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Recent Advances in Benzimidazole Based NHC-Metal Complex Catalysed Cross-Coupling Reactions

机译:基于苯依咪唑唑的最新进展

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In recent years,there has been a substantial increase in the development of efficient,environmentally compatible and cost-effective catalysts as a replacement for conventional metal catalysts.Among several catalysts developed,metal-based NHeterocyclic carbene(NHC)catalysts have garnered significant attention due to the unique steric and electronic properties imparted by NHCs,making them suitable for a broad spectrum of chemical transformations.Over a decade,benzimidazole based NHCs have been broadly investigated for the synthesis of metal complexes for a variety of catalytic processes.The interesting properties of benzimidazole scaffolds such as the ease of tailoring its electronic and steric properties via simple synthetic modifications,aids in achieving potential catalysts for cross-coupling reactions and other hydrofunctional transformations.This review focuses on the synthetic approaches developed over recent years(2015-2021)concerning the structural tuning and modulation of the benzimidazole derived NHC ligands to generate catalytically active metal complexes for cross-coupling reactions such as Heck,Suzuki,Sonogashira,Kumada and dehydrogenative cross-coupling reactions.
机译:近年来,有效,环境兼容且具有成本效益的催化剂的发展已大幅增长,以替代传统的金属催化剂。在开发的几种催化剂,基于金属的NHETEROCYCLIC Carbene(NHC)的催化剂中,催化剂已引起了重大关注。对于NHC所赋予的独特空间和电子特性,使其适合于广泛的化学转化。在十年中,基于苯甲酰唑的NHC已广泛研究了金属复合物的合成,用于多种催化过程。苯并咪唑支架,例如通过简单的合成修饰来轻松调整其电子和空间特性,有助于实现交叉偶联反应的潜在催化剂和其他水力函数转换。这本综述着重于近年来(2015-2021)的合成方法, BE的结构调整和调制Nzimidazole衍生出NHC配体生成催化活性的金属复合物,以进行交叉偶联反应,例如Heck,Suzuki,Sonogashira,Kumada和脱氢交叉偶联反应。

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