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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 >A novel approach to functionalized (E)-1,4-diaryl-l-butenes by Heck reaction and their applications for the construction of dibenzylbutyrolactone lignan skeletons by radical cyclization
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A novel approach to functionalized (E)-1,4-diaryl-l-butenes by Heck reaction and their applications for the construction of dibenzylbutyrolactone lignan skeletons by radical cyclization

机译:通过Heck反应官能化(E)-1,4-二芳基-1-丁烯的新方法及其在自由基环化反应中构建二苄基丁内酯木脂素骨架的应用

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摘要

A highly regio- and stereoselective [Pd(allyl)Cl]_2 catalyzed Heck reaction of aryl iodides and electronically neutral terminal olefins generated in situ by fluoride induced protiodesilylation of alkenylsilanol derivatives under mild conditions has been developed.The products,viz.terminally substituted styrenes and (E)-1,4-diaryl-l-butenes were obtained in very good yields.The dibenzylbutyrolactone lignan skeletons have been prepared employing two regio- and stereoselective Bu_3SnH-mediated radical cyclization routes.
机译:在温和的条件下,氟化物诱导的烯基硅烷醇衍生物的丙二硅烷基化反应可在原位生成芳基碘和电子中性末端烯烃的高度区域选择性和立体选择性[Pd(烯丙基)Cl] _2催化的Heck反应。已开发的产品是末端取代的苯乙烯(E)-1,4-二芳基-1-丁烯的收率非常高。采用两个区域和立体选择性Bu_3SnH介导的自由基环化途径制备了二苄基丁内酯木脂素骨架。

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