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Gold-catalyzed approach to multisubstituted fulvenes via cycloisomerization of furan/ynes

机译:呋喃/炔的环异构化金催化多取代富烯的方法

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摘要

A new approach to functionalized fulvenes with an enone or enal moiety has been developed through gold-catalyzed intramolecular cycloisomerization of furan/ynes with a two-carbon tether in between the furan and the triple bond. The reaction proceeds with complete regioselectivity via a 6-endo-cyclization and high stereoselectivity. Moreover, the E- or Z-stereochemistry of the double bond in fulvene products can be easily controlled by performing the reaction in different solvents.
机译:通过金催化的呋喃/炔烃分子内呋喃和三键之间的二碳系链,开发了一种新的功能化烯酮或烯醛部分富烯的方法。通过6-内-环化和高立体选择性,反应以完全的区域选择性进行。而且,通过在不同溶剂中进行反应,可以容易地控制富烯产物中双键的E-或Z-立体化学。

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