Journal2022
Transition-metal-catalyzed one-pot selenylation of electrophilic arylating agents using triphenyltin chloride/Se as a phenylselenating agent
Organic & Biomolecular Chemistry Vol. 20, No. 22, 4625–4634
چکیده
as a magnetically reusable nanocatalyst was applied in these reactions under similar reaction conditions. The present methods are superior to other currently available methods due to the use of triphenyltin chloride/Se as a phenylselenating agent and phenolic esters and nitroarenes as a coupling partner for C-Se-C bond formation for the first time, a green solvent and inexpensive and reusable catalysts, and avoidance of any toxic and expensive arylselenating reagents.
موضوعات و کلیدواژهها
Sulfur-Based Synthesis TechniquesOrganoselenium and organotellurium chemistryRadical Photochemical ReactionsChemistryElectrophileCatalysisArylReagentChlorideCombinatorial chemistryHalideSolventCoupling reactionTransition metalMedicinal chemistryOrganic chemistryAlkyl
ارجاع علمی
Zeinab Shirvandi, Bahareh Atashkar, Mohammad Ali Zolfigol, Amin Rostami. “Transition-metal-catalyzed one-pot selenylation of electrophilic arylating agents using triphenyltin chloride/Se as a phenylselenating agent.” Organic & Biomolecular Chemistry, 2022. https://doi.org/10.1039/d2ob00011c