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Potassium hydridotetracarbonylferrate

N,N-Dialkylation of primary amines. Primary amines can be dialkylated by the reaction with an aldehyde and potassium hydridotetracarbonylferrate in ethanol under carbon monoxide at 20. ... [Pg.484]

N-ALKYLATION Lithium aluminum hydride. Potassium hydridotetracarbonylferrate. [Pg.777]

DEHALOGENATION l,8-Bis(dimethylamino)napthalene. Lithium diphenylphosphide. Potassium hydridotetracarbonylferrate. Sodium-t-Butanol-Tetrahydrofurane. Sodium borohydride. Sodium iodide. Tri- -butyltin hydride. [Pg.779]

DESULFURIZATION Hexamethylphosphorous triamide. Potassium hydridotetracarbonylferrate. Triethyl phosphite. [Pg.779]

Alkylation of carbonyl compounds. The reaction of a carbonyl compound, an aldehyde, and potassium or sodium hydridotetracarbonylferrate in a 1 1 1 molar ratio results in alkylation of the carbonyl compound (equation 1). [Pg.485]

See other pages where Potassium hydridotetracarbonylferrate is mentioned: [Pg.483]    [Pg.484]    [Pg.780]    [Pg.343]    [Pg.245]    [Pg.483]    [Pg.484]    [Pg.780]    [Pg.343]    [Pg.245]    [Pg.131]   
See also in sourсe #XX -- [ Pg.483 , Pg.484 , Pg.485 ]



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