The tautomerism and protonation of 8-azaguanine (azaG) have been studied by means of ab initio methods, both in the gas phase and in aqueous solution. An elimination procedure to choose the most stable tautomeric forms, based on AM1 and HF/6-31G\* energies, has been applied. Tautomers azaG(1,9), aza
Theoretical description of solvent effects. X. Theoretical investigation of the Tautomerism of Nucleic Acid Bases of biological importance in the gas phase and in solution
✍ Scribed by Dr. C. Bartzsch; Doz. Dr. C. Weiss; Dr. H.-J. Hofmann
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 472 KB
- Volume
- 326
- Category
- Article
- ISSN
- 1615-4150
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Density functional calculations at the B3LYP/6‐311++G\*\* level have been performed to determine the ground‐state conformational preference for kojic acid, a widely used skin‐whitening, antibrowning, and antibacterial agent. It is found that the gas phase consists almost entirely of the
## Abstract This study was focused on distinguishing L‐ and D‐enantiomers of amino acids using electrospray ionization mass spectrometry (ESI‐MS) of ternary complexes with Cu(II) and chiral derivatives of bipyridine. A pinene‐annulated derivative of 2,2′‐bipyridine, (5__R__,7__S__,8__S__)‐(−)‐5,6,7