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Free radical multicomponent reactions (MCR) aremore flexible and fulfillfor an efficient carbo-functionalizationof olefins1.Radical MCRs have thus attracted a considerableattention.More recently, the addition of carbonfragments across the π-bond of non-activated olefins throughfreeradical pathways has received intense scrutiny, resulting inthe description of useful transformations, such as for instancecarbo-alkenylation2,3, carboalkynylation4 andcarbo-allylationofolefins.These processes also illustrate the importance of theinfluence of polar effects in free-radical MCRs5. Various electrophilic species maybe envisioned, but sulfones including vinyl6-,alkynyl-,allyl7and azido-sulfones8hold a prominent place, due to the ORIENTAL JOURNAL OF CHEMISTRY

High Efficient of the Intermolecular Radical Reactions Through three-Component Carbo-Oximation Process using New Ready Available Sulfonyloxime