详细信息
A facile, catalyst- and additive-free, and scalable approach to the photochemical preparation of disulfides from organosulfenyl chlorides ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:A facile, catalyst- and additive-free, and scalable approach to the photochemical preparation of disulfides from organosulfenyl chlorides
作者:Liu, Wei[1,2];Wang, Jiayi[1];Song, Gonghua[1]
机构:[1]East China Univ Sci & Technol, Sch Pharm, Shanghai Key Lab Chem Biol, Shanghai 200237, Peoples R China;[2]State Key Lab Fluorine Containing Funct Membrane M, Zibo 256400, Shandong, Peoples R China
年份:2024
卷号:14
期号:44
起止页码:32200
外文期刊名:RSC ADVANCES
收录:;EI(收录号:20244217226867);WOS:【SCI-EXPANDED(收录号:WOS:001329964100001)】;
语种:英文
外文关键词:Free radical reactions - Reaction kinetics
摘要:A novel, clean and efficient protocol for the preparation of disulfides has been developed through the photochemical radical homo- and cross-coupling reaction of sulfenyl chlorides under LED irradiation and without the use of any catalyst and additive. The representative photochemical homo-coupling of trichloromethyl sulfenyl chloride has been successfully conducted on kilogram-scale in a continuous flow mode. The solvent and the main byproduct can be recovered in high yields, which makes the approach be highly atom economical. Various disulfides were prepared by the homo- and cross-coupling of sulfenyl chlorides under LED irradiation without the use of any catalyst or additive. The representative reaction was performed on kilogram-scale in a continuous flow mode.
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