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Thioureas
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inferred← citeshttps://doi.org/10.2139/ssrn.4866242openalex-extracted
Synthesis and Chemical Recycling Investigations of Polythioureas
inferred← citeshttps://doi.org/10.2139/ssrn.4877570openalex-extracted
Synthesis and Chemical Recycling Investigations of Polythioureas
inferred← citeshttps://doi.org/10.1002/(sici)1096-9063(199802)52:2<145::aid-ps677>3.0.co;2-jopenalex-snapshot
Antifungal activity of 1,3-disubstituted symmetrical and unsymmetrical thioureas
inferred← citeshttps://doi.org/10.1002/14356007.a26_803openalex-snapshot
Thiourea and Thiourea Derivatives
inferred← citeshttps://doi.org/10.1002/14356007.a26_803.pub2openalex-snapshot
Thiourea and Thiourea Derivatives
inferred← citeshttps://doi.org/10.1002/14356007.a26_803.pub3openalex-snapshot
Thiourea and Thiourea Derivatives
inferred← citeshttps://doi.org/10.1002/1521-3765(20011015)7:20<4477::aid-chem4477>3.0.co;2-iopenalex-snapshot
C−H Activation with Elemental Sulfur: Synthesis of Cyclic Thioureas from Formaldehyde Aminals and S8
inferred← citeshttps://doi.org/10.1002/9780470771099.ch15openalex-snapshot
Thiolo, thiono and dithio acids and esters
inferred← citeshttps://doi.org/10.1002/ajoc.201600385openalex-snapshot
S8‐Mediated One‐Pot Synthesis of Thioamides from Benzyl Chlorides and Amines
inferred← citeshttps://doi.org/10.1002/ange.19550671602openalex-snapshot
Thioharnstoff‐Derivate als Rodentizide und ihr Nachweis bei Tiervergiftungen
inferred← citeshttps://doi.org/10.1002/aoc.4342openalex-snapshot
Design and synthesis of novel thiourea metal complexes with controllable antibacterial properties
inferred← citeshttps://doi.org/10.1002/aoc.6709openalex-snapshot
Europhtal: An industrial cobalt phthalocyanine complex as the efficient catalyst for synthesis of thioamides by one‐pot reaction of mercaptans and amines
inferred← citeshttps://doi.org/10.1002/bscb.19710800520openalex-snapshot
Study of the Kinetics, Intermediates and Product Distribution in the Synthesis and Decomposition Reactions of Thiourea Derivatives
inferred← citeshttps://doi.org/10.1002/cber.19560890707openalex-snapshot
Die Umsetzung von Benzilsäure mit Thioharnstoff
inferred← citeshttps://doi.org/10.1002/chem.202303703openalex-snapshot
Sulfur‐ and Amine‐ Promoted Multielectron Autoredox Transformation of Nitromethane: Multicomponent Access to Thiourea Derivatives
inferred← citeshttps://doi.org/10.1002/chir.22794openalex-snapshot
High‐performance liquid chromatographic enantioseparation of N‐aryl‐thioureidoalkylphosphonates and thiourylenedi(alkylphosphonates) on polysaccharide‐based chiral stationary phases
inferred← citeshttps://doi.org/10.1002/cjoc.200790095openalex-snapshot
Preparation, Crystal Structure and Theoretical Calculation ofN‐(Pyrimidin‐2‐yl)‐N′‐methoxycarbonyl‐thiourea
inferred← citeshttps://doi.org/10.1002/cjoc.200990097openalex-snapshot
Synthesis and Antiviral Activities of Chiral Thiourea Derivatives
inferred← citeshttps://doi.org/10.1002/jat.3464openalex-snapshot
A review on acridinylthioureas and its derivatives: biological and cytotoxic activity
inferred← citeshttps://doi.org/10.1002/jbt.70904openalex-snapshot
Design of Novel Hybrid Thiourea–Phosphonate Derivatives as Potential Anti‐TMV Agents: In Silico Evaluation and (S,O)‐Pharmacophoric Site Identification
inferred← citeshttps://doi.org/10.1002/jccs.197500012openalex-snapshot
Solvent and Substituent Effects on the Spectra of Some Substituted Thioureas
inferred← citeshttps://doi.org/10.1002/jccs.200100034openalex-snapshot
The Synthesis of N‐(Glycosylthioureylene)‐aminothiophosphonic and ‐diaminothiophosphinic O‐aryl Esters
inferred← citeshttps://doi.org/10.1002/jps.2600511103openalex-snapshot
Substituted Heterocyclic Thioureas I
