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Natalia Sucman
Natalia Sucman
Moldova State University, Institute of Chemistry
Подтвержден адрес электронной почты в домене ichem.md
Название
Процитировано
Процитировано
Год
Highly Enantio‐and Diastereoselective Generation of Two Quaternary Centers in Spirocyclopropanation of Oxindole Derivatives.
A Noole, NS Sucman, MA Kabeshov, T Kanger, FZ Macaev, AV Malkov
Chemistry–A European Journal 18 (47), 14929-14933, 2012
902012
Text reading in English as a second language: Evidence from the Multilingual Eye-Movements Corpus
V Kuperman, N Siegelman, S Schroeder, C Acartürk, S Alexeeva, ...
Studies in Second Language Acquisition 45 (1), 3-37, 2023
482023
Facile and Convenient One-Pot Process for the Synthesis of Spirooxindole Derivatives in High Optical Purity Using (−)-(S)-Brevicolline as an Organocatalyst
F Macaev, N Sucman, F Shepeli, M Zveaghintseva, V Pogrebnoi
Symmetry 3 (2), 165-170, 2011
332011
Recent advances in the use of cyclodextrins in antifungal formulations
F Macaev, V Boldescu, A Geronikaki, N Sucman
Current topics in medicinal chemistry 13 (21), 2677-2683, 2013
292013
Synthesis and antiviral activity of new thiazole, 1, 2, 4-triazol and oxindole derivatives
O Radul, N Sucman, S Pogrebnoi, A Barbă, F Macaev
Chemistry Journal of Moldova 6 (1), 101-109, 2011
232011
Synthesis and structure of new oxoindoles
FZ Macaev, OM Radul, IN Shterbet, SI Pogrebnoi, NS Sucman, ...
Chemistry of Heterocyclic Compounds 43, 298-305, 2007
172007
Selective transformations of isatins to substituted 2-oxindoles
FZ Macaev, NS Sucman, VV Boldescu
Russian Chemical Bulletin 63, 15-25, 2014
162014
Initial Synthesis of Diastereomeric Pyran Spirooxoindolinones Based on (–)-Carvone and (+)-3-Carene
FZ Macaev, NS Sucman, SI Pogrebnoi, LP Logina, AN Barba
Chemistry of natural compounds 50, 103-108, 2014
152014
Enantioselective Vinylogous Reactions of 3-Alkylidene Oxindoles
R Dalpozzo, R Mancuso
Synthesis 50 (13), 2463-2472, 2018
142018
Recent application of isatins in synthesis of functionalized spirocyclic oxindoles
F Macaev, N Sucman, A Geronikaki
Targets in Heterocyclic Systems 15, 294-326, 2011
142011
The synthesis of new spirolactones from substituted isatins
N Sucman, V Pogrebnoi, M Obushak, E Melnik, V Kravtsov, F Makaev
Chemistry Journal of Moldova 10 (1), 64-70, 2015
52015
Molecular concepts of macrophage targeting
V Boldescu, V Krudu, N Sucman, S Pogrebnoi, M Zveaghintseva, ...
Chemistry Journal of Moldova 8 (2), 21-31, 2013
52013
Ionic liquids derivative of 1н-imidazole as novel reagents, catalysts and solvents
MV Şargarovschi, N Sucman, T Iudin, D Duca, E Styngach, D Prodius, ...
Chemistry Journal of Moldova 5 (1), 36-56, 2010
52010
Ionic liquids derivative of 1н-imidazole as novel reagents, catalysts and solvents
MV Şargarovschi, N Sucman, T Iudin, D Duca, E Styngach, D Prodius, ...
Chemistry Journal of Moldova 5 (1), 36-56, 2010
52010
Ectonucleotidase Inhibitory and Redox Activity of Imidazole‐Based Organic Salts and Ionic Liquids
V Boldescu, N Sucman, S Hassan, J Iqbal, M Neamtu, J Lecka, J Sévigny, ...
ChemMedChem 13 (21), 2297-2304, 2018
42018
Synthesis of New 5-Aryl-1, 3, 4-Oxadiazol-Thioureas and Oxadiazol-Thioxopyrimidinones Derivatives of Monoterpenes and Evaluation of their Catalytic Efficiency for Strecker-type …
FZ Macaev, Z Ribkovskaia, L Bets, N Sucman, S Pogrebnoi
The All Results Journals: Chem 3 (2), 12-18, 2012
42012
Molecular diversity from nitrogen organic salts: preparation of novel scaffolds and focused targets
S Curlat, N Sucman, E Styngach, S Pogrebnoi, V Boldescu, V Stefanet, ...
Materials Science and Condensed Matter Physics, 94-94, 2018
32018
Amides of Dehydroabietic Acid Based on 5-Aminooxoindoles and Their Transformation Products
VS Pogrebnoi, SI Pogrebnoi, EP Stingaci, NS Sucman, FZ Macaev
Chemistry of Natural Compounds 58 (5), 874-881, 2022
22022
Synthesis of (–)-Convolutamydine a Derivatives and Analogs
DY Bilan, NS Sucman, OM Radul, IP Dragalin, AN Barba, FZ Macaev
Chemistry of Natural Compounds 57 (3), 516-520, 2021
12021
Sinteza derivaților de amino acizi ai 2-hidroxijuglonei cu dezvoltarea potențială a activității biologice
T Andrusenco, N Sucman, V Boldescu, V Valica, L Uncu, F Macaev
Farmacia secolului XXI–Între specializarea inteligentă și responsabilitatea …, 2018
12018
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