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作 者:Li Liu Jing Wang Xiaoying Feng Kun Xu Wei Liu Xia Peng Hongguang Du Jiajing Tan
机构地区:[1]Department of Organic Chemistry,College of Chemistry,Beijing University of Chemical Technology,Beijing,100029 China [2]Sinopec Beijing Research Institute of Chemical Industry,Beijing,100013 China [3]Faculty of Environment and Life,Beijing University of Technology,Beijing,100124 China
出 处:《Chinese Journal of Chemistry》2024年第11期1230-1236,共7页中国化学(英文版)
基 金:support from the National Natural Science Foundation of China(21702013 and 22271010);the Fundamental Research Funds for the Central Universities(XK1802-6)at the BUCT.
摘 要:A visible-light-enabled,photocatalyst-free hydroacylation reaction of azodicarboxylic acid derivatives was described.This radical conjugate addition(RCA)protocol relied on the dual role of 4-acyl-1,4-dihydropyridine(acyl-DHP)reagents that besides being as radical reservoirs,they also enabled the conversion of radical adducts to anion intermediates via reduction.Under“catalyst-oxidant-additive free”conditions,a wide range of structurally different acyl hydrazide products were readily obtained in 56%—99%yields.The utility of this transformation was further demonstrated by the scale-up synthesis and downstream derivatization.
关 键 词:Azo compounds Radicals ACYLATION 4-Acyl-1 4-dihydropyridine PHOTOCHEMISTRY
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