Features of the reaction of 3,4-dihydroxy-6-oxo-2,4-alkadienoic acid esters with acetone and p-toluidine

Autor:	Pavel A. Slepukhin, O. S. El’tsov, V. O. Koz’minykh, E. N. Koz'minykh, V. A. Andreeva, P. P. Mukovoz, I. N. Ganebnykh
Rok vydání:	2015
Předmět:	chemistry.chemical_compound 1h nmr spectroscopy Acetic acid P-toluidine chemistry 010405 organic chemistry Acetone Organic chemistry General Chemistry 010402 general chemistry 01 natural sciences 0104 chemical sciences
Zdroj:	Russian Journal of General Chemistry. 85:2715-2720
ISSN:	1608-3350 1070-3632
Popis:	Three-component reactions of 3,4-dihydroxy-6-oxo-2,4-alkadienoic acids with acetone and p-toluidine were studied; their specific feature was the formation of the regioisomeric esters of 4-hydroxy-2,2-dimethyl-1-(4-methylphenyl)-5-(2-oxoalkyliden)-2,5-dihydro-1H-pyrrole-3-carboxylic acids and [4-alkanoyl-3-hydroxy-5,5-dimethyl-1-(4-methylphenyl)-1,5-dihydro-2H-pyrrol-2-ylidene]acetic acid. Structure of the synthesized compounds was discussed based on the data of IR and 1H NMR spectroscopy and X-ray diffraction analysis.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::c36541122996e5b10a4524720c1d855f https://doi.org/10.1134/s1070363215120087 Zobrazit plný text záznamu Full text from SpringerLink