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首页> 外文期刊>European journal of inorganic chemistry >Activated aryl chlorides: Useful partners for the coupling with 2-substituted thiazoles in the palladium-catalysed C-H activation/functionalisation reaction
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Activated aryl chlorides: Useful partners for the coupling with 2-substituted thiazoles in the palladium-catalysed C-H activation/functionalisation reaction

机译:活化的芳基氯化物:在钯催化的C-H活化/官能化反应中与2-取代的噻唑偶联的有用伙伴

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摘要

Aryl chlorides are noticeably uncommon partners in coupling reactions with heteroaromatics through C-H activation. We report herein that as little as 1 mol-% of the air-stable PdCl(dppb)(C3H5) complex catalyses the direct coupling of electron-deficient aryl chlorides with 2-substituted thiazole derivatives. A range of functionalities on the aryl chloride such as acetyl, formyl, ester, nitro, nitrile or trifluoromethyl is tolerated. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)
机译:在通过C-H活化与杂芳族化合物偶联反应中,芳基氯化物显然是罕见的伴侣。我们在本文中报道,低至1 mol%的空气稳定的PdCl(dppb)(C3H5)络合物催化缺电子的芳基氯与2-取代的噻唑衍生物的直接偶联。在芳基氯上的一系列官能度是可接受的,例如乙酰基,甲酰基,酯,硝基,腈或三氟甲基。 ((C)Wiley-VCH Verlag GmbH&Co.KGaA,69451 Weinheim,Germany,2007)

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