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Azides, aryl reactions with organoboranes

Organoboranes react with a mixture of aqueous NH3 and NaOCl to produce primary amines. It is likely that the actual reagent is chloramine NH2CI. Chloramine itself,hydroxylamine-O-sulfonic acid in diglyme, and trimethyl-silyl azide " also give the reaction. Since the boranes can be prepared by the hydroboration of alkenes (15-16), this is an indirect method for the addition of NH3 to a double bond with anti-Markovnikov orientation. Secondary amines can be prepared by the treatment of alkyl- or aryldichloroboranes or dialkylchlorobor-anes with alkyl or aryl azides. [Pg.800]


See other pages where Azides, aryl reactions with organoboranes is mentioned: [Pg.24]    [Pg.326]   
See also in sourсe #XX -- [ Pg.607 ]

See also in sourсe #XX -- [ Pg.607 ]

See also in sourсe #XX -- [ Pg.7 , Pg.607 ]

See also in sourсe #XX -- [ Pg.7 , Pg.607 ]

See also in sourсe #XX -- [ Pg.607 ]




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Aryl azides reactions

Azidation reaction

Azides organoboranes

Azides reactions with organoboranes

Azides, reactions

Organoborane

Organoborane reactions

Organoboranes

Organoboranes, reactions

Reaction with azide

With Azides

With organoboranes

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