inferred← citeshttps://doi.org/10.1002/pc.25510openalex-snapshot
Development of cashew nut shell carbon reinforced thiourea based biophenolic benzoxazine‐epoxy composites: High performance biobased coating materials
inferred← citeshttps://doi.org/10.1002/pol.1965.100030820openalex-snapshot
Effect of thiourea on the radical polymerization of vinyl monomers. Part I. Polymerization of acrylonitrile with the hydrogen peroxide–thiourea catalyst system
inferred← citeshttps://doi.org/10.1002/prac.19620160314openalex-snapshot
Umsetzungsprodukte von chlorierten Benzyl‐chloriden und ihre Verwendbarkeit als Schädlingsbekämpfungsmittel
inferred← citeshttps://doi.org/10.1002/prac.19873290210openalex-snapshot
Zur Kupplung von 4‐substituierten 2‐Pyrazolin‐5‐onen mit p‐Chinondiiminkationen; Nachweis isokinetischer Beziehungen
inferred← citeshttps://doi.org/10.1002/recl.19690880804openalex-snapshot
Reaction between chlorodiphenylacetic acid and thiourea
inferred← citeshttps://doi.org/10.1002/slct.202101635openalex-snapshot
Sulfamic Acid as Versatile Green Catalyst Used For Synthetic Organic Chemistry: A Comprehensive Update
inferred← citeshttps://doi.org/10.1002/zaac.19774330131openalex-snapshot
Borverbindungen. 6. Darstellung und Molekülstruktur des 1,5‐Diäthyl‐2,3‐diphenyl‐1,3,5‐triaza‐2‐bora‐cyclooctan‐4‐ons: Vergleichsverbindungen
inferred← citeshttps://doi.org/10.1007/1-4020-3689-2_15openalex-snapshot
Low Molecular-Mass Organic Gelators
inferred← citeshttps://doi.org/10.1007/978-3-642-03692-7_4openalex-snapshot
Synthesis and Antiviral Activity of Chiral Thiourea Derivatives
inferred← citeshttps://doi.org/10.1007/b136352openalex-snapshot
Chiral Ureas and Thiroureas in Asymmetric Catalysis
inferred← citeshttps://doi.org/10.1007/bf00471148openalex-snapshot
Synthesis of substituted thiazoles and oxazoles from 2-amino-1-(p-nitrophenyl)ethanol
inferred← citeshttps://doi.org/10.1007/bf00471632openalex-snapshot
Biologically active heterocyclic analogs of thiourea (review)
inferred← citeshttps://doi.org/10.1007/bf00764458openalex-snapshot
Synthesis and immunomodulating activity of N-(2-vinyloxyethyl)thioureas
inferred← citeshttps://doi.org/10.1007/bf02162528openalex-snapshot
Activité tuberculostatique de thiouréesortho- etméta-substituées
inferred← citeshttps://doi.org/10.1007/bf02857819openalex-snapshot
Synthesis and anti-inflammatory and analgesic activities of 2,4-di-n-butyl-3,5-diarylimino-1,2,4-thiadiazolidines
inferred← citeshttps://doi.org/10.1007/bf02980450openalex-snapshot
Synthesis and anti inflammatory and analgesic activities of 2,4-diethyl-3,5-diarylimino-1,2,4-thiadiazolidines
inferred← citeshttps://doi.org/10.1007/s00044-013-0883-yopenalex-snapshot
Synthesis, characterization, and antibacterial activities of some novel N,N′-disubstituted thiourea, 2-amino thiazole, and imidazole-2-thione derivatives
inferred← citeshttps://doi.org/10.1007/s00044-017-1829-6openalex-snapshot
Synthesis, computational studies and biological evaluation of new 1-acetyl-3-aryl thiourea derivatives as potent cholinesterase inhibitors
inferred← citeshttps://doi.org/10.1007/s00706-011-0583-6openalex-snapshot
Microwave-assisted synthesis of symmetrical and unsymmetrical N,N′-disubstituted thioureas and ureas over MgO in dry media
inferred← citeshttps://doi.org/10.1007/s00706-015-1465-0openalex-snapshot
A mild one-pot synthesis of S-aryl carbamimidothioates using diazonium salts under catalyst-free condition
inferred← citeshttps://doi.org/10.1007/s00706-017-2013-xopenalex-snapshot
Rapid and efficient protocol for Willgerodt–Kindler’s thioacetamides catalyzed by sulfated polyborate
inferred← citeshttps://doi.org/10.1007/s00706-022-02991-zopenalex-snapshot
A novel synthesis of functionalized sulfonamide derivatives using the reaction of substituted thiourea or oxime derivatives with N-(2,3-dibromopropyl)-aryl(alkyl)sulfonamides
