Copper-Catalyzed Sulfinyl Cross-Coupling Reaction of Sulfinamides

被引:4
|
作者
Kou, Mengting [1 ]
Wei, Ziqiang [1 ]
Li, Zhen [1 ]
Xu, Bin [1 ,2 ]
机构
[1] Shanghai Univ, Innovat Drug Res Ctr, Peoples Hosp Nantong 6, Affiliated Nantong Hosp,Shanghai Engn Res Ctr Orga, Shanghai 200444, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
ASYMMETRIC-SYNTHESIS; SULFOXIDES; LIGANDS; ANTIBACTERIAL; ACTIVATION; ALCOHOLS; AMIDES;
D O I
10.1021/acs.orglett.2c03414
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A copper-catalyzed sulfinyl cross-coupling reaction of sulfinamides with aldehyde-derived N-tosylhydrazones is described. This approach enables facile access for the construction of structurally diverse sulfoxides via novel and efficient S-N/S-C bond interconversions, features broad substrate scope, and accommodates various functional groups as well as pharmacophores. Moreover, the given sulfinyl cross-coupling reaction could be scaled up to the gram scale and carried out in a one-pot fashion directly from aldehydes. The broad utility of produced sulfoxides is demonstrated by further transformations. A preliminary mechanistic investigation was performed, which disclosed possible reaction pathways.
引用
收藏
页码:8514 / 8519
页数:6
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