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Reduction Reimer—Tiemann reaction

Pinacol-pinacolone rearrangement Prileschajew epoxidation reaction Reformatsky reaction Reimer-Tiemann reaction Rosemnund reduction Sandmeyer reaction Schiemann reaction Schmidt reaction or rearrangement Schotten-Baumann reaction Skraup reaction Sommelet reaction. ... [Pg.10]

The Reimer-Tiemann reaction is not an effective route to formyl-pyrroles or -indoles (see Section 3.05.1.6) and the oxidation of alkyl and hydroxyalkyl derivatives of the heterocycles and the reduction of carboxylic acid derivatives are discussed in Sections 3.05.2.2 and 3.05.2.4, respectively. [Pg.224]

Redox equations, balancing, 265 Reduction of aromatic compounds, 200 Reductive amination, 404 Reductive hydroboration, 95 Reformatsky reaction, 321 Regioselective reactions, 97 Reimer-Tiemann reaction, 438 Resonance, 23 in benzene, 192 energy, 24 structures, 29 Resorcinol, 327, 432 Retroaldol condensation, 399 Ring activation, 2(fiff Robinson inaction, 398 Rosenmund reduction, 306... [Pg.468]


See other pages where Reduction Reimer—Tiemann reaction is mentioned: [Pg.19]    [Pg.551]    [Pg.791]    [Pg.820]    [Pg.551]    [Pg.671]    [Pg.791]    [Pg.820]    [Pg.866]    [Pg.642]    [Pg.671]    [Pg.791]    [Pg.820]    [Pg.2635]    [Pg.60]    [Pg.551]    [Pg.671]    [Pg.791]   
See also in sourсe #XX -- [ Pg.95 , Pg.98 , Pg.220 , Pg.256 , Pg.269 ]




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