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3-Acetyloxindole

Acetyloxindole, 40, 1 Aud chlorides, from acids and chloro vmylamuies, 41, 23 from cyanoacetic acid, 41, 5 from pentaacetylglucomc acid, 41, 80 Acrylamide, N benzyl, 42,16 Acrylonitrile, reaction with benzyl alcohol, 42, 16... [Pg.105]

Potassium amide in conversion of o-acetoacetochloroanilide to 3-acetyloxindole, 40, 1 Potassium tert-butoxide, 41, 101 in dehydration of formamides to isocyanides, 41, 101... [Pg.64]

Acetyloxindole, 909 S-Acetylpantetheine, 379,1157 Acetylpyrrole, 2- and 3-, 13 N-Acetylpyrrole, 13 Acetylsalicylic acid, 338 3-0-Acetylstrophanthidin, 622 3-O-Acetylstrophanthidol, 622... [Pg.697]

Generation of a bernyne intermediate. A general principle of synthesis devised by Bunnett involves creation of an intermediate benzyne having a nucleophilic center so located that it can add intramolecularly to the triple bond. An example is the synthesis of 3-acetyloxindole from o-chloroacetoacetanilide (Union Carbide Chem. Co.) with potassium amide in liquid ammonia. In another synthesis o- and m-halo isomers gave the same product. [Pg.1188]

Cyclization, of o-acetoacetochloroanilide to 3-acetyloxindole, 1 polyphosphoric acid in, 43 Cyclohexanone in preparation of methylene cyclohexane, 66 2-Cyclohexenone, 14... [Pg.56]

See other pages where 3-Acetyloxindole is mentioned: [Pg.3]    [Pg.4]    [Pg.4]    [Pg.4]    [Pg.57]    [Pg.56]    [Pg.59]    [Pg.105]    [Pg.56]    [Pg.55]    [Pg.3]    [Pg.3]    [Pg.3]    [Pg.62]    [Pg.63]   
See also in sourсe #XX -- [ Pg.40 ]

See also in sourсe #XX -- [ Pg.40 ]

See also in sourсe #XX -- [ Pg.40 ]

See also in sourсe #XX -- [ Pg.40 ]

See also in sourсe #XX -- [ Pg.40 ]

See also in sourсe #XX -- [ Pg.40 ]



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O-Acetoacetochloranilide, reaction with yield 3-acetyloxindole

Potassium amide in conversion 3-acetyloxindole

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