Ring-chain tautomerism in the products of the reaction between 5-substituted furfurylamines and anhydrides of α,β-unsaturated carboxylic acids

The reactions of 5-substituted furfurylamines with anhydrides of α,β-unsaturated carboxylic acids (acryloyl chloride and maleic anhydride) were studied. The first step of the reaction mechanism involved acylation of furfurylamine nitrogen atom, followed by a stereospecific, spontaneous intramolecula...

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Veröffentlicht in:	Chemistry of heterocyclic compounds (New York, N.Y. 1965) N.Y. 1965), 2016-04, Vol.52 (4), p.225-236
Hauptverfasser:	Zubkov, Fedor I., Golubev, Victor D., Zaytsev, Vladimir P., Bakhanovich, Olga V., Nikitina, Evgeniya V., Khrustalev, Victor N., Aysin, Rinat R., Timofeeva, Tatiana V., Novikov, Roman A., Varlamov, Aleksey V.
Format:	Artikel
Sprache:	eng
Schlagworte:	Acrylic acid Acylation Amides Chemistry Chemistry and Materials Science Diels-Alder reaction Maleic anhydride Nitrogen Nuclear magnetic resonance spectroscopy Organic acids Organic Chemistry Pharmacy Thiophene
Online-Zugang:	Volltext
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