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.

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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
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article

N,N-Dimethylformamide’s Participation in Domino Reactions for the Synthesis of Se-Phenyl Dimethylcarbamoselenoate Derivatives

Ning Yu, Shanshan Hu, Jin Xu, Ruren Xu et al.
1 citations
Molecules
Sulfur-Based Synthesis Techniques
0.94
article

N,N-Dimethylformamide’s Participation in Domino Reactions for the Synthesis of Se-Phenyl Dimethylcarbamoselenoate Derivatives

Ning Yu, Shanshan Hu, Jin Xu, Ruren Xu, L. Eduardo Wu
article en
1 citations

Abstract

<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.

MoleculesVol. 30(3)
Huzhou Normal University (CN)
Openalex Percentile: Top 29%
Sulfur-Based Synthesis Techniques
0.94
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