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Ketodicarboxylic acid

Decarboxylation of /3-ketodicarboxylic acids - approximations to the overall rate expression deduced from the mechanism, 341-342 Decarboxylation of oxaloacetic acid - contributions to the overall rate, 342-343 Glycine ethyl ester, metal ion catalysed hydrolysis, formulation of the rate expression, 344-346... [Pg.444]

Arylimines can be obtained by the addition of N-silylated amides to aryl-lithium compounds (Scheme 200) 44 the imines may be isolated or reduced in situ to amines, or hydrolysed to carbonyl compounds. a-Ketodicarboxylic acid chloride imine chlorides, which readily undergo cyclization to N-heterocycles, have been prepared by -addition of dicarboxylic acid chlorides to isocyanides (Scheme 201).444 Two new formimidoylamino-substituted carbapenems (4) have been prepared by a route involving a hetero Diels-Alder reaction (Scheme 4).14... [Pg.365]

C. Triketones, Ketodialdehydes (Oxoglutaconaldehydes), and Ketodicarboxylic Acid Derivatives... [Pg.608]

Ketodialdehydes (oxoglutacon-aldehyde), 608 Ketodicarboxylic acids, 608 Ketoenaxnines, cyclization to 4-pyridonas, 610 g-Ketoesters, 601, 619 cyclization with, cyanoaceta-inide, 625... [Pg.1227]

A 3-carbon ketodicarboxylic acid an intermediate in the Krebs cycle. [Pg.823]

See other pages where Ketodicarboxylic acid is mentioned: [Pg.203]    [Pg.263]    [Pg.261]    [Pg.261]    [Pg.322]    [Pg.314]    [Pg.272]    [Pg.327]    [Pg.251]    [Pg.248]    [Pg.271]    [Pg.203]    [Pg.263]    [Pg.261]    [Pg.261]    [Pg.322]    [Pg.314]    [Pg.272]    [Pg.327]    [Pg.251]    [Pg.248]    [Pg.271]   


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