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National Institutes of Health
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Ugi reactions with ammonia offer rapid access to a wide range of 5-aminothiazole and oxazole derivatives.
The Journal of organic chemistry
Corpus ID: 22029226
A series of Ugi reactions has been successfully performed using ammonia as the amine component, employing 2,2,2-trifluoroethanol…
In vivo biological activity of antioxidative aminothiazole derivatives.
Chemical & pharmaceutical bulletin
Corpus ID: 1055777
For the development of novel antioxidants having therapeutic utility, a new series of condensed 4- and 5-aminothiazole…
Evaluation of the Inhibitory Activity on Serine and Aspartic Proteases of 4‐Amino‐4H‐1,2,4‐triazole and 5‐Aminothiazole Derivatives Structurally Related to β‐Lactam Antibiotics
The Journal of pharmacy and pharmacology
Corpus ID: 29344894
Abstract— Twenty new derivatives of 4‐amino‐4H‐1,2,4‐triazole and 5‐aminothiazole have been examined for their inhibitory…
4-Amino-4H-1,2,4-triazole and 5-aminothiazole derivatives structurally related to β-lactam antibiotics as potential inhibitors of serine proteases
Corpus ID: 82372329
Synthesis and biological evaluation of 5-aminothiazole and 4-amino-1,2,4-triazole derivatives, potential inhibitors of bacterial serine enzymes
Corpus ID: 84057615
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