A theoretical study of the relative stability of prototropic and acylotropic tautomers
β Scribed by B. Ya. Simkin; M. Ts. Zelenyi
- Publisher
- SP MAIK Nauka/Interperiodica
- Year
- 1981
- Tongue
- English
- Weight
- 226 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0022-4766
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π SIMILAR VOLUMES
The harmonic frequencies, IR intensities and the potential energy distributions of the vibrational modes of the keto and enol tautomers of guanine are calculated at the Hartree-Fock 6-31G\*\* level. The results are compared with the experimental spectra obtained in an argon low temperature matrix. E
## Abstract The title compounds (IV) are obtained for the first time starting from 2βmethylbenzimidazole (I) by benzoylation of the methyl group followed by cyclization of the resulting vinyl acylates (III).
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v