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Experimental and Theoretical Studies on Regiodivergent C-HAlkylation of Quinolines with Alkenes by Half-Sandwich Rare-EarthCatalysts

机译:半三明治稀土催化剂与喹啉喹啉喹啉羟烷基的实验与理论研究

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摘要

Quinoline is an important structural motif in pharmaceuticals,agrochemicals,and naturalproducts.The development of selective and efficient protocols for the synthesis of quinolinecontainingcompounds is therefore of great interest and importance.Among possibleapproaches,catalytic C-H addition to alkenes is the most atom-efficient route for the synthesisof alkylated quinoline derivatives.However,major efforts have been donated to the C-H bondalkylation of quinolines on the more reactive N-heterocyclic ring,while a selective C-Halkylation of quinolines on the carbocyclic ring remains largely underdeveloped.1
机译:喹啉是药物,农业化学品和天然产物的重要结构主题。因此,用于合成喹诺尼替尼划分的选择性和有效的协议是极大的兴趣和重要的。己二酸催化Ch的催化Ch是最有效的烷基化喹啉衍生物的合成。然而,在更反应性的正杂环上载入喹啉的CH键烷基化的主要努力,同时碳环环上的喹啉的选择性C-甲基化合物仍未欠发达。

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