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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 >Highly efficient synthesis of 2,3,4-trisubstituted furans via silver-catalyzed sequential nucleophilic addition and cyclization reactions of haloalkynes
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Highly efficient synthesis of 2,3,4-trisubstituted furans via silver-catalyzed sequential nucleophilic addition and cyclization reactions of haloalkynes

机译:通过银催化的卤代炔的连续亲核加成和环化反应高效合成2,3,4-三取代的呋喃

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摘要

A regioselective synthesis of 2,3,4-trisubstituted furans using AgNO3 catalyst from haloalkynes in a one-pot procedure has been reported. The transformation consists of a sequential silver-catalyzed nucleophilic addition and cyclization reaction of haloalkynes. A wide variety of haloalkynes can be used in this chemical process.
机译:已经报道了使用AgNO 3催化剂从卤代炔烃以一锅法进行区域选择性合成2,3,4-三取代的呋喃。该转化由卤代炔烃的连续银催化亲核加成和环化反应组成。在该化学过程中可以使用多种卤代炔烃。

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