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Amino compounds indole, reduction

Curtius rearrangement of the heteroaroyl azides, obtained from the reaction of the carboxylic acid chlorides with sodium azide, provides a route to the amino-pyrroles and -indoles (e.g. B-70MI30504, B-77MI30506, 78CPB1054), which, because of the ease of synthesis of the carboxylic acids, is frequently preferable to reduction of the nitro compounds. [Pg.288]

See other pages where Amino compounds indole, reduction is mentioned: [Pg.995]    [Pg.205]    [Pg.7]    [Pg.211]    [Pg.44]    [Pg.714]    [Pg.8]    [Pg.194]    [Pg.171]    [Pg.48]    [Pg.256]    [Pg.106]    [Pg.317]    [Pg.362]    [Pg.142]    [Pg.1498]    [Pg.317]    [Pg.362]    [Pg.304]    [Pg.316]    [Pg.56]    [Pg.23]    [Pg.48]    [Pg.506]    [Pg.86]    [Pg.434]    [Pg.436]    [Pg.230]    [Pg.329]    [Pg.491]    [Pg.724]    [Pg.431]    [Pg.198]   
See also in sourсe #XX -- [ Pg.186 ]



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Amino compounds

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Indole, reduction

Indoles compounds

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