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Sodium tetracarbonylhydridoferrate

Reductionof imidoyl chlorides (1) toimines (2) andamines (J). This reaction can be conducted with sodium tetracarbonylhydridoferrate at 0-25°. Use of excess reagent permits conversion of 2 to 3. The paper presents a possible mechanism. [Pg.524]

Sodium hydrogen carbonate, 457 Sodium hydrogen selenide, 459 Sodium hydrogen telluride, 459-460 Sodium hydrosulfite, 252 Sodium hydroxide, 460-461 Sodium methoxide, 463 Sodium p-methoxythiophenoxide, 421 Sodium 2-mcthyl-2-butoxide, 339 Sodium naphthalenide, 464 Sodium nitronates, 370, 371 Sodium selenophenolate, 212, 307, 397 Sodium sulfide, 360 Sodium tetracarbonylhydridoferrate, 419-420... [Pg.304]

See other pages where Sodium tetracarbonylhydridoferrate is mentioned: [Pg.295]    [Pg.301]    [Pg.352]    [Pg.315]    [Pg.243]    [Pg.519]    [Pg.519]    [Pg.295]    [Pg.301]    [Pg.352]    [Pg.315]    [Pg.243]    [Pg.519]    [Pg.519]    [Pg.375]    [Pg.783]    [Pg.729]    [Pg.581]    [Pg.163]   
See also in sourсe #XX -- [ Pg.295 ]

See also in sourсe #XX -- [ Pg.352 ]

See also in sourсe #XX -- [ Pg.315 ]



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Tetracarbonylhydridoferrates

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