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

Ruren Xu,

Shanshan Hu,

L. Eduardo Wu

et al.

Molecules, Journal Year: 2025, Volume and Issue: 30(3), P. 747 - 747

Published: Feb. 6, 2025

N,N-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 mechanism was studied using control experiments. These protocols involve a wider substrate scope provide an economical approach toward C–selenium bond formation.

Language: Английский

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

Ruren Xu,

Shanshan Hu,

L. Eduardo Wu

et al.

Molecules, Journal Year: 2025, Volume and Issue: 30(3), P. 747 - 747

Published: Feb. 6, 2025

N,N-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 mechanism was studied using control experiments. These protocols involve a wider substrate scope provide an economical approach toward C–selenium bond formation.

Language: Английский

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