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首页> 外文期刊>Angewandte Chemie >Acid-Catalyzed Direct Conjugate Alkenylation of α,β-Unsaturated Ketones
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Acid-Catalyzed Direct Conjugate Alkenylation of α,β-Unsaturated Ketones

机译:酸催化的α,β-不饱和酮的直接共轭烯化

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摘要

The conjugate addition reaction to α,β-unsaturated carbonyl compounds is one of the most fundamental reactions in organic chemistry. It is a powerful and reliable tool for the formation of carbon-carbon bonds. Numerous C—C bond-forming conjugate addition reactions involve the nucleophilic attack of a carbanion species (known as Michael-type reactions), thus generally affording stoichiometric amounts of metal salts as waste products. Nowadays, from an environmental point of view, the reduction of waste in organic reactions is one of the most important issues to solve. For alkenylation reactions, alkenylmetal reagents are often used in the conjugate alkenylation of enones (Scheme la).
机译:α,β-不饱和羰基化合物的共轭加成反应是有机化学中最基本的反应之一。它是形成碳-碳键的强大而可靠的工具。许多形成CC键的共轭加成反应涉及碳负离子物种的亲核攻击(称为迈克尔型反应),因此通常提供化学计量的金属盐作为废品。如今,从环境角度看,减少有机反应中的废物是最重要的问题之一。对于烯基化反应,烯基金属试剂经常用于烯酮的共轭烯基化(方案1a)。

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