Escobar, Randolph A.; Johannes, Jeffrey W. published their research in Organic Letters in 2021. The article was titled 《Reductive Radical Conjugate Addition of Alkyl Electrophiles Catalyzed by a Cobalt/Iridium Photoredox System》.Safety of 4-Bromotetrahydropyran The article contains the following contents:
A reductive radical conjugate addition that allowed the formation of alkyl radicals via activation of alkyl bromides through cobalt/iridium catalysis was reported. The developed conditions were emphasized in the broad substrate scope presented, including benzylic halides and halides containing free alcs., silanes and chlorides. The experimental process involved the reaction of 4-Bromotetrahydropyran(cas: 25637-16-5Safety of 4-Bromotetrahydropyran)
4-Bromotetrahydropyran(cas: 25637-16-5) is often used as reactant for: nickel-catalyzed alkyl-alkyl Suzuki coupling reactions with boron reagents, preparation of a selective small-molecule melanocortin-4 receptor agonist with efficacy in a pilot study of sexual dysfunction in humans; preparation of aliphatic hydrocarbons via nickel-catalyzed Suzuki cross-coupling with alkylboranes.Safety of 4-Bromotetrahydropyran
Referemce:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics