1990
DOI: 10.1007/bf00487424
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Synthesis of pyrrole-2-carboxylic acids and their N-vinyl derivatives

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Cited by 2 publications
(2 citation statements)
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“…The method described here offers a significant advantage, in terms of overall synthetic steps and availability of starting materials, over existing methods for the preparation of 5-arylpyrrole-2-carboxylic acids. 15,[21][22][23] Compounds 3a-j were prepared in 1-10 gram scale from a single reaction run, and no chromatographic purification was necessary.…”
Section: Table 2 Arylation Of Pyrrole With Phenyl Bromide To Form 1imentioning
confidence: 99%
“…The method described here offers a significant advantage, in terms of overall synthetic steps and availability of starting materials, over existing methods for the preparation of 5-arylpyrrole-2-carboxylic acids. 15,[21][22][23] Compounds 3a-j were prepared in 1-10 gram scale from a single reaction run, and no chromatographic purification was necessary.…”
Section: Table 2 Arylation Of Pyrrole With Phenyl Bromide To Form 1imentioning
confidence: 99%
“…Pyrrolecarboxylic acid exhibit higher biological activity. Derivatives of 5-pyrrolecarboxylic acid possess an antiviral effect, in particular, they actively suppress classical fowl plague viruses [2] and the sodium salt of 2-aryl-5-pyrrolecarboxylic acid exhibit anticonvulsant activity [3]. The aim is the creation of physical-chemical model of synthesis of methyl 5-acetyl-2-pyrrolecarboxylic acid reacting 2-acetylpyrrolyl with carbon tetrachloride and methanol under the influence of iron catalysts and carrying out its formalization, t. E. Drawing up a mathematical model, which is a system of relations reflecting the basic conservation laws (mass, energy, momentum, etc.).…”
mentioning
confidence: 99%