详细信息

Highly Regioselective Synthesis of N-β-trifluoromethyl 2-pyridones via anti-Markovnikov Hydroamination of α-(trifluoromethyl)styrenes with 2-pyridones  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Highly Regioselective Synthesis of N-β-trifluoromethyl 2-pyridones via anti-Markovnikov Hydroamination of α-(trifluoromethyl)styrenes with 2-pyridones

作者:Zhang, Yi[1];Sun, Zhudi[1];He, Jingjing[1];Deng, Yupian[1];Liu, Ying[1];Zheng, Pai[1];Cao, Song[1,2]

机构:[1]East China Univ Sci & Technol ECUST, Shanghai Key Lab Chem Biol, Sch Pharm, Shanghai 200237, Peoples R China;[2]Chinese Acad Sci, Shanghai Inst Organ Chem, Key Lab Organofluorine Chem, Shanghai 200032, Peoples R China

年份:2023

卷号:18

期号:10

外文期刊名:CHEMISTRY-AN ASIAN JOURNAL

收录:;EI(收录号:20231713949521);WOS:【SCI-EXPANDED(收录号:WOS:000976298400001)】;

语种:英文

外文关键词:alpha-(trifluoromethyl)styrenes; hydroamination; N-beta-trifluoromethyl 2-pyridones; regioselectivity; 2-pyridones

摘要:A novel and facile method for the synthesis of N-beta-CF3-substituted 2-pyridones via hydroamination of alpha-(trifluoromethyl)styrenes with 2-pyridones was described. The reaction proceeded smoothly at room temperature, affording a variety of N-(beta-trifluoromethyl-beta-arylethyl)pyridin-2(1H)-ones in moderate to good yields with excellent N-regioselectivity.

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