Synthesis and structure of new substituted furan-3-carboxylate hydrazones

The reaction of acetyl-containing furan-3-carboxylates with substituted hydrazines in an alcohol solution leads to the formation of substituted furan-3-carboxylate hydrazones. The resulting hydrazones have E -configuration, as determined by NMR spectroscopy and X-ray diffraction analysis.

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Bibliographic Details
Published in:	Chemistry of heterocyclic compounds (New York, N.Y. 1965) Vol. 60; no. 3-4; pp. 133 - 137
Main Authors:	Gomonov, Kirill A., Pelipko, Vasilii V., Litvinov, Igor A., Baichurin, Ruslan I., Makarenko, Sergey V.
Format:	Journal Article
Language:	English
Published:	New York Springer US 01-04-2024 Springer Nature B.V
Subjects:	Carboxylates Chemical synthesis Chemistry Chemistry and Materials Science Hydrazines Hydrazones NMR spectroscopy Organic Chemistry Pharmacy Substitutes molecular structure NOE effect hydrazines isomers furancarboxylates hydrazones X-ray diffraction analysis
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Description
Summary:	The reaction of acetyl-containing furan-3-carboxylates with substituted hydrazines in an alcohol solution leads to the formation of substituted furan-3-carboxylate hydrazones. The resulting hydrazones have E -configuration, as determined by NMR spectroscopy and X-ray diffraction analysis.
ISSN:	0009-3122 1573-8353
DOI:	10.1007/s10593-024-03308-0