inferred← citeshttps://doi.org/10.1007/s10311-012-0394-yopenalex-snapshot
Green synthesis of symmetrical N, N′-disubstituted thiourea derivatives in water using solar energy
inferred← citeshttps://doi.org/10.1007/s10870-008-9482-zopenalex-snapshot
Synthesis and Crystal Structure Analysis of Thiourea-Pendant Pyridines
inferred← citeshttps://doi.org/10.1007/s11030-010-9298-6openalex-snapshot
Highly efficient and catalyst-free synthesis of substituted thioureas in water
inferred← citeshttps://doi.org/10.1007/s11164-013-1100-9openalex-snapshot
Synthesis, characterization and properties of 3,3′-diethyl-1,1′-oxydiethylenedicarbonyl bis(thiourea)
inferred← citeshttps://doi.org/10.1007/s11426-010-4179-5openalex-snapshot
Synthesis and antiviral bioactivities of novel chiral bis-thiourea-type derivatives containing α-aminophosphonate moiety
inferred← citeshttps://doi.org/10.1007/s11696-017-0273-xopenalex-snapshot
Domino synthesis of quinazolin-4-yl thioureido alkanoates
inferred← citeshttps://doi.org/10.1007/s13738-023-02946-zopenalex-snapshot
A novel catalyst-free method for the synthesis of mono-N-substituted thioureas in water
inferred← citeshttps://doi.org/10.1007/s41061-017-0169-9openalex-snapshot
Sulfur-Containing Agrochemicals
inferred← citeshttps://doi.org/10.1016/0015-6264(71)90085-xopenalex-snapshot
Comparative effects of 60-day feeding of maneb and of ethylenethiourea on thyroid electrophoretic patterns of rats
inferred← citeshttps://doi.org/10.1016/0045-6535(86)90532-1openalex-snapshot
Experimental determination and prediction of partition coefficients of thioureas and their toxicity to
inferred← citeshttps://doi.org/10.1016/b0-08-044705-8/00197-7openalex-snapshot
Functions With at Least One Chalcogen Other Than Oxygen
inferred← citeshttps://doi.org/10.1016/b0-08-044705-8/00228-4openalex-snapshot
Functions Containing a Thiocarbonyl Group Bearing Two Heteroatoms Other Than a Halogen or Chalcogen
inferred← citeshttps://doi.org/10.1016/b0-08-044705-8/09014-2openalex-snapshot
References to Volume 6
inferred← citeshttps://doi.org/10.1016/b978-0-08-052349-1.00163-3openalex-snapshot
Synthesis of Thioamides and Thiolactams
inferred← citeshttps://doi.org/10.1016/j.apcata.2012.03.012openalex-snapshot
Sulfated tungstate: An efficient catalyst for synthesis of thioamides via Kindler reaction
inferred← citeshttps://doi.org/10.1016/j.bioorg.2015.08.001openalex-snapshot
Synthesis, biological evaluation, and docking studies of novel thiourea derivatives of bisindolylmethane as carbonic anhydrase II inhibitor
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.02.011openalex-snapshot
Investigation on the effect of alkyl chain linked mono-thioureas as Jack bean urease inhibitors, SAR, pharmacokinetics ADMET parameters and molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.102941openalex-snapshot
Evaluation of thioamides, thiolactams and thioureas as hydrogen sulfide (H2S) donors for lowering blood pressure
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105017openalex-snapshot
A review on diverse heterocyclic compounds as the privileged scaffolds in non-steroidal aromatase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.108719openalex-snapshot
Design, synthesis, and antimicrobial activity of new thiourea-uracil derivatives: Anti-biofilm, ROS, DHFR, computational and SAR studies
inferred← citeshttps://doi.org/10.1016/j.bmc.2010.03.033openalex-snapshot
Silica-supported fluoroboric acid (HBF4–SiO2) catalyzed highly productive synthesis of thiomorpholides as activators of l-asparaginase as well as the antioxidant agent
inferred← citeshttps://doi.org/10.1016/j.bmcl.2015.11.058openalex-snapshot
Synthesis, antibacterial and anti-MRSA activity, in vivo toxicity and a structure–activity relationship study of a quinoline thiourea
