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From Phenylhydrazone to 1<i>H</i>‐1,2,4‐Triazoles via Nitrification, Reduction and Cyclization

Liqiang Hao, Guodong Wang, Jian Sun, Jun Xu, Hongshuang Li, Guiyun Duan, Chengcai Xia, Pengfei Zhang

2020Advanced Synthesis & Catalysis35 citationsDOI

Abstract

Abstract Herein we report an annulation of phenylhydrazone via a tandem nitrification, reduction, cyclization protocol employing cobalt nitrate and 1,2‐dichloroethane to produce substituted 1 H ‐1,2,4‐triazoles. Notably, 1,2‐dichloroethane serves both the solvent and a hydrogen source for transfer hydrogenation. This methodology works under mild conditions, providing a direct approach for the synthesis of 1 H ‐1,2,4‐triazoles. magnified image

Topics & Concepts

ChemistryAnnulationTandemSolventCombinatorial chemistryReduction (mathematics)NitrificationDichloroethaneMedicinal chemistryOrganic chemistryCatalysisNitrogenGeometryMathematicsComposite materialMaterials scienceCatalytic C–H Functionalization MethodsSynthesis and Catalytic ReactionsAsymmetric Hydrogenation and Catalysis
From Phenylhydrazone to 1<i>H</i>‐1,2,4‐Triazoles via Nitrification, Reduction and Cyclization | Litcius