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Palabras clave – provistas por la editorial

iron; cross-coupling; aryl esters; C–O activation; Fe-catalysis; Kumada cross-coupling; iron complexes; hydrogen transfer; reductive amination; alcohols; amines; decarbonylation; alkylation; spirocyclization; aldehyde; cinnamamide; iron catalysis; bis-(aryl)manganese; alkenyl halides; ate iron(II) complex; asymmetric catalysis; nitrogen ligand; oxidative coupling; BINOL synthesis; carbene; diazoalkane; C-H functionalization; catalysis; borylation; Iron; C-H functionalisation; pinacolborane; photochemistry; amidation; iron(III) chloride; amides; esters; solvent-free; iron-catalysis; carboazidation; β-methyl scission; radical; DFT; organic synthesis; C-H activation; C-C coupling; α-alkenylation; dehydrogenative coupling; sustainability; naphthidines; fluorescence; iron catalyst; ATRP; controlled radical polymerization; external stimuli; asymmetric transfer hydrogenation; density functional theory; bifunctional catalyst; haloalkane coupling; Grignard reagent; FeI/FeII/FeIII mechanism