## Abstract Indomethacine (**1**) and acemethacine (**2**) contain the substituents ‐OCH~3~, ‐CH~2~COOH, ‐CH~2~COOCH~2~COOH, C‐indole and O‐benzoyl, which are susceptible to protonation in highly acidic media. To determine the protonation sites and the substituent effects reliably, the dissociation
Protonation of kanamycin A: Detailing of thermodynamics and protonation sites assignment
✍ Scribed by Yanet Fuentes-Martínez; Carolina Godoy-Alcántar; Felipe Medrano; Alexander Dikiy; Anatoly K. Yatsimirsky
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 413 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0045-2068
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