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Drewson

BAEYER - DREWSON Indoxyl Synfhesis Conversion of o-nitrobenzaldehyde and ketones to indoxyls. [Pg.12]

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]

BAER FISCHER Ammo sugar synthesis 10 BAEYER Oxindolesynthesis It BAEYER Oiarylmethane synthesis 11 BAEYER Pyridine synthesis 12 BAEYER - DREWSON Indoxyt synthesis 12 BAEYER VILLIGER Ketone oxidation 13 BAEYER - VILLIGER Tntylation 13 BAKER - VENKATARAMAN Flavone synthesis t4... [Pg.223]

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]

DOEBNER - MILLER Quinoline synthesis 98 DOERING - LA FLAMME Aliens synthesa 99 DONDONI Homologation 100 DOTZ Hydroqumone synthesis 101 Drechset 123 Drewson 12... [Pg.224]

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

Other references related to the Baeyer-Drewson reaction are cited in the literature. [Pg.139]

See other pages where Drewson is mentioned: [Pg.12]    [Pg.15]    [Pg.155]    [Pg.307]    [Pg.127]    [Pg.10]    [Pg.224]    [Pg.10]    [Pg.10]    [Pg.322]    [Pg.307]    [Pg.56]    [Pg.136]    [Pg.136]    [Pg.136]    [Pg.138]    [Pg.139]    [Pg.139]    [Pg.1751]    [Pg.13]    [Pg.13]    [Pg.11]    [Pg.12]    [Pg.1]    [Pg.5]    [Pg.67]    [Pg.67]    [Pg.67]    [Pg.131]    [Pg.291]    [Pg.27]   
See also in sourсe #XX -- [ Pg.12 ]



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BAEYER - DREWSON Indoxyl synthesis

Baeyer-Drewson

Baeyer-Drewson indigo synthesis

The Baeyer-Drewson Synthesis of Indigo

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