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Electrocatalytic Synthesis of Non-Symmetric Biphenols Mediated by Tri(p-bromophenyl)amine:Selective Oxidative Cross-Coupling of Different Phenols and Naphthols

NonSymmetric Biphenols 的 Electrocatalytic 合成由 Tri (pbromophenyl ) 胺调停了: 不同的酚和萘粉 <sup></sup> 的选择氧化 CrossCoupling

作     者:Qing-Qing Wang Yang-Ye Jiang Cheng-Chu Zeng Bao-Guo Sun 

作者机构:Beijing Advanced Innovation Center for Food Nutrition and Human HealthSchool of Food and Chemical EngineeringBeijing Technology and Business UniversityBeijing 100048China Beijing Key Laboratory of Environmental and Viral OncologyCollege of Life Science & BioengineeringBeijing University of TechnologyBeijing 100124China 

出 版 物:《Chinese Journal of Chemistry》 (中国化学(英文版))

年 卷 期:2019年第37卷第4期

页      面:352-358页

核心收录:

学科分类:07[理学] 0703[理学-化学] 

基  金:grants from the National Key Technology R&D Program(No.2016YFD0400801) the National Natural Science Foundation of China(No.21871019) 

主  题:Non-Symmetric Biphenols Mediated Tri(p-bromophenyl)amine Phenols Naphthols 

摘      要:An efficient electrochemical access to the non-symmetric biphenols using tri(p-bromophenyl)amine(TBPA)as a redox mediator has been *** electrochemical protocol features highly selective cross-coupling products in up to 83% yield,instead of forming homo-coupling ones.

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