Search results for "Fe-catalysis"

showing 2 items of 2 documents

Iron-Catalyzed Cross-Coupling Reactions of Alkyl Grignards with Aryl Chlorobenzenesulfonates

2021

Aryl sulfonate esters are versatile synthetic intermediates in organic chemistry as well as attractive architectures due to their bioactive properties. Herein, we report the synthesis of alkyl-substituted benzenesulfonate esters by iron-catalyzed C(sp2)–C(sp3) cross-coupling of Grignard reagents with aryl chlorides. The method operates using an environmentally benign and sustainable iron catalytic system, employing benign urea ligands. A broad range of chlorobenzenesulfonates as well as challenging alkyl organometallics containing β-hydrogens are compatible with these conditions, affording alkylated products in high to excellent yields. The study reveals that aryl sulfonate esters are the m…

Pharmaceutical ScienceAlkylationArticleCoupling reactionAnalytical ChemistryCatalysischemistry.chemical_compoundironQD241-441Drug Discoverycross-couplingOrganic chemistryPhysical and Theoretical ChemistryAlkylchemistry.chemical_classificationChemistryArylOrganic ChemistrySulfonateChemistry (miscellaneous)Fe-catalysisReagentUreaKumada cross-couplingMolecular MedicineC–O activationaryl sulfonatesMolecules
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Iron-Catalyzed C(sp2)–C(sp3) Cross-Coupling of Aryl Chlorobenzoates with Alkyl Grignard Reagents

2020

Aryl benzoates are compounds of high importance in organic synthesis. Herein, we report the iron-catalyzed C(sp2)&ndash

Chlorobenzoatesaryl estersPharmaceutical ScienceMedicinal chemistryArticleCatalysisAnalytical ChemistryCatalysislcsh:QD241-441chemistry.chemical_compoundironlcsh:Organic chemistryDrug Discoverycross-couplingPhysical and Theoretical ChemistryAlkylchemistry.chemical_classificationNucleophilic additionMolecular StructureArylOrganic ChemistryBenzoatesChlorobenzoateschemistryChemistry (miscellaneous)Fe-catalysisFunctional groupKumada cross-couplingMolecular MedicineOrganic synthesisC–O activationIron CompoundsMolecules
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