2-Hydroxy-3-aryl-6-methylpyrazines—fluorophores formed from the reaction of formaldehyde with cyclic enamine degradation products common to β-lactam antibiotics with aryl glycine side chains
- 1 September 1981
- journal article
- Published by Oxford University Press (OUP) in Journal of Pharmacy and Pharmacology
- Vol. 33 (1) , 119-121
- https://doi.org/10.1111/j.2042-7158.1981.tb13729.x
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Isolation and identification of a fluorophore from ampicillin degradationJournal of Pharmacy and Pharmacology, 1979
- Isolation and identification of the fluorescent degradation product of some β-lactam antibioticsJournal of Pharmacy and Pharmacology, 1978
- Substituent effects upon the base hydrolysis of penicillins and cephalosporins. Competitive intramolecular nucleophilic amino attack in cephalosporinsJournal of Medicinal Chemistry, 1974
- Comparative stabilities of cephalosporins in aqueous solution.The Journal of Antibiotics, 1974
- The Preparation of Hydroxypyrazines and Derived ChloropyrazinesJournal of the American Chemical Society, 1952