Copper catalyzed N-arylation of sulfoximines with aryldiazonium salts in the presence of DABCO under mild conditions
| dc.contributor.author | Baranwal S.; Kandasamy J. | |
| dc.date.accessioned | 2025-05-23T11:30:12Z | |
| dc.description.abstract | N-Arylation of sulfoximines with aryldiazonium tetrafluoroborates is demonstrated in the presence of copper chloride and DABCO. A wide range of aryl and alkyl sufoximines are participated in the coupling reaction with different aryldiazonim salts bearing electron donating and withdrawing groups and provided the desired products in 67–88% yields. The reaction proceeds through a radical mechanism. © 2020 Elsevier Ltd | |
| dc.identifier.doi | https://doi.org/10.1016/j.tetlet.2020.152079 | |
| dc.identifier.uri | http://172.23.0.11:4000/handle/123456789/11914 | |
| dc.relation.ispartofseries | Tetrahedron Letters | |
| dc.title | Copper catalyzed N-arylation of sulfoximines with aryldiazonium salts in the presence of DABCO under mild conditions |