Alkylation of Imidazole-4(5)-carboxylic Acid Derivatives with Methyl Bromoacetate
β Scribed by M. A. Dumpis; E. M. Alekseeva; E. V. Litasova; L. B. Piotrovskii
- Book ID
- 110437344
- Publisher
- Springer
- Year
- 2003
- Tongue
- English
- Weight
- 48 KB
- Volume
- 73
- Category
- Article
- ISSN
- 1070-3632
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π SIMILAR VOLUMES
The hydrolysis of ethyl 1-methyl-4-nitro-1H-imidazole-2carboxylate leads to 1-methyl-4-nitro-1H-imidazol-2carboxylic acid, which crystallizes as a dihydrate, C 5 H 5 N 3 O 4 Γ2H 2 O. The planar organic entity is a flat molecule; the molecules are linked through the water molecules by hydrogen bondin
## Abstract 1βArylalkylβ5βphenylsulfonaminoβimidazoleβ4βcarboxylic acid esters and their carboxamides with an additional secondary amino group were synthesized and identified as antiplatelet agents in a low micromolar range (Bornβtest, inducer collagen). To describe the mechanism of action more pre