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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 >Synthesis of arylsulfonyl-quinones and arylsulfonyl-1,4-diols as FabH inhibitors: Pd-catalyzed direct C-sulfone formation by C-S coupling of quinones with arylsulfonyl chloride
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Synthesis of arylsulfonyl-quinones and arylsulfonyl-1,4-diols as FabH inhibitors: Pd-catalyzed direct C-sulfone formation by C-S coupling of quinones with arylsulfonyl chloride

机译:FabH抑制剂的芳基磺酰基-醌和芳基磺酰基-1,4-二醇的合成:醌与芳基磺酰氯的C-S偶联,钯催化直接C-砜的形成

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摘要

The Pd-catalyzed direct C-sulfone formation by C-S coupling of quinones with arylsulfonyl chloride has been developed. This methodology provides an effective, convenient method for the synthesis of arylsulfonyl-quinones and arylsulfonyl-1,4-diols, which are potent inhibitors of FabH.
机译:已经开发了通过醌与芳基磺酰氯的C-S偶联来Pd催化的直接C-砜形成。该方法提供了一种有效,方便的方法,用于合成芳基磺酰基-醌和芳基磺酰基-1,4-二醇,它们是FabH的有效抑制剂。

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