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Reusable ionic liquid-catalyzed oxidative coupling of azoles and benzylic compounds via sp3 C–N bond formation under metal-free conditions†
Wenbo Liu,Chenjiang Liu,Yonghong Zhang,Yadong Sun,Ablimit Abdukadera,Bin Wang,He Li,Xuecheng Ma,Zengpeng Zhang
Organic & Biomolecular Chemistry Pub Date : 06/02/2015 00:00:00 , DOI:10.1039/C5OB00781J
Abstract

The heterocyclic ionic liquid-catalyzed direct oxidative amination of benzylic sp3 C–H bonds via intermolecular sp3 C–N bond formation for the synthesis of N-alkylated azoles under metal-free conditions is reported for the first time. The catalyst 1-butylpyridinium iodide can be recycled and reused with similar efficacies for at least eight cycles.

Graphical abstract: Reusable ionic liquid-catalyzed oxidative coupling of azoles and benzylic compounds via sp3 C–N bond formation under metal-free conditions
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