Chemodivergent Synthesis of Sulfonamide and Sulfones from N-Tosylhydrazones by Switching Catalyst and Temperature

被引:4
|
作者
Jin, Jingru [1 ,2 ]
Li, Chunyan [1 ,2 ]
Wang, Rui [1 ,2 ]
Xia, Zhimin [1 ,2 ]
Yan, Qiongjiao [1 ]
Wang, Wei [1 ]
Gu, ShuangXi [1 ,2 ,3 ]
Wang, Haifeng [1 ,2 ,3 ]
Chen, Fener [1 ,4 ,5 ]
机构
[1] Wuhan Inst Technol, Pharmaceut Res Inst, Wuhan 430205, Peoples R China
[2] Wuhan Inst Technol, Sch Chem Engn & Pharm, Wuhan 430205, Peoples R China
[3] Minist Educ, Key Lab Green Chem Engn Proc, Wuhan 430205, Peoples R China
[4] Fudan Univ, Dept Chem, Engn Ctr Catalysis & Synth Chiral Mol, Shanghai 200433, Peoples R China
[5] Shanghai Engn Ctr Ind Catalysis Chiral Drugs, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
REGIOSELECTIVE SYNTHESIS; SULFONYLATION; ANNULATIONS; HYDRAZONES; CARBONATES; PROGRESS;
D O I
10.1021/acs.orglett.3c02151
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A catalyst- and temperature-controlled selective synthesisof sulfonamideand sulfones from N-tosylhydrazones and MBH carbonateshas been developed. The use of palladium catalysts exclusively leadsto sulfonamide products at room temperature, whereas the selectivesynthesis of sulfones is dominant for a temperature-controlled couplingreaction without palladium catalysis. Importantly, the catalyst- ortemperature-controlled reaction exhibits high nucleophilicity ratherthan carbene reactivity in these transformations.
引用
收藏
页码:6012 / 6017
页数:6
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