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首页> 外文期刊>Angewandte Chemie >Modular Synthesis of alpha-Quaternary Chiral beta-Lactams by a Synergistic Copper/Palladium-Catalyzed Multicomponent Reaction
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Modular Synthesis of alpha-Quaternary Chiral beta-Lactams by a Synergistic Copper/Palladium-Catalyzed Multicomponent Reaction

机译:通过协同铜/钯催化的多组分反应进行α-季肾上腺β-内酰胺的模块化合成

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摘要

An asymmetric multicomponent, interrupted Kinugasa allylic alkylation (IKAA) reaction has been developed with a synergistic Cu-catalyzed Kinugasa system and a Pd-catalyzed allylic alkylation reaction. This unprecedented reaction provides in high yields and with high stereoselectivity a synthesis of alpha-quaternary chiral beta-lactams, which cannot be produced with existing synthetic methods. Stereoselective coupling of two catalytic amounts of transient organometallic intermediates formed in situ is an important feature of this reaction.
机译:利用铜催化的Kinugasa体系和钯催化的烯丙基烷基化反应,发展了一种不对称多组分间断Kinugasa烯丙基烷基化反应(IKAA)。这一前所未有的反应以高收率和高立体选择性合成了现有合成方法无法生产的α-四元手性β-内酰胺。这种反应的一个重要特点是,两种催化量的原位形成的过渡金属有机中间体的立体选择性偶联。

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