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Structure-Activity Study on Anticonvulsant (Thio) Hydantoins Using Molecular Connectivity Indices
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Model for Prediction of Anti‐HIV Activity of 2‐Pyridinone Derivatives Using Novel Topological Descriptor
inferred← citeshttps://doi.org/10.1002/qua.24017openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10593-019-02507-4openalex-snapshot
Synthesis of 3-adamantylated hydantoins and their 2-thio(seleno) analogs
inferred← citeshttps://doi.org/10.1007/s11094-014-1012-zopenalex-snapshot
Assessment of Quantitative Structure-Anticonvulsive Activity Relationships in a Series of Derivatives of 1,2,3-Triazole(1H), 1,2,4-Triazole(4H), 1,3,4-Oxadiazole(1H), and 1,3,4-Thiadiazole(1H)
inferred← citeshttps://doi.org/10.1016/j.bmc.2005.02.033openalex-snapshot
Topological models for prediction of anti-HIV activity of acylthiocarbamates
inferred← citeshttps://doi.org/10.1016/j.molstruc.2008.04.053openalex-snapshot
Synthesis and characterization of copper(II) and nickel(II) complexes of (9′-fluorene)-spiro-5-dithiohydantoin
inferred← citeshttps://doi.org/10.1016/j.molstruc.2013.07.044openalex-snapshot
Mercury(II) complexes with 5-methyl-5-(4-pyridyl)-2,4-imidazolidenedione: Synthesis, structural characterization, and theoretical studies
inferred← citeshttps://doi.org/10.1016/j.saa.2014.08.002openalex-snapshot
Pd(II) and Pd(IV) complexes with 5-methyl-5-(4-pyridyl)hydantoin: Synthesis, physicochemical, theoretical, and pharmacological investigation
inferred← citeshttps://doi.org/10.1016/j.tet.2005.12.037openalex-snapshot
An eco-friendly protocol for synthesis of thiourea derivatives: 1-benzoyl-3-benzylguanidine and 1-benzoyl-3-benzyl-O-ethylisourea. A possible non-purely thermal microwave assisted reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153983openalex-snapshot
One-pot high-throughput synthesis of N3-substituted 5-arylidene-2-thiohydantoin amides and acids
inferred← citeshttps://doi.org/10.1021/ci025639wopenalex-snapshot
Development of Quantitative Structure−Activity Relationships and Classification Models for Anticonvulsant Activity of Hydantoin Analogues
inferred← citeshttps://doi.org/10.1021/jm9507035openalex-snapshot
Evolutionary Optimization in Quantitative Structure−Activity Relationship: An Application of Genetic Neural Networks
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Powerful Approach to Heterocyclic Skeletal Diversity by Sequential Three-Component Reaction of Amines, Isothiocyanates, and 1,2-Diaza-1,3-dienes
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Synthesis, X-ray crystallography and antimicrobial activity of 2-cyanoguanidinophenytoin
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Integrated DFT, molecular docking, and molecular dynamics investigation of some novel 2-thiohydantoin analogues as potent CDK2 inhibitors for anticancer therapy
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Hydrogen bonded dimers vs. one-dimensional chains in 2-thiooxoimidazolidin-4-one (thiohydantoin) drug derivatives
inferred← citeshttps://doi.org/10.1039/c2ra22487aopenalex-snapshot
Thermal fragmentation of spirodithiohydantoins: A novel route to NHCs
inferred← citeshttps://doi.org/10.1039/c3cc41254gopenalex-snapshot
Synthesis of substituted hydantoins in low melting mixtures
inferred← citeshttps://doi.org/10.1080/00397911.2015.1052506openalex-snapshot
Simple and Efficient Synthesis of 5-Substituted-3-phenyl-2-thioxoimidazolidin-4-one Derivatives fromS-Amino Acids and Phenylisothiocyanate in Et3N/DMF-H2O
inferred← citeshttps://doi.org/10.1081/scc-200054778openalex-snapshot
Microwave‐Assisted Solid‐State Synthesis and Characterization of Thiohydantoin Derivatives
inferred← citeshttps://doi.org/10.1590/1808-1657v67n1p1252000openalex-snapshot
CONTRIBUIÇÃO À QUÍMICA DAS IMIDAZOLIDINADIONAS - SÍNTESE DE CICLANILIDENO-HIDANTOÍNAS
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(Z)-2′-((Adamantan-1-yl)thio)-1,1′-dimethyl-2′,3′-dihydro-[2,4′-biimidazolylidene]-4,5,5′(1H,1′H,3H)-trione
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Theoretical density functional study of gas-phase tautomerization and acidity of 5-methylhydantoin and its thio derivatives
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