Metal-Free Selective C-S Bond Cleavage of Thioethers to Access β-Alkoxy Carbonyl Compounds

被引:3
作者
Li, Yi [1 ]
Hu, Qingyue [1 ]
Zhang, Feiyang [1 ]
Li, Zhengyi [1 ]
Sun, Xiaoqiang [1 ]
Yang, Ke [1 ]
机构
[1] Changzhou Univ, Sch Petrochem Engn, Jiangsu Key Lab Adv Catalyt Mat & Technol, 1 Gehu Rd, Changzhou 213164, Jiangsu, Peoples R China
来源
CHEMISTRYSELECT | 2021年 / 6卷 / 24期
基金
中国国家自然科学基金;
关键词
C-S bond cleavage; C-O bond formation; Michael addition; Synthetic methods; Selectfluor; VERSATILE MEDIATOR; FLUORINATION; SELECTFLUOR; TRIFLUOROMETHYLATION; BORYLATION; ACTIVATION; CATALYST; SULFUR;
D O I
10.1002/slct.202101925
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A metal-free C(sp(3))-S bond cleavage of beta-alkylthio carbonyl compounds in the presence of Selectfluor is described. This novel strategy realizes the C-S bond cleavage and subsequent C-O bond formation, providing a facile and efficient method to construct different important beta-alkoxy carbonyl compounds with moderate to good yields and good functional groups tolerance. Moreover, our mechanistic studies also prove that two different mechanisms including the oxidant and thionium ion intermediate pathway may exist in this process.
引用
收藏
页码:6268 / 6271
页数:4
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