首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Unexpected S_N2'-type addition-elimination reactions of 1-aryl-2,3-allenols with LiX. Synthesis and synthetic application of 1-aryl-3-halo-1,3-dienes
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Unexpected S_N2'-type addition-elimination reactions of 1-aryl-2,3-allenols with LiX. Synthesis and synthetic application of 1-aryl-3-halo-1,3-dienes

机译:1-芳基-2,3-烯醇与LiX的意外S_N2'型加成消除反应。 1-芳基-3-卤代-1,3-二烯的合成及合成应用

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摘要

1-Aryl-3-halo-1,3-dienes were prepared from the sequential addition - elimination reaction of 1-aryl-2,3-allenols with LiX (X = Br, Cl) in HOAc in moderate to good yields. Here the aromatic substituent is crucial to this interesting transformation since no reaction was observed with 1-alkyl or perfluoroalkyl-2,3-allenols. The 1-aryl-3-halo-1,3-dienes prepared can be used as useful partners in Diels-Alder reactions with dienophiles leading to polycyclic quinone derivatives.
机译:1-芳基-3-卤代-1,3-二烯是由1-芳基-2,3-烯醇与LiX(X = Br,Cl)在HOAc中的顺序加成-消除反应制得的,产率中等至良好。在这里,芳族取代基对于这种有趣的转化至关重要,因为未观察到与1-烷基或全氟烷基-2,3-烯醇的反应。制备的1-芳基-3-卤代-1,3-二烯可用作与亲二烯体形成多环醌衍生物的狄尔斯-阿尔德反应的有用伴侣。

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