤都可以偶联。该偶联方法可以与末端炔烃的硼氢化反应结合使用,从而可以在一锅中从容易获得的炔烃中以完全(E)选择性加速合成官能化的烷基烯烃。该方法应用于天然大环内酯(+/-)-Recifeiolide的全合成。

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