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A Theoretical Study on the Tautomerism of C-Carboxylic and Methoxycarbonyl Substituted Azoles
Authors:Ibon?Alkorta  author-information"  >  author-information__contact u-icon-before"  >  mailto:ibon@iqm.csic.es"   title="  ibon@iqm.csic.es"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,José?Elguero
Affiliation:(1) Instituto de Química Médica (C.S.I.C.), Juan de la Cierva, 3, E-28006 Madrid, Spain
Abstract:DFT calculations (B3LYP/6-31+G**) have been carried out on 106 tautomers and conformers of NH-azoles bearing CO2H and CO2CH3 groups. The following azoles systems have been studied: 2-substituted pyrroles, 2-substituted indoles, 2-substituted imidazoles, 2-substituted benzimidazoles, 4(5)-substituted imidazoles, 3(5)-substituted pyrazoles, 3-substituted indazoles (1H and 2H), 3,4(5)-substituted-1,2,3(5)-triazoles, 2,3(5)-substituted-1,2(3),4-triazoles, 4(5)-1,2,3,4(5)-tetrazoles. In the case of pyrazole, 3,5-disubstituted derivatives have also been computed, including four dimers.Dedicated to our friend Professor Vladimir I. Minkin on his 70th anniversary.
Keywords:DFT calculations  azoles  tautomerism  carboxylic acids  esters
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