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Baeyer-Drewson indigo synthesis

Sainsbury, M. In Rodd s Chemistry of Carbon Compounds IVB, 1977, 346. (Review). [Pg.15]

The most electron-rich alkyl group (more substituted carbon) migrates first. The general migration order tertiary alkyl secondary alkyl cyclohexyl benzyl phenyl primary alkyl methyl H [Pg.16]

Beckmann, O. Compr. Asymmetric Catal. Till 1999, 2, 803. (Review). [Pg.16]

Baeyer-Drewson indigo synthesis. Formation of indigos by an aldol addition of o-nitrobenzal-dehydes to acetone, pymvic acid, or acetaldehyde. Of interest mainly as a method of protecting o-nitro-benzaldehydes. [Pg.117]

Propose the mechanism of the Baeyer-Drewson indigo synthesis. [Pg.112]

The classical Baeyer-Drewson synthesis of indigo 1 consists of reaction of o-nitrobenzaldehyde with acetone in the presence of aqueous sodium hydroxide. [Pg.127]

See other pages where Baeyer-Drewson indigo synthesis is mentioned: [Pg.15]    [Pg.307]    [Pg.307]    [Pg.56]    [Pg.136]    [Pg.1751]    [Pg.13]    [Pg.13]    [Pg.1]    [Pg.5]    [Pg.67]    [Pg.67]    [Pg.27]    [Pg.14]    [Pg.11]    [Pg.13]    [Pg.15]    [Pg.307]    [Pg.307]    [Pg.56]    [Pg.136]    [Pg.1751]    [Pg.13]    [Pg.13]    [Pg.1]    [Pg.5]    [Pg.67]    [Pg.67]    [Pg.27]    [Pg.14]    [Pg.11]    [Pg.13]    [Pg.136]    [Pg.155]    [Pg.127]    [Pg.11]   
See also in sourсe #XX -- [ Pg.307 ]

See also in sourсe #XX -- [ Pg.307 ]

See also in sourсe #XX -- [ Pg.56 ]

See also in sourсe #XX -- [ Pg.14 ]

See also in sourсe #XX -- [ Pg.11 ]



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