N,N-Dimethylformamide’s Participation in Domino Reactions for the Synthesis of Se-Phenyl Dimethylcarbamoselenoate Derivatives
<i>N</i>,<i>N</i>-dimethylformamide's (DMF) participation in domino reactions has been developed. Starting from substituted halogenobenzenes and selenium powder, versatile biologically active Se-phenyl dimethylcarbamoselenoate derivatives were efficiently synthesized under mild reaction conditions. The reaction mechanism was studied using control experiments. These protocols involve a wider substrate scope and provide an economical approach toward C-selenium bond formation.
Authors
- Ning Yu (ORCID: https://orcid.org/0000-0003-1770-3151)
- Shanshan Hu (ORCID: https://orcid.org/0000-0003-4904-0583)
- Jin Xu (ORCID: https://orcid.org/0000-0002-6377-1190)
- Ruren Xu
- L. Eduardo Wu
Institutions
- Huzhou Normal University (CN)
Publication Details
- Journal
- Molecules
- Published
- 2025-02-06
- DOI
- https://doi.org/10.3390/molecules30030747
- Citations
- 1
- Primary Topic
- Sulfur-Based Synthesis Techniques
- Type
- article
- Field-Weighted Citation Impact
- 0.94