inferred← citeshttps://doi.org/10.1016/j.bmcl.2016.12.065openalex-snapshot
Synthesis and nematicidal activities of 1,2,3-benzotriazin-4-one derivatives containing thiourea and acylthiourea against Meloidogyne incognita
inferred← citeshttps://doi.org/10.1016/j.carres.2009.09.002openalex-snapshot
Synthesis of N-tetra-O-acetyl-β-d-glucopyranosyl-N′-(4′,6′-diarylpyrimidin-2′-yl)thioureas
inferred← citeshttps://doi.org/10.1016/j.catcom.2011.06.022openalex-snapshot
Sulfated tungstate: A green catalyst for synthesis of thiomorpholides via Willgerodt–Kindler reaction
inferred← citeshttps://doi.org/10.1016/j.chemphys.2014.01.009openalex-snapshot
Competing intramolecular NHOC hydrogen bonds and extended intermolecular network in 1-(4-chlorobenzoyl)-3-(2-methyl-4-oxopentan-2-yl) thiourea analyzed by experimental and theoretical methods
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.09.059openalex-snapshot
Design, synthesis, kinetic mechanism and molecular docking studies of novel 1-pentanoyl-3-arylthioureas as inhibitors of mushroom tyrosinase and free radical scavengers
inferred← citeshttps://doi.org/10.1016/j.jcrysgro.2022.126869openalex-snapshot
Effect of trace sodium polystyrene sulfonate on the solubility, nucleation and crystallization of thiourea from metastable zone width data
inferred← citeshttps://doi.org/10.1016/j.jiec.2014.06.003openalex-snapshot
Adsorption thermodynamics and kinetics of N , N ′-diisopropoxypropyl- N ″, N ‴-oxydiethylenedicarbonyl bis (thiourea) on chalcopyrite surfaces
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2020.121115openalex-snapshot
Antibacterial and molecular study of thiourea derivative ligand and its Dimethyltin(IV) complex with the superior of its Copper(II) complex as a hepatocellular antitumor drug
inferred← citeshttps://doi.org/10.1016/j.molstruc.2003.11.029openalex-snapshot
Structural and spectral studies on N-(4-chloro)benzoyl-N′-(4-tolyl)thiourea
inferred← citeshttps://doi.org/10.1016/j.molstruc.2005.03.046openalex-snapshot
Structures and vibrational spectra of the N-benzoyl N′-dialkylthiourea derivative and their complexes with Hg(II)
inferred← citeshttps://doi.org/10.1016/j.molstruc.2018.10.055openalex-snapshot
Thioureas and their cyclized derivatives: Synthesis, conformational analysis and antimicrobial evaluation
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.135086openalex-snapshot
Novel thiourea derivative compounds: Thermal behavior, biological evaluation, Hirshfeld surfaces and frontier orbitals analyses, in silico ADMET profiling and molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.poly.2022.115786openalex-snapshot
Di- and tetra-nuclear oxorhenium(V) complexes of benzoylthiourea derivative ligands: Synthesis, structural characterization, and catalytic applications
inferred← citeshttps://doi.org/10.1016/j.reactfunctpolym.2024.106062openalex-snapshot
Synthesis and chemical recycling investigations of polythioureas
inferred← citeshttps://doi.org/10.1016/j.saa.2005.09.016openalex-snapshot
Normal coordinate analysis and crystal structure of N,N-dimethyl-N′-(2-chloro-benzoyl)thiourea
inferred← citeshttps://doi.org/10.1016/j.tet.2017.06.024openalex-snapshot
Convenient domino synthesis of quinazolin-4(3H)-ylidene carbothioamides and carbamothioates
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130575openalex-snapshot
Willgerodt-Kindler reaction at room temperature: Synthesis of thioamides from aromatic aldehydes and cyclic secondary amines
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134645openalex-snapshot
Electrophilic thiocyanation of aromatic, heteroaromatic and aliphatic compounds: A novel perspective on recent advances
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134756openalex-snapshot
