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Pyridine dicarboxylate

Pyridine 210 is oxidized by 20% nitric acid at the acetyl group to 2-methyl-5-pyridinecarboxylic acid, while its ozonation gives cinchomeronic acid [pyridine-2,5-dicarboxylic acid (215)] (75DIS) which is decarboxylated (200°C, 2 h) to nicotinic acid 216 in 97% yield (75DIS). [Pg.212]

Cyclohexaamylose continued) mono-6-O-tosyl-, preparation of, 23 250 pyridine-2,5-dicarboxylic acid derivative, catalytic action of, 23 251 separation of, by complexing, 23 214 structure, stereochemistry and physical properties of, 23 210-213... [Pg.85]

Reaction of the m-nitrophenyl ester of pyridine-2,5-dicarboxylic acid with cyclodextrin (see Section 3) gives a picolinate ester [52] of a cyclodextrin secondary hydroxyl group (Breslow, 1971 Breslow and Overman, 1970) which will bind metal ions or a metal ion-pyridine carboxaldoxime complex. Such a complex will catalyse hydrolysis of p-nitrophenyl acetate bound within the cyclodextrin cavity leading to a rate constant approximately 2000-fold greater at... [Pg.71]

Pyridine-2,5-dicarboxylic acid [100-26-5] M 167.1, m 254 . Crystd from dilute HCI. Pyridine-2,6-dicarboxylic acid see dipicolinic acid. [Pg.318]

The problem was resolved essentially by stepwise degradation of the molecule to furan-3-carboxylic acid, pyridine-2,5-dicarboxylic acid (V), nupharidinic acid (XVIII), and anhydronupharanediol, C15H30O (XV), with the structure of the last-named supplying the key to that of deoxynupharidine (15, 16). Chart I show s the main steps of the degradation. [Pg.446]

When dehydrogenated on palladium the hexahydroderivative IV afforded C15H23ON which could be converted to pyridine-2,5-dicarboxylic acid (V) by oxidation with permanganate (13, 18, 19). [Pg.446]

Pyridine-2,5-dicarboxylic acid (isocinchomeronic acid) (C H.O.N) 700M... [Pg.459]

Pyridinedicarboxylic acid CAS 100-26-5 EINECS/ELINCS 202-834-2 Synonyms Isocinchomeronic acid 2,5-Pyridinedicarboxylic acid Pyridine-2,5-dicarboxylic acid Classification Organic compd. [Pg.3788]


See other pages where Pyridine dicarboxylate is mentioned: [Pg.829]    [Pg.344]    [Pg.189]    [Pg.251]    [Pg.184]    [Pg.153]    [Pg.153]    [Pg.113]    [Pg.465]    [Pg.344]    [Pg.406]    [Pg.179]    [Pg.197]    [Pg.459]    [Pg.478]    [Pg.478]    [Pg.6]    [Pg.30]    [Pg.331]    [Pg.2419]    [Pg.588]    [Pg.606]    [Pg.238]    [Pg.34]    [Pg.43]    [Pg.505]   
See also in sourсe #XX -- [ Pg.181 ]




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2,3-Pyridine dicarboxylic anhydride)

2,6-Dicarboxylate pyridine, complexes

2,6-pyridine dicarboxylate ligands

Dimethyl pyridine-2,3-dicarboxylate

Eluant pyridine-2,6-dicarboxylic acid

Eluant tartaric acid/pyridine-2,6-dicarboxylic

Eluents pyridine-2,6-dicarboxylic acid

Eluents pyridine-2,6-dicarboxylic acid/oxalic

Eluents pyridine-2,6-dicarboxylic acid/tartaric

Esters of pyridine-2,6-dicarboxylic acid

Pyridine dicarboxylates

Pyridine dicarboxylates

Pyridine dicarboxylates oxidation

Pyridine-2,3 -dicarboxylic acid reaction with

Pyridine-2,3-dicarboxylates, synthesis from

Pyridine-2,6-dicarboxylate , transition

Pyridine-2,6-dicarboxylic add

Pyridine-3,5-dicarboxylic acid esters

Pyridine-3,5-dicarboxylic acid hydrogenation

Pyridine-3,5-dicarboxylic acid, 1,4-dihydrohydride donors

Pyridine-3,5-dicarboxylic acid, reaction

Pyridine-3,5-dicarboxylic acid, reaction complexes

Pyridine-3,5-dicarboxylic acids

Pyridine-3,5-dicarboxylic ester, 1,4-dihydro

Pyridines pyridine-3,5-dicarboxylate

Pyridines pyridine-3,5-dicarboxylate

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