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Copper‐Catalyzed Heterocyclic Recombination of Aziridine and Diazetidine for the Synthesis of Imidazolidine.
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- Chemistry - A European Journal, 2023, v. 29, n. 43, p. 1, doi. 10.1002/chem.202301071
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- Article
Base‐catalyzed [3 + 2]/[4 + 2]‐annulations of cyclic N‐sulfimines with γ‐ and δ‐sulfonamido/hydroxy‐α,β‐unsaturated carbonyls: Stereoselective synthesis of imidazolidines, oxazolidines, hexahydropyrimidines, and 1,3‐oxazinanes
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- Bulletin of the Korean Chemical Society, 2023, v. 44, n. 7, p. 619, doi. 10.1002/bkcs.12702
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Triflamidation of Allyl-Containing Substances:Unusual Dehydrobromination vs. Intramolecular Heterocyclization.
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- Molecules, 2022, v. 27, n. 20, p. 6910, doi. 10.3390/molecules27206910
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Some Features of Phosphorylation and Benzoylation of Pyridoxal Imidazolidines.
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- Russian Journal of General Chemistry, 2021, v. 91, n. 9, p. 1667, doi. 10.1134/S1070363221090097
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Synthesis of Imidazolinium Salts by Pd/C‐Catalyzed Dehydrogenation of Imidazolidines.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 32, p. 4551, doi. 10.1002/ejoc.202100914
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Theoretical and Experimental Studies for Inhibition Potentials of Imidazolidine 4-One and Oxazolidine 5-One Derivatives for the Corrosion of Carbon Steel in Sea Water.
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- Iraqi Journal of Science, 2020, v. 61, n. 11, p. 2776, doi. 10.24996/ijs.2020.61.11.3
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[3+2] Cycloaddition of Trifluoromethylated N‐Acylhydrazones with Azomethine Ylides: Synthesis of Trifluoromethylated Imidazolidines.
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- Asian Journal of Organic Chemistry, 2020, v. 9, n. 7, p. 1036, doi. 10.1002/ajoc.202000057
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Polyhalonitrobutadienes as Versatile Building Blocks for the Biotargeted Synthesis of Substituted N-Heterocyclic Compounds †.
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- Molecules, 2020, v. 25, n. 12, p. 2863, doi. 10.3390/molecules25122863
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IMIDAZOLIDIN DERIVATIVE A NOVEL ANTI COLORECTAL CANCER AGENT.
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- Biochemical & Cellular Archives, 2020, v. 20, n. 1, p. 2051, doi. 10.35124/bca.2020.20.1.2051
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- Article
A Ring Expansion Route to Benzofused N‐Heterocycles Through Aryne Insertion into 1,3‐Diaza‐heterocycles.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 31/32, p. 5196, doi. 10.1002/ejoc.201900570
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Addition–cyclization reactions of furan-2-carbonyl isothiocyanate with nitrogen nucleophiles as a synthetic route to novel azines and azoles of potential biological activity.
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- Journal of the Iranian Chemical Society, 2019, v. 16, n. 9, p. 1853, doi. 10.1007/s13738-019-01659-6
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Pharmacophoric features for a very potent 5‐spirofluorenehydantoin inhibitor of cancer efflux pump ABCB1, based on X‐ray analysis.
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- Chemical Biology & Drug Design, 2019, v. 93, n. 5, p. 844, doi. 10.1111/cbdd.13473
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- Article
Imidazolidinone‐Tethered α‐Hydrazidopeptides – Synthesis and Conformational Investigation.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 5, p. 907, doi. 10.1002/ejoc.201801427
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Recent Advances in the Catalytic Synthesis of Imidazolidin-2-ones and Benzimidazolidin-2-ones.
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- Catalysts (2073-4344), 2019, v. 9, n. 1, p. 28, doi. 10.3390/catal9010028
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Synthesis, Characterization, and Anticancer Activity of Some Thiazole and Imidazolidine Derivatives Containing Pyridine Moiety.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 12, p. 2675, doi. 10.1134/S1070363218120320
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Access to Functionalized Imidazolidin‐2‐one Derivatives by Iron‐Catalyzed Oxyamination of Alkenes.
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- Chemistry - A European Journal, 2018, v. 24, n. 44, p. 11485, doi. 10.1002/chem.201802190
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Synthesis and Characterization of Some Heterocyclic Compounds from 1-amino-2-naphthol-4-sulfonic acid and their antibacterial activity.
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- Journals Kufa for Chamical, 2018, v. 2, n. 4, p. 57
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Identfication of Potent LXRβ-Selective Agonists without LXRα Activation by In Silico Approaches.