Transition metal-free direct C(sp2)-H thiocyanation of 2-iminothiazolines at room temperature
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.07.212openalex-snapshot
A convenient method for the synthesis of substituted thioureas
inferred← citeshttps://doi.org/10.1016/j.vibspec.2003.09.006openalex-snapshot
Structure and vibration spectra of N-4-chlorobenzoyl–N′-4-methoxylphenylthiourea
inferred← citeshttps://doi.org/10.1016/j.vibspec.2004.03.002openalex-snapshot
Structure and vibrational spectra of the thiourea derivative and its complex with Ni(II)
inferred← citeshttps://doi.org/10.1016/s0040-4020(99)00386-5openalex-snapshot
The chemistry of thiocyanic esters
inferred← citeshttps://doi.org/10.1016/s0040-4020(99)01026-1openalex-snapshot
1-(Methyldithiocarbonyl)imidazole: a Useful Thiocarbonyl Transfer Reagent for Synthesis of Substituted Thioureas
inferred← citeshttps://doi.org/10.1016/s0040-4039(99)00093-3openalex-snapshot
A high-yielding and facile preparation of N-substituted thioureas by substitution of nitrosothioureas with alkylamines
inferred← citeshttps://doi.org/10.1016/s0065-2725(08)60129-4openalex-snapshot
Thioureas in the Synthesis of Heterocycles
inferred← citeshttps://doi.org/10.1016/s0968-0896(99)00294-1openalex-snapshot
Synthesis of C2-symmetric guanidino-sugars as potent inhibitors of glycosidases
inferred← citeshttps://doi.org/10.1021/acs.chemmater.4c03430openalex-snapshot
Decomposition of Selenourea in Various Solvents: Red versus Gray Selenium in the Synthesis of Iron Selenide Nanoparticles
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.5c03855openalex-snapshot
Sulfur Precursor Conversion Pathways in Phase Control of Cu 2– x S Nanocrystals
inferred← citeshttps://doi.org/10.1021/acs.jced.5c00034openalex-snapshot
Determination of Thiourea Solubility in 12 Different Monosolvents and Its Comparison with Structurally Similar Substances: Solvent Effect Analysis, Molecular Simulation, and Model Correlation
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00728openalex-snapshot
Easy S-Alkylation of Arylthioureas and 2-Mercaptobenzothiazoles Using Tetraalkylammonium Salts under Transition-Metal-Free Conditions
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00082openalex-snapshot
Synthesis of Dimeric Lewis A and Lewis B–Lewis A Tumor-Associated Carbohydrate Antigen Oligosaccharide Fragments
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00995openalex-snapshot
Lewis Acid-Mediated Isothiocyanation and Chlorination of Quinoxalin-2(1H)-ones under Visible Light Conditions
inferred← citeshttps://doi.org/10.1021/acs.joc.6c01314openalex-snapshot
Base-Promoted Three-Component N-Thiocarbamidation of Amines: Access to Unsymmetrical Thioureas via EDA Complexes
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02103openalex-snapshot
Isothiocyanyl Alanine as a Synthetic Intermediate for the Synthesis of Thioureayl Alanines and Subsequent Aminotetrazolyl Alanines
inferred← citeshttps://doi.org/10.1021/acs.jpclett.5b00091openalex-snapshot
Reversible Switching of Tb(III) Emission by Sensitization from 2,3-Dihydroxynaphthalene in an Isothermally Reversible Ionic Liquid
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c02821openalex-snapshot
Development of a HAT Reagent for the Decarboxylative Thiocyanation of Aliphatic Carboxylic Acids
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c00858openalex-snapshot
En Route to N -α-Silylated Thioureas via Iridium-Catalyzed C(sp 3 )–H Silylation
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00819openalex-snapshot
Thiocarbonyl Surrogate via Combination of Sulfur and Chloroform for Thiocarbamide and Oxazolidinethione Construction
inferred← citeshttps://doi.org/10.1021/cm101316hopenalex-snapshot
In situ Formation of Thermally Stable, Room-Temperature Ionic Liquids from CS2 and Amidine/Amine Mixtures.
