The Tautomeric Forms of Cyameluric Acid Derivatives
✍ Scribed by Nadia E. A. El-Gamel; Lena Seyfarth; Jörg Wagler; Helmut Ehrenberg; Marcus Schwarz; Jürgen Senker; Edwin Kroke
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 555 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0947-6539
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📜 SIMILAR VOLUMES
In order to identify the structure of the most stable tautomers of 6-amino-5-nitrosouracil and violuric acid derivatives in different pH conditions, relative stabilities of potential tautomers (112) in aqueous phase have been calculated taking into account the entropy effects over the tautomeric equ
Ill 301 (3,0); 284 (4,0); 220 (3,0); 209 (100,0); 199 (1,5); 165 (2,0); 130 (13,0); ll8 (3,0); Ill (7,0); 104 (22,0); 89 (5,0) IV 381 (3,6); 209 (100,0); 196 (2,0); 191 (7,0); 182 (6,0); 171 (5,0); 166 (7,0); 155 (15,0); 130 (59,0); 102 (41,0); 89 (23,5) V 315 (10,0); 298 (30,0); 224 (6,0); 209 (28,