Angewandte Chemie International Edition · 2021 · 150 citations · 54 references
Natural SciencesChemistryMedicinal ChemistryCatalysisGreen ChemistryOrganic ChemistryCatalytic MechanismsPhotocatalysisPhotochemistryRadical ReactionsReaction Mechanism AnalysisReaction MechanismsChiral Carboxylic AcidsCopper-catalyzed CouplingEnantioselective OxidationEnantioselective SynthesisFunctional Group ToleranceMild Reaction ConditionsScopeTransition-metal-catalyzed Cross-coupling
Kharasch-Sosnovsky reaction is one of the most powerful methods for allylic oxidation of alkenes. However, the inherent radical mechanism and use of peroxides as both oxidants and oxygen nucleophiles render dearth of universal catalytic systems for highly enantioselective variants and limited scope. Herein, an alternative to the asymmetric Kharasch-Sosnovsky reaction that utilized a chiral copper catalyst and purple-LED irradiation to enable the three-component coupling of 1,3-dienes, oxime esters, and carboxylic acids is reported. This protocol features mild conditions, remarkable scope and functional group tolerance as evidenced by >80 examples and utility in the late-stage modification of pharmaceuticals and natural products. Detailed mechanistic studies provide evidences for the radical-based reaction pathway.
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Asymmetric copper-catalyzed C-N cross-couplings induced by visible light
Quirin M. Kainz, Carson D. Matier, Agnieszka Bartoszewicz et al. · Science · 2016 · 761 citations · Full text
Nitrile-containing natural products
Fraser F. Fleming, Fraser F. Fleming · Natural Product Reports · 1999 · 670 citations