Thioamides of 5-nitrofuran-2-carboxylic and 3-(5′-nitrofuryl-2′) acrylic acids
✍ Scribed by B. V. Kurgan; S. A. Hiller
- Book ID
- 112393396
- Publisher
- Springer US
- Year
- 1967
- Tongue
- English
- Weight
- 237 KB
- Volume
- 2
- Category
- Article
- ISSN
- 0009-3122
No coin nor oath required. For personal study only.
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## Abstract Monitoring the enforcement of an EU-wide ban of nitrofuran antibiotics in the food production chain is a challenging task, given the nature of nitrofuran compounds. The original and modified Fenton reactions are advanced oxidation processes that can eliminate the toxicity of nitrofurans
## Abstract magnified image Reduction of the Michael addition products of anions of nitro compounds to dimethyl maleate led to the spontaneous formation of the respective 2‐alkyl‐5‐oxopyrrolidine‐3‐carboxylic acid methyl esters. Conventional hydrolysis of the later gave the desired compounds.