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首页> 外文期刊>Angewandte Chemie >Reductive C2-Alkylation of Pyridine and Quinoline N-Oxides Using Wittig Reagents
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Reductive C2-Alkylation of Pyridine and Quinoline N-Oxides Using Wittig Reagents

机译:使用Wittig试剂还原C2-烷基化吡啶和喹啉N-氧化物

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摘要

The ability to alkylate pyridines and quinolines is important for their further development as pharmaceuticals and agrochemicals, and for other purposes. Herein we describe the unprecedented reductive alkylation of pyridine and quinoline N-oxides using Wittig reagents. A wide range of pyridine and quinoline N-oxides were converted into C2-alkylated pyridines and quinolines with excellent site selectivity and functional-group compatibility. Sequential C-H functionalization reactions of pyridine and quinoline N-oxides highlight the utility of the developed method. Detailed labeling experiments were performed to elucidate the mechanism of this process.
机译:烷基化吡啶和喹啉的能力对于其作为药物和农用化学品的进一步发展是重要的,以及其他目的是重要的。 在此,我们描述了使用Wittig试剂的前所未有的吡啶和喹啉N-氧化物的还原烷基化。 将各种吡啶和喹啉N-氧化物转化为C2-烷基化吡啶和喹啉,具有优异的位点选择性和官能团相容性。 吡啶和喹啉N-氧化物的顺序C-H官能化反应突出了开发方法的效用。 进行详细的标记实验以阐明该方法的机制。

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