Paper
Synthesis of ethyl 4-(isoxazol-4-yl)-2,4-dioxobutanoates from ethyl 5-aroyl-4-pyrone-2-carboxylates and hydroxylamine
Published Mar 1, 2017 · D. Obydennov, L. R. Khammatova, V. Sosnovskikh
Mendeleev Communications
Q3 SJR score
7
Citations
0
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
Ethyl 4-(5-arylisoxazol-4-yl)-2,4-dioxobutanoates can be synthesized from ethyl 5-aroyl-4-pyrone-2-carboxylates and hydroxylamine in ethanol at -20
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
Sign up to use Study Snapshot
Consensus is limited without an account. Create an account or sign in to get more searches and use the Study Snapshot.
Full text analysis coming soon...
References
Structure-activity relationship of pyrrolyl diketo acid derivatives as dual inhibitors of HIV-1 integrase and reverse transcriptase ribonuclease H domain.
Pyrolyl derivatives show potential as dual HIV-1 integrase and reverse transcriptase ribonuclease H inhibitors, potentially reducing drug toxic side effects and therapeutic costs.
2015·65citations·Giuliana Cuzzucoli Crucitti et al.·Journal of medicinal chemistry
Journal of medicinal chemistry
The Interaction of 2,5-Diethoxycarbonyl-and 5-Benzoyl-2-Ethoxycarbonyl-4-Pyrones with o-Phenylenediamine*
This study demonstrates a simple method for synthesizing 2,5-diethoxycarbonyl-4-pyrones and 5-benzoyl-2-ethoxycarbonyl-4-pyrones, providing potential antimicrobial and antiviral agents for medicinal chemistry.
2014·6citations·D. Obydennov et al.·Chemistry of Heterocyclic Compounds
Chemistry of Heterocyclic Compounds
Inhibiting the HIV Integration Process: Past, Present, and the Future
Inhibiting HIV integrase with new drugs and gene therapy approaches offers promising future anti-HIV treatments.
2014·44citations·R. D. Santo·Journal of Medicinal Chemistry
Journal of Medicinal Chemistry
Synthesis of 6-aryl- and 5-aroylcomanic acids from 5-aroyl-2-carbethoxy-4-pyrones via a deformylative rearrangement and ring-opening/ring-closure sequence
This study demonstrates the successful synthesis of 6-arylcomanic acids and 5-aroylcomanic acids from 5-aroyl-2-carbethoxy-4-pyrones using deformylative rearrangement and ring-opening/ring-closure sequences.
2014·13citations·D. Obydennov et al.·Tetrahedron Letters
Tetrahedron Letters
An improved synthesis and some reactions of diethyl 4-oxo-4H-pyran-2,5- dicarboxylate
Diethyl 4-oxo-4H-pyran-2,5-dicarboxylate is an efficient and efficient synthesis method for producing 4-oxo-4H-pyran-2,5-dicarboxylic and 4-oxo-1-phenyl-1,4-dihydropyridine
2013·17citations·D. Obydennov et al.·Tetrahedron Letters
Tetrahedron Letters
Carbamoyl pyridone HIV-1 integrase inhibitors 3. A diastereomeric approach to chiral nonracemic tricyclic ring systems and the discovery of dolutegravir (S/GSK1349572) and (S/GSK1265744).
Dolutegravir and S/GSK1265744 are potential once-daily HIV-1 integrase inhibitors with superior potency against resistant viral strains, and their discovery was achieved through a diastereoselective synthetic strategy.
2013·159citations·B. Johns et al.·Journal of medicinal chemistry
Journal of medicinal chemistry
A novel, two-step synthesis of 4-pyridone-3-carboxamides from 2-cyano-4-pyrones
This study presents a novel two-step synthesis of 4-pyridone-3-carboxamides from 2-cyano-4-pyrones, achieving high yields of 31-70% in the first step and 31-70% in the second step.
2013·15citations·D. Obydennov et al.·Tetrahedron Letters
Tetrahedron Letters
Preparation and rearrangement of N-vinyl nitrones: synthesis of spiroisoxazolines and fluorene-tethered isoxazoles.
N-vinyl nitrones derived from fluorenone can be prepared and rearranged to produce spiroisoxazolines and fluorene-tethered isoxazoles, with potential applications in organic synthesis.
2012·61citations·Dong‐Liang Mo et al.·Organic letters
Organic letters
Reactions of 6-(tri- and 6-(difluoromethyl))comanic acids and their ethyl esters with aniline and its 2-substituted derivatives
6-(tri- and 6-(difluoromethyl))comanic acids can synthesize R-containing derivatives of 4-pyridones, benzodiazepines, and quinoxalinones, with potential applications in organic synthesis.
2012·12citations·D. Obydennov et al.·Journal of Fluorine Chemistry
Journal of Fluorine Chemistry
Citations
2,4-Diketo esters: Crucial intermediates for drug discovery.
2,4-diketo esters are crucial intermediates in drug discovery due to their versatile synthesis and potential clinical applications in various diseases.
2020·30citations·Nenad Joksimović et al.·Bioorganic chemistry
Bioorganic chemistry
Synthesis of novel polycarbonyl Schiff bases by ring-opening reaction of ethyl 5-acyl-4-pyrone-2-carboxylates with primary mono- and diamines
This study developed a novel method for synthesizing novel polycarbonyl Schiff bases with high yields and selectivity, enabling the design of salphen structures and other complex ligands.
2019·5citations·D. Obydennov et al.·RSC Advances
RSC Advances
Nitrosylsulfuric acid in the synthesis of 5-chloroisoxazoles from 1,1-dichlorocyclopropanes
Nitrosylsulfuric acid is a useful reagent for synthesizing 5-chloroisoxazoles from 1,1-di-chlorocyclopropanes, with some showing cytotoxicity against various cell lines.
2019·2citations·O. B. Bondarenko et al.·Mendeleev Communications
Mendeleev Communications
Reactions of carbamoylated amino enones with 3-substituted chromones for the preparation of 2-pyridones and chromeno[4,3-b]pyridine-2,5-diones
Carbamoylated amino enones react regioselectively with 3-substituted chromones to form 2-pyridones and chromeno[4,3-b]pyridine-2,5-diones bearing the amino enone moiety.
2019·5citations·D. Obydennov et al.·Mendeleev Communications
Mendeleev Communications
A chemo- and regiocontrolled approach to bipyrazoles and pyridones via the reaction of ethyl 5-acyl-4-pyrone-2-carboxylates with hydrazines.
This study presents a novel chemo- and regiocontrolled approach to synthesize bipyrazoles and pyridones using ethyl 5-acylcomanoates with hydrazines, enabling the easy switching of pyrazole ring structures and pyridone
2018·11citations·D. Obydennov et al.·Organic & biomolecular chemistry
Organic & biomolecular chemistry