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首页> 外文期刊>Angewandte Chemie >Organosulfur Compounds:Electrophilic Reagents in Transition-Metal-Catalyzed Carbon-Carbon Bond-Forming Reactions
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Organosulfur Compounds:Electrophilic Reagents in Transition-Metal-Catalyzed Carbon-Carbon Bond-Forming Reactions

机译:有机硫磺化合物:在过渡金属催化的碳 - 碳键 - 形成反应中的亲电子试剂

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摘要

Transition-metal-catalyzed carbon-carbon bond-forming reactions are among the most powerful methods in organic synthesis and play a crucial role in modern materials science and medicinal chemistry.Recent developments in the area of ligands and additives permit the cross-coupling of a large variety of reactants,including inexpensive and readily available sulfonyl chlorides.Their desulfitative carbon-carbon cross-coupling reactions (Negishi,Stille,carbonylative Stille,Suzuki-Miyaura,and Sonogashira-Hagihara-type cross-couplings and Mizoroki-Heck-type arylations) are reviewed together with carbon-carbon cross-coupling reactions with other organosulfur compounds as electrophilic reagents.
机译:过渡金属催化的碳 - 碳键形成反应是有机合成中最强大的方法,在现代材料科学和药用化学中发挥至关重要的作用。配体和添加剂面积的经济发展允许交叉耦合 各种反应物,包括廉价且容易获得的磺酰氯。脱硫碳 - 碳交叉偶联反应(Negishi,Stille,羰基化stille,Suzuki-miyaura和Sonogashira-hagihara型交叉联轴器和Mizoroki-Heck型芳族 )与碳 - 碳交联反应与其他有机硫磺化合物一起进行审查,作为电泳试剂。

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