Defluorinative Thiolation of gem-Difluoroalkenes by Convergent Paired Electrolysis

被引:10
|
作者
Pan, Zichen [1 ]
Wang, Xiuqi [1 ]
Zhao, Shuaishuai [2 ]
Deng, Hongping [3 ,4 ]
Ma, Mengtao [1 ]
Xue, Fei [1 ]
机构
[1] Nanjing Forestry Univ, Inst Mat Phys & Chem, Coll Sci, Nanjing 210037, Jiangsu, Peoples R China
[2] Nanjing Tech Univ, Inst Adv Synth, Sch Chem & Mol Engn, Nanjing 211816, Jiangsu, Peoples R China
[3] Nanjing Agr Univ, Jiangsu Key Lab Pesticide Sci, Nanjing 210095, Jiangsu, Peoples R China
[4] Nanjing Agr Univ, Coll Sci, Dept Chem, Nanjing 210095, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
CROSS-COUPLING REACTION; C-H; MONOFLUOROALKENES; ELECTROCHEMISTRY; FLUORINE; SULFIDES;
D O I
10.1021/acs.orglett.3c02235
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Herein, we have successfully developed a convergent pairedelectrolysisstrategy for the defluorinative thiolation process utilizing thiolsand gem-difluoroalkenes as precursors. This protocolexhibits remarkable tolerance toward a wide range of functional groups,as exemplified by the successful late-stage defluorothiolation ofcomplex molecules. Additionally, this strategy is amenable to gram-scalesynthesis, making use of both anodic oxidation and cathodic reductionprocesses in an efficient manner. Several control studies were conductedand suggested a convergent paired electrolysis mechanism.
引用
收藏
页码:6143 / 6148
页数:6
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