inferred← citeshttps://doi.org/10.1021/co400102vopenalex-snapshot
Solid-Phase Synthesis of Peptide Thioureas and Thiazole-Containing Macrocycles through Ru-Catalyzed Ring-Closing Metathesis
inferred← citeshttps://doi.org/10.1021/jm0508888openalex-snapshot
Structure−Activity Study of Brassinin Derivatives as Indoleamine 2,3-Dioxygenase Inhibitors
inferred← citeshttps://doi.org/10.1021/jo035680dopenalex-snapshot
1-(Alkyl/Arylthiocarbamoyl)benzotriazoles as Stable Isothiocyanate Equivalents: Synthesis of Di- and Trisubstituted Thioureas
inferred← citeshttps://doi.org/10.1021/jo050670topenalex-snapshot
Benzotriazole-Assisted Thioacylation
inferred← citeshttps://doi.org/10.1021/jo1001593openalex-snapshot
A Concise Synthesis of Substituted Thiourea Derivatives in Aqueous Medium
inferred← citeshttps://doi.org/10.1021/jp900115gopenalex-snapshot
Reversibly Cross-Linking Amino-Polysiloxanes by Simple Triatomic Molecules. Facile Methods for Tuning Thermal, Rheological, and Adhesive Properties
inferred← citeshttps://doi.org/10.1021/la026639topenalex-snapshot
Primary Alkyl Amines as Latent Gelators and Their Organogel Adducts with Neutral Triatomic Molecules
inferred← citeshttps://doi.org/10.1021/la0343829openalex-snapshot
Detection of Pre-Sol Aggregation and Carbon Dioxide Scrambling in Alkylammonium Alkylcarbamate Gelators by Nuclear Magnetic Resonance
inferred← citeshttps://doi.org/10.1038/s41429-020-00399-7openalex-snapshot
Design, synthesis, characterization, and biological evaluation of nicotinoyl thioureas as antimicrobial and antioxidant agents
inferred← citeshttps://doi.org/10.1039/b821320hopenalex-snapshot
From simple, neutral triatomic molecules to complex chemistry
inferred← citeshttps://doi.org/10.1039/c2ra23257jopenalex-snapshot
A non-isothiocyanate route to synthesize trisubstituted thioureas of arylamines using in situ generated dithiocarbamates
inferred← citeshttps://doi.org/10.1039/c3ra46270fopenalex-snapshot
A highly efficient one-pot method for the synthesis of thioureas and 2-imino-4-thiazolidinones under microwave conditions
inferred← citeshttps://doi.org/10.1039/c4ra04628eopenalex-snapshot
Cerium ammonium nitrate-catalyzed aerobic oxidative coupling of dithiocarbamates: facile synthesis of thioureas and bis(aminothiocarbonyl)disulfides
inferred← citeshttps://doi.org/10.1039/c5ra07886eopenalex-snapshot
Design, syntheses and evaluation of benzoylthioureas as urease inhibitors of agricultural interest
inferred← citeshttps://doi.org/10.1039/c6gc00089dopenalex-snapshot
Synthesis of monosubstituted thioureas by vapour digestion and mechanochemical amination of thiocarbamoyl benzotriazoles
inferred← citeshttps://doi.org/10.1039/c8nj03077dopenalex-snapshot
Mechanistic investigation of the sulfur precursor evolution in the synthesis of highly photoluminescent Cd 0.15 Zn 0.85 S quantum dots
inferred← citeshttps://doi.org/10.1039/c8ob00239hopenalex-snapshot
Synthesis of thioureido peptidomimetics employing alkyl azides and dithiocarbamates
inferred← citeshttps://doi.org/10.1039/c8qo00752gopenalex-snapshot
Unprecedented thiocarbamidation of nitroarenes: a facile one-pot route to unsymmