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首页> 外文期刊>Angewandte Chemie >Palladium-Catalyzed C—C Bond Formation To Construct 1,4-Diketones under Mild Conditions
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Palladium-Catalyzed C—C Bond Formation To Construct 1,4-Diketones under Mild Conditions

机译:钯催化CC键形成在温和条件下构建1,4-二酮

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摘要

Carbon-carbon bond formation is the central transformation in synthetic organic chemistry. Although there are a number of strategies to construct C—C bonds, nucleophilic substitution is perhaps the oldest and most widely used of these methods. These transformations typically involve primary alkyl halides or tosylates as electrophiles to couple with a variety of different nucleophiles. Direct substitution of a leaving group at a C(sp~2) center is not possible, while substitution is well known for secondary alkyl (C(sp~3)) positions even though this can still prove problematic.
机译:碳-碳键的形成是合成有机化学的主要转变。尽管有许多构建C-C键的策略,亲核取代也许是这些方法中最早,应用最广泛的方法。这些转化通常涉及伯烷基卤化物或甲苯磺酸盐作为亲电子试剂,以与多种不同的亲核试剂偶联。在C(sp〜2)中心不能直接取代一个离去基团,尽管对于仲烷基(C(sp〜3))位置而言,取代是众所周知的,尽管这仍然会造成问题。

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