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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
Author(s) -
Wang QingQing,
Jiang YangYe,
Zeng ChengChu,
Sun BaoGuo
Publication year - 2019
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.201800560
Subject(s) - chemistry , amine gas treating , electrochemistry , yield (engineering) , oxidative coupling of methane , phenols , coupling (piping) , oxidative phosphorylation , redox , photochemistry , combinatorial chemistry , organic chemistry , electrode , biochemistry , catalysis , mechanical engineering , materials science , engineering , metallurgy
Summary of main observation and conclusion An efficient electrochemical access to the non‐symmetric biphenols using tri( p ‐bromophenyl)amine (TBPA) as a redox mediator has been developed. The electrochemical protocol features highly selective cross‐coupling products in up to 83% yield, instead of forming homo‐coupling ones.
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