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首页> 外文期刊>Angewandte Chemie >Regioselective Synthesis of γ-Amino Esters, Nitriles, Sulfones, and Pyrrolidinones by Nickel-Catalyzed Reductive Coupling of Aldimines and Activated Alkenes
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Regioselective Synthesis of γ-Amino Esters, Nitriles, Sulfones, and Pyrrolidinones by Nickel-Catalyzed Reductive Coupling of Aldimines and Activated Alkenes

机译:镍催化的醛亚胺和活化的烯烃的还原偶合反应选择性合成γ-氨基酯,腈,砜和吡咯烷酮

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摘要

The transition-metal-catalyzed regioselective coupling of two organic π components via a five-membered metallacycle intermediate is one method for the construction of C—C bonds and the synthesis of molecules with multiple functional groups. Among these reactions, the reductive coupling of alkyne/alkyne alkene/alkyne, and alkene/alkene couples has been widely explored by us and others. Similarly, the coupling of alkene/carbonyl and alkyne/carbonyl couples catalyzed by metal complexes has more recently also attracted attention.
机译:经由五元金属环中间体的过渡金属催化的两个有机π组分的区域选择性偶联是一种构建CC键和合成具有多个官能团的分子的方法。在这些反应中,炔烃/炔烃,烯烃/炔烃和烯烃/烯烃对的还原偶联已被我们和其他人广泛研究。类似地,最近由金属络合物催化的烯烃/羰基和炔烃/羰基的偶合也引起了关注。

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