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首页> 外文期刊>Angewandte Chemie >Tetraarylphosphonium Halides as Arylating Reagents in Pd-Catalyzed Heck and Cross-Coupling Reactions
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Tetraarylphosphonium Halides as Arylating Reagents in Pd-Catalyzed Heck and Cross-Coupling Reactions

机译:四芳基Hal卤化物在Pd催化的Heck和交叉偶联反应中作为丙烯酸化试剂

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摘要

Transition-metal-catalyzed olefination and cross-coupling reactions have become one of the most powerful tools in organic synthesis.While aryl,alkenyl,alkynyl,and,more recently,alkyl halides are typically employed as coupling reagents,a variety of different types of pseudohalide species have been also investigated as useful electrophiles.Among these,representative recent examples are carboxylic acids,acid anhydrides,aryl esters,sulfonates,151 phosphonic acids,sulfonium ions,and ammonium salts.Although metal-mediated C-P bond cleavage of organophosphorus species was previously investigated,the use of such compounds in cross-coupling reactions has been relatively underdeveloped.
机译:过渡金属催化的烯化和交叉偶联反应已成为有机合成中最强大的工具之一。虽然芳基,烯基,炔基以及最近的烷基卤化物通常用作偶联剂,但各种不同类型的还研究了假卤化物作为有用的亲电子试剂。在这些实例中,代表性的例子是羧酸,酸酐,芳基酯,磺酸盐,151膦酸,ulf离子和铵盐。先前已经研究过,在交叉偶联反应中使用这类化合物还相对欠发达。

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