Ring-opening iodination and bromination of unstrained cycloalkanols through β-scission of alkoxy radicals
Jiang‐Ling Shi, Yuankai Wang, Zixuan Wang, Bowen Dou, Jianbo Wang
Abstract
), thus significantly avoiding undesired side reactions. The reaction is under mild conditions and has a wide substrate scope, thus providing a practically useful method for accessing ω-iodo or ω-bromoketones.
Topics & Concepts
HalogenationTriiodideChemistryBond cleavageAlkoxy groupPhotochemistryRing (chemistry)Substrate (aquarium)RadicalMedicinal chemistryCleavage (geology)Organic chemistryAlkylCatalysisMaterials sciencePhysical chemistryFracture (geology)ElectrodeComposite materialOceanographyElectrolyteDye-sensitized solar cellGeologyVanadium and Halogenation ChemistryOxidative Organic Chemistry ReactionsRadical Photochemical Reactions