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作 者:Fei Lian Feixian Luo Meng Wang Kun Xu Chengchu Zeng
机构地区:[1]Faculty of Environment and Life,Beijing University of Technology,Beijing,100124 China [2]Key Laboratory of Ecology and Environment in Minority Areas(Minzu University of China),National Ethnic Affairs Commission,Beijing,100081 China
出 处:《Chinese Journal of Chemistry》2023年第13期1583-1588,共6页中国化学(英文版)
基 金:the National Natural Science Foundation of China(21871019,21901263,22171015);Beijing Municipal Education Committee Project(KZ202110005003,KM202110005006);Beijing Natural Science Foundation(2222003).
摘 要:A new electrochemical strategy for the atom transfer radical addition(ATRA)of polychloroalkanes across olefins has been realized by the synergism of paired electrolysis and halogen bonding activation.Notably,readily accessible 4,4-di-tert-butyl bipyridine(dtbpy),acting as a halogen bonding acceptor,shifted the reduction potential of C—Cl bonds positively by 110 mV.The decreased operating potential leads to a wide substrate scope and excellent functional group compatibility.A diverse array of terminal and internal alkenes such as(hetero)aryl olefins,unactive aliphatic olefins,and natural products and drugs-derived olefins were well compatible.
关 键 词:ELECTROCATALYSIS Organohalides Atom transfer radical addition Radical-polar crossover ALKENES
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