Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/123456789/33012
Title: Base-promoted deacylation of 2-acetyl-2,5-dihydrothiophenes and their oxygen-mediated hydroxylation
Authors: Abaev, V. T.
Абаев, В. Т.
Keywords: 2-acetyl-2,5-dihydrothiophenes;2-hydroxy-2,5-dihydrothiophenes;Deacylation;Transformations
Issue Date: 2026
Publisher: Beilstein-Institut Zur Forderung der Chemischen Wissenschaften
Citation: Ilkin V. G., Likhacheva M., Trushkov I. V., Beryozkina T. V., Berseneva V. S., Abaev V. T., Dehaen W., Bakulev V. A. Base-promoted deacylation of 2-acetyl-2,5-dihydrothiophenes and their oxygen-mediated hydroxylation // Beilstein Journal of Organic Chemistry. - 2026. - 22 (1). - pp. 192 - 204. - DOI: 10.3762/BJOC.22.13
Series/Report no.: Beilstein Journal of Organic Chemistry
Abstract: Solvent-dependent transformations of polysubstituted 2-acetyl-2,5-dihydrothiophenes to the corresponding 2-hydroxy- or deacetylated derivatives are described. The treatment of a methanolic solution of the dihydrothiophene substrates with sodium methoxide afforded the deacylated products. Conversely, the treatment with sodium ethoxide in an oxygen saturated ethanolic solution produced 2-hydroxy substituted 2,5-dihydrothiophenes.
URI: https://dspace.ncfu.ru/handle/123456789/33012
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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