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- Molecules, 2018, v. 23, n. 6, p. 1349, doi. 10.3390/molecules23061349
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Preparation and Biological Activities of Some Heterocyclic Compounds Derivatives from 2-Aminothiazoles.
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- Nano Biomedicine & Engineering, 2018, v. 10, n. 2, p. 129, doi. 10.5101/nbe.v10i2.p129-140
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Design, synthesis and evaluation of anticancer activity of novel 2-thioxoimidazolidin-4-one derivatives bearing pyrazole, triazole and benzoxazole moieties.
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- Chemistry Central Journal, 2018, v. 12, n. 1, p. 1, doi. 10.1186/s13065-018-0418-1
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Crystal Structure and Catalytic Activity of A Novel Cd(II) Coordination Polymer Formed by Dicarboxylic Ligand.
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- Bulletin of Chemical Reaction Engineering & Catalysis, 2018, v. 13, n. 2, p. 220, doi. 10.9767/bcrec.13.2.1178.220-226
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SYNTHESIS OF SOME HETEROCYCLIC COMPOUNDS DERIVATIVES BY USING MELDRUM'S ACID AS STARTING MATERIAL AND STUDY OF THE BIOLOGICAL ACTIVITIES.
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- Biochemical & Cellular Archives, 2018, v. 18, n. 1, p. 789
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Three-component hetero-domino cyclization and copper-catalyzed double A<sup>3</sup>-coupling reaction of ethane-1,2-diamines, formaldehyde, and alkynes to afford 1,3-dipropargylimidazolidines.
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 3, p. 355, doi. 10.1007/s10593-018-2273-3
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Sterically Bulky NHC Adducts of GaMe<sub>3</sub> and InMe<sub>3</sub> for H<sub>2</sub> Activation and Lactide Polymerization.
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- Inorganics, 2018, v. 6, n. 1, p. 23, doi. 10.3390/inorganics6010023
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Triggered release of hexanal from an imidazolidine precursor encapsulated in poly(lactic acid) and ethylcellulose carriers.
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- Journal of Materials Science, 2018, v. 53, n. 3, p. 2221, doi. 10.1007/s10853-017-1635-z
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Synthesis and structure-activity relationships of carbohydrazides and 1,3,4-oxadiazole derivatives bearing an imidazolidine moiety against the yellow fever and dengue vector, Aedes aegypti.
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- Pest Management Science, 2018, v. 74, n. 2, p. 413, doi. 10.1002/ps.4722
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MgO Nanoparticle-Catalyzed Synthesis and Broad-Spectrum Antibacterial Activity of Imidazolidine- and Tetrahydropyrimidine-2-Thione Derivatives.
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- Applied Biochemistry & Biotechnology, 2018, v. 184, n. 1, p. 291, doi. 10.1007/s12010-017-2544-y
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Synthesis and spectrometric study of some nucleophilic reactions of the antiepileptic molecule; 5,5-diphenyl imidazolidine-2,4-dione.
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- Journal of University of Anbar for Pure Science, 2018, v. 12, n. 1, p. 38
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Synthesis of novel derivatives of (benz)imidazo[2,1-b]pyrimido[4,5-d][1,3] thiazine.
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- Journal of Chemical Research, 2017, v. 41, p. 9
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1,3-Bis(2,6-diisopropylphenyl)-2-trichloromethylimidazolidine.
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- Molbank, 2017, v. 2017, n. 4, p. m962, doi. 10.3390/M962
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Synthesis and inhibitory activity of 1,3-(adamantan-1(2)-yl)- imidazolidine-2,4,5-triones and 3,3'-(adamantan-1-yl)- bis(1-alkylimidazolidine-2,4,5-triones).
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1080, doi. 10.1007/s10593-017-2174-x
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Imidazolidine Ring Cleavage upon Complexation with First-Row Transition Metals.
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- European Journal of Inorganic Chemistry, 2017, v. 2017, n. 33, p. 3884, doi. 10.1002/ejic.201700605
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Synthesis and crystal structures of bis(imidazolidine-2-thione-κS)bis(thiocyanato-κS)mercury(II) and bis(cyanido)bis(μ<sub>2</sub>-imidazolidine-2-thione-κS)mercury(II)·Hg(CN)<sub>2</sub>.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2017, v. 77, n. 9, p. 671, doi. 10.1515/znb-2017-0080
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Synthesis of Mono-N-sulfonylimidazolidines by a 1,3-Dipolar Cycloaddition Strategy, as an Alternative to Selective NSulfonylation, and Their Ring Cleavage To Afford 1,2-Diamines.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 31, p. 4617, doi. 10.1002/ejoc.201700654
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- Article
1-[(Imidazolidin-2-yl)imino]-1 H-indoles as new hypotensive agents: synthesis and in vitro and in vivo biological studies.
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- Chemical Biology & Drug Design, 2017, v. 89, n. 3, p. 400, doi. 10.1111/cbdd.12846
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Using a Vapor-Phase Surfactant to Control Gold Metal Plate Growth.
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- Advanced Materials Interfaces, 2017, v. 4, n. 4, p. n/a, doi. 10.1002/admi.201600864
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- Article
Highly Stereoselective Synthesis of Imidazolidines through the Palladium(0)-Catalyzed Three-Component Reaction of 2,3-Allenylamines, Organic Halides, and Imines.
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- ChemCatChem, 2017, v. 9, n. 3, p. 403, doi. 10.1002/cctc.201601345
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Trapping of a Methanoato Bridge in μ-1,1,3,3 Mode for [Cu<sub>4</sub>] Aggregate Formation: Synthesis, Steric Control on Nuclearity, Antimicrobial Activity, and DNA-Interaction Properties.
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- European Journal of Inorganic Chemistry, 2017, v. 2017, n. 4, p. 769, doi. 10.1002/ejic.201601092
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2-(2-Hydroxyphenyl)imidazolidines and their O-phosphorylated derivatives.
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- Russian Journal of General Chemistry, 2017, v. 87, n. 1, p. 60, doi. 10.1134/S107036321701011X
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Synthesis of palladium complexes derived from imidazolidin-2-ylidene ligands and used for catalytic.
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- Applied Organometallic Chemistry, 2016, v. 30, n. 12, p. 1050, doi. 10.1002/aoc.3541
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Synthesis of (1,2,3-thiadiazolyl)imidazolidine-2,4-diones by microwave irradiation and characterization of their biological activity.
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- Chemistry of Heterocyclic Compounds, 2016, v. 52, n. 11, p. 910, doi. 10.1007/s10593-017-1986-z
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- Article
One-Pot Three-Component Synthesis of Vicinal Diamines via In Situ Aminal Formation and Carboamination.
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- Angewandte Chemie, 2016, v. 128, n. 41, p. 13073, doi. 10.1002/ange.201607318
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- Article
A Comprehensive Study of Copper Guanidine Quinoline Complexes: Predicting the Activity of Catalysts in ATRP with DFT.
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- Chemistry - A European Journal, 2016, v. 22, n. 38, p. 13550, doi. 10.1002/chem.201602223
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- Article
New 1,3-diaryl-5-thioxo-imidazolidin-2,4-dione derivatives: synthesis, reactions and evaluation of antibacterial and antifungal activities.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2016, v. 71, n. 8, p. 875, doi. 10.1515/znb-2016-0054
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- Article
Recyclable Enantioselective Catalysts Based on Copper(II) Complexes of 2-(Pyridine-2-yl)imidazolidine-4-thione: Their Application in Asymmetric Henry Reactions.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 15, p. 2541, doi. 10.1002/adsc.201600198
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Scientific opinion on Flavouring Group Evaluation 400 ( FGE.400): 3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1 H-pyrazol-4-yl)-1-(3-hydroxybenzyl)imidazolidine-2,4-dione.
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- EFSA Journal, 2016, v. 14, n. 7, p. n/a, doi. 10.2903/j.efsa.2016.4334
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- Article
A High Loading and Recyclable Pentaerythritol Supported Imidazolidin-4-one Catalyst for Enantioselective Diels-Alder Reactions.
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- Catalysis Letters, 2016, v. 146, n. 6, p. 1107, doi. 10.1007/s10562-016-1724-7
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Efficient Synthesis of Octacosanol Linoleate Catalyzed by Ionic Liquid and Its Structure Characterization.
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- Journal of the American Oil Chemists' Society (JAOCS), 2016, v. 93, n. 4, p. 509, doi. 10.1007/s11746-016-2793-x
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- Article
Helical Poly(phenylacetylene) Bearing Chiral and Achiral Imidazolidinone-Based Pendants that Catalyze Asymmetric Reactions due to Catalytically Active Achiral Pendants Assisted by Macromolecular Helicity.
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- Macromolecular Rapid Communications, 2015, v. 36, n. 23, p. 2047, doi. 10.1002/marc.201500456
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The Diarylprolinol Silyl Ethers: Ten Years After.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 47, p. 13860, doi. 10.1002/anie.201503920
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- Article