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Electrophilic amination

Solvent-free conditions were used by Tanaka et al. in their assays to obtain intermolecular reactions from alkynes and anilines. The chosen catalyst was [AuMe(PPh3)] with an acidic promoter [92]. Reaction, whose effectiveness was greater in the case of aromatic amines, proceeded via Markovnikov by amine electrophilic attack of the alkyne in a similar way to the methanol addition proposed by Teles (see Section 2.1.3.2) and provided high yields and TONs. [Pg.459]

Cbz(Z) (OCOBn) 0 amines electrophiles BnOCOCl, base HBr, AcOH,orH2, Pd... [Pg.657]

Fmoc fl uoroe ny loxycarbony 1 see text amines electrophiles, Fmoc-CI base, e.g. amine... [Pg.657]

See other pages where Electrophilic amination is mentioned: [Pg.1045]    [Pg.654]    [Pg.654]    [Pg.653]    [Pg.657]    [Pg.656]    [Pg.657]    [Pg.656]    [Pg.657]    [Pg.24]    [Pg.260]    [Pg.335]    [Pg.656]    [Pg.657]    [Pg.557]    [Pg.559]    [Pg.560]    [Pg.560]    [Pg.105]    [Pg.106]    [Pg.2143]    [Pg.342]    [Pg.251]    [Pg.279]    [Pg.50]   
See also in sourсe #XX -- [ Pg.550 , Pg.551 , Pg.552 ]

See also in sourсe #XX -- [ Pg.575 , Pg.576 , Pg.577 , Pg.578 , Pg.579 ]

See also in sourсe #XX -- [ Pg.550 , Pg.551 , Pg.552 ]

See also in sourсe #XX -- [ Pg.6 , Pg.119 ]

See also in sourсe #XX -- [ Pg.119 ]

See also in sourсe #XX -- [ Pg.6 , Pg.119 ]

See also in sourсe #XX -- [ Pg.119 ]



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Electrophilic aminations

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