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

и другие.

Molecules, Год журнала: 2025, Номер 30(3), С. 747 - 747

Опубликована: Фев. 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.

Язык: 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

и другие.

Molecules, Год журнала: 2025, Номер 30(3), С. 747 - 747

Опубликована: Фев. 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.

Язык: Английский

Процитировано

0