INDO MO calculations of the electronic structures of pyrolle, imidazole, and derivatives
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry
Reference63 articles.
1. The σ−and π−inductive effects
2. The Nature and Analysis of Substituent Electronic Effects
3. Valence shell calculations on polyatomic molecules. II. Complete neglect of differential overlap-self-consistent field calculations on monosubstituted benzenes
4. Infrared intensities as a quantitative measure of intramolecular interactions. XIII. Molecular orbital calculations of the intensities of ring-stretching bands of substituted benzenes
5. Molecular orbital theory of the electronic structure of organic compounds. XII. Conformations, stabilities, and charge distributions in monosubstituted benzenes
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1. Physical and Theoretical Aspects of 1H-Pyrroles;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02
2. Synthesis, acidity and 19F NMR characteristics of imidazoles bearing 1-fluorinated substituents with potential application as probes for intracellular pH determination;Tetrahedron;1997-06
3. Kinetics and mechanism of the imidazole-catalysed hydrolysis of substitutedN-benzoylimidazoles;Journal of Physical Organic Chemistry;1994-08
4. Ab initioSCF MO calculations on the reactions of hydroxyl radical with imidazole and monoprotonated imidazole;Journal of Computational Chemistry;1985-02
5. Electronic spectra and excited state dipole moments of heterocyclic pentaatomic systems and their benzo and dibenzo derivatives;Journal of Molecular Structure: THEOCHEM;1983-06
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