作者:Mengting Kou、Ziqiang Wei、Zhen Li、Bin Xu
DOI:10.1021/acs.orglett.2c03414
日期:2022.11.25
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
描述了亚磺酰胺与醛衍生的N-甲苯磺酰腙的铜催化亚磺酰交叉偶联反应。这种方法能够通过新颖高效的 S-N/S-C 键互变轻松构建结构多样的亚砜,具有广泛的底物范围,并适应各种官能团和药效团。此外,给定的亚磺酰基交叉偶联反应可以放大到克级,并直接从醛类以一锅法进行。进一步的转化证明了所产生的亚砜的广泛用途。进行了初步的机理研究,揭示了可能的反应途径。