Margarita Likhacheva
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Margarita Likhacheva has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
- Igor V. Trushkov
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
1 shared publication - Tetyana V. Beryozkina
TOS Department, Ural Federal University, 19 Mira st., Yekaterinbug 620002, Russia
1 shared publication - Vasiliy Alekseevich Bakulev
TOS Department, Ural Federal University, 19 Mira st., Yekaterinbug 620002, Russia
1 shared publication Vera S Berseneva
TOS Department Ural Federal University 19 Mira str. 620002 Yekaterinburg Russia
1 shared publication- Vladimir G. Ilkin
TOS Department, Ural Federal University, 19 Mira st., Yekaterinbug 620002, Russia
1 shared publication - Vladimir T. Abaev
Северо-Осетинский государственный университет им. К. Л. Хетагурова
1 shared publication
Latest Publications
- Open Access
- 28 January 2026
- Published by Beilstein Institut in Beilstein Journal of Organic Chemistry
- Vol. 22, 192-204
Base-promoted deacylation of 2-acetyl-2,5-dihydrothiophenes and their oxygen-mediated hydroxylation
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.
- 28 January 2026
- Published by Beilstein Institut in Beilstein Journal of Organic Chemistry
- Vol. 22, 192-204
Open AccessBase-promoted deacylation of 2-acetyl-2,5-dihydrothiophenes and their oxygen-mediated hydroxylation
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.