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An Update on Distal C(<i>sp</i><sup><i>3</i></sup>)−H Functionalization Involving 1,5‐HAT Emerging from Nitrogen Radicals
30
Citations
46
References
2020
Year
EngineeringMolecular BiologyOrganic ChemistryChemistryRedox BiologyReactive Nitrogen SpecieC−h BondReaction IntermediateSp 3BiochemistryChemical BondRadical (Chemistry)Diversity-oriented SynthesisMolecular ChemistryFunctionalization Involving 1,5‐HatBiomolecular EngineeringNatural SciencesDistal CRadical ReactionsNitrogen RadicalsNitrosative Stress
Abstract Methods to selectively functionalize any one sp 3 C−H bond among all others, has been well documented in literature. Radical reactions, which are essentially mild reaction conditions has provided a significant improvement over the standard functionalization pathways. Although radical recombinations are fast and feasible, the selectivity is always guided by the electronic biasness in the system. 1,n‐Hydrogen atom transfer (HAT) reactions are extremely useful in determining regioselectivity, the involvement of a 1,5‐HAT protocol made the reaction pathway energetically much more favourable to functionalize the desired remote C( sp 3 )−H bond. In this review we are going to give a brief overview of the methods involved in the functionalization of distal aliphatic C−H bond by 1,5‐HAT transformation pathway.
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