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作 者:Qiao Li Minjie Liu Meifen Jiang Li Wan Yingtang Ning Fen-Er Chen
机构地区:[1]College of Chemical Engineering,Zhejiang University of Technology,Hangzhou 310014,China [2]Engineering Center of Catalysis and Synthesis for Chiral Molecules,Fudan University,Shanghai 200433,China [3]Shanghai Engineering Center of Industrial Catalysis for Chiral Drugs,Shanghai 200433,China [4]Institute of Pharmaceutical Science and Technology,Zhejiang University of Technology,Hangzhou 310014,China
出 处:《Chinese Chemical Letters》2024年第2期366-369,共4页中国化学快报(英文版)
基 金:Financial support from the National Natural Science Foundation of China(No.22077018)is gratefully acknowledged.
摘 要:We report the photo-mediated 1,2-aryl migration of 2‑chloro-1-arylpropanones to 2-arylpropionic acids using HCOONa as an acid scavenger.This pragmatically focused study obviates the multiple-step sequence in the industrially employed,ZnO-promoted rearrangement strategy,and offers rapid access to various 2-arylpropionic acids under environmentally friendly conditions.Furthermore,the successful transfer of this batch photochemistry to a continuous flow platform led to improved scalability and enabled the gram-scale synthesis of loxoprofen.
关 键 词:Green chemistry Flow chemistry 2-Arylpropionic acids Photo-Favorskii reaction
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