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首页> 外文期刊>Angewandte Chemie >Decarboxylative Cross-Coupling of Mesylates Catalyzed by Copper/ Palladium Systems with Customized Imidazolyl Phosphine Ligands
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Decarboxylative Cross-Coupling of Mesylates Catalyzed by Copper/ Palladium Systems with Customized Imidazolyl Phosphine Ligands

机译:铜/钯体系与定制的咪唑基膦配体催化的甲磺酸酯的脱羧交叉偶联

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摘要

Decarboxylative cross-coupling reactions have recently emerged as a powerful methodology for the regioselective construction of C—C and C—heteroatom bonds. Their key advantage over traditional cross-coupling reactions is that they draw on stable and readily available carboxylate salts as sources of carbon nucleophiles rather than expensive and sensitive organometallic reagents. In the last decade, a rapidly growing number of decarboxylative reactions have been discovered including decarboxylative Heck reactions, ally-lations, redox-neutral cross-coupling reactions, oxidative coupling reactions, C—H arylations, homocouplings, and Chan-Lam-type reactions.
机译:脱羧交叉偶联反应最近已成为一种强有力的方法,用于进行C和C和C-杂原子键的区域选择性构建。与传统的交叉偶联反应相比,它们的关键优势在于它们利用稳定且易于获得的羧酸盐作为碳亲核试剂的来源,而不是昂贵且敏感的有机金属试剂。在过去的十年中,发现了数量迅速增长的脱羧反应,包括脱羧Heck反应,烯丙基化,氧化还原-中性交叉偶联反应,氧化偶联反应,CH芳基化,均偶联和Chan-Lam型反应。

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