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硝酸银作为铑(III)催化偶氮苯合成2-芳基-2H-苯并三唑的氮源。

AgNO3 as nitrogen source for rhodium(iii)-catalyzed synthesis of 2-aryl-2H-benzotriazoles from azobenzenes.

作者信息

Li Jixing, Zhou Hui, Zhang Jinlong, Yang Huameng, Jiang Gaoxi

机构信息

State Key Laboratory for Oxo Synthesis and Selective Oxidation, Suzhou Research Institute of LICP, Lanzhou Institute of Chemical Physics (LICP), Chinese Academy of Sciences, Lanzhou 730000, P. R. China.

出版信息

Chem Commun (Camb). 2016 Jul 21;52(61):9589-92. doi: 10.1039/c6cc04341k.

Abstract

A new approach has been established for Rh(iii)-catalyzed direct aza oxidative cyclization of non-prefunctionalized azobenzenes to provide 2-aryl-2H-benzotriazoles in good yields, in which AgNO3 instead of conventional azide reagents for the first time functions as the nitrogen source for the nitrogenation reaction. Preliminary mechanistic studies suggest that the Rh(iii)-catalyst could account for the nitration reaction, and subsequently cationic silver species might both play a vital role in the fission of the nitrogen-oxygen bonds in nitro groups and promote aza oxidative cyclization.

摘要

已建立了一种新方法,用于铑(III)催化未预官能化偶氮苯的直接氮杂氧化环化反应,以良好的产率提供2-芳基-2H-苯并三唑,其中AgNO3首次替代传统的叠氮化物试剂作为氮杂反应的氮源。初步机理研究表明,铑(III)催化剂可引发硝化反应,随后阳离子银物种可能在硝基中氮-氧键的断裂中起关键作用,并促进氮杂氧化环化反应。

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