S. Ryng, M. Szostak
2009
Citations
0
Influential Citations
1
Citations
Journal
Polish Journal of Chemistry
Abstract
The unusual behavior of the ethyl ester of 5-amino-3-methylisoxazole-4-carboxylic acid (1) during deamination is described. Possible explanations for the anomalies of the diazotization reaction are proposed. Deamination methods leading to ethyl ester of 3-methylisoxazole-4-carboxylic acid (5) are presented. 5 will serve as a lead compound for a new series of immunomodulatory agents.