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Library-friendly synthesis of fluorinated ketones through functionalized hydration of alkynes and investigation of the reaction mechanism

机译:通过炔烃的官能化水合,图书馆友好地合成氟化酮,并研究其反应机理

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摘要

A library-friendly synthesis of α-substituted-α-fluoroketones through functionalized hydration of alkynes in one pot under mild conditions is reported. The ready availability of alkynes and organoboronic acids makes this reaction quite attractive. We also studied the key intermediate—a fluorinated cationic gold species—using in situ NMR spectroscopy and ESI-high resolution mass spectrometry.
机译:据报道,在温和的条件下,通过在一个罐中炔烃的官能化水合,可以库化合成α-取代的α-氟代酮。炔烃和有机硼酸的现成可用性使该反应颇具吸引力。我们还使用原位NMR光谱和ESI高分辨率质谱研究了关键中间体-氟化阳离子金。

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