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Pyrazolo pyrazole, tautomerism

The tautomeric equilibrium between IH- and 2//-formycin (7-amino-3)8-D-ribofuranosyl-l//-pyrazolo[4,3-d]pyrimidine) has a constant ratio N(2)H/N(1)H = 0.2 and an enthalpy difference estimated at 1 kcal mol". The tautomeric interconversion is catalyzed by (3 x 10 Msec" ) and by OH" (5 X 10 M" sec" ). No other catalytic pathway such as water catalysis or tautomerization via tautomeric cations contributes significantly to the interconversion. Protonation on the pyrazole ring of formycin does not occur significantly (80JA3897). [Pg.366]

AMI semiempirical calculations have shown that, as far as tautomerism is concerned, there is a structural relationship between jS-dicarbonyl compounds and NH-pyrazoles, and in a wide variety of NH-pyrazoles studied " the most stable tautomer was found to be that having the largest single-bond character between the C(3)—C(4) bond. The problem of proton transfer in NH-pyrazole crystals has been subjected to a detailed theoretical study, while a study of the tautomerism of 2-aryl and 2-heteroaryl derivatives of benzimidazole has indicated that tautomerism takes place by the intermolecular relay of protons between stacked molecules. The first report of the stable co-existence of two different histidine tautomers in one peptide crystal structure has appeared. Ab initio calculations have been used to study the tautomerism of both histamine and pyrazolo[3,4-i/]pyridazine in the gas phase and in aqueous solution, and a theoretical study of the NH tautomerism in free-base porphyrin has been undertaken. ... [Pg.589]

H-Pyrazolo[ 1,2-u]pyrazol-4-ium chloride, 2,3,6,7-tetrahydro-synthesis, 6, 1012 Pyrazolopyridazines synthesis, 5, 322, 326 tautomerism, 5, 309 Pyrazolo[ 1,2-a]pyridazines hydrogenation, 5, 328 reactions... [Pg.778]

The C n.m.r. spectra of formycin, formycin B, and certain pyrazolo[4,3-f/]-pyrimidines have been examined in DMSO and HMPT, and as a function of temperature, in order to probe the prototropic tautomerism of the pyrazole portion of the heterocyclic system. Only the 1-NH % 2-NH prototropic process was observed, and the proportion of the 2-NH tautomer (a higher energy species than the 1-NH tautomer) was shown to depend on the substituent present at C-7 of the pyrimidine portion of the heterocyclic system. [Pg.170]

Acylation and metallation studies on monomers, dimers, trimers, and tetramers containing linked thiophen, pyridine, pyrimidine, furan, benzofuran, benzothiophen, and indole moieties have been published/ Deuteriation, halogenation, and diazo-coupling reactions of 2-oxo- and 2-thioxo-l,2-dihy-dropyrimidinium salts have been studied and compared with results for 2,2-dialkyl-1,2-dihydropyrimidinium and 2,3-dihydro-1,4-diazepinium salts in order to demonstrate the effect of an adjacent 0x0- or thioxo-group on the properties of a 1,5-diazopentadienium system/ Vilsmeier formylation of, and tautomerism in, 2-hydroxypyrazolo[5,l-h]quinazolone and l-phenylpyrazolo[5,l-A]-quinazoline-2,9-dione have been studied/ The pyrazolo[3,4-c]pyrazole (71) has been methylated and acetylated, the major products being (72)/ ... [Pg.283]


See other pages where Pyrazolo pyrazole, tautomerism is mentioned: [Pg.778]    [Pg.84]    [Pg.374]    [Pg.778]    [Pg.589]    [Pg.589]    [Pg.84]    [Pg.778]    [Pg.676]    [Pg.137]    [Pg.84]   
See also in sourсe #XX -- [ Pg.77 , Pg.88 ]

See also in sourсe #XX -- [ Pg.77 , Pg.88 ]




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