- PII
- 10.31857/S0044460X23030071-1
- DOI
- 10.31857/S0044460X23030071
- Publication type
- Article
- Status
- Published
- Authors
- Volume/ Edition
- Volume 93 / Issue number 3
- Pages
- 385-392
- Abstract
- The reactions of 5,5-dialkyl- N -alkyl-2-imino-2,5-dihydrofuran-3-carboxamide thiosemicarbazones with diethyl acetylenedicarboxylate and maleic anhydride in absolute ethanol gave rise to potentially bioactive compounds containing iminodihydrofuran and 4-oxothiazolidine rings. The synthesized compounds were characterized by 1H and 13C NMR spectroscopy and elemental analysis data.
- Keywords
- диэтилацетилендикарбоксилат малеиновый ангидрид тиосемикарбазоны иминодигидрофуранов 4-oксотиазолидин
- Date of publication
- 16.09.2025
- Year of publication
- 2025
- Number of purchasers
- 0
- Views
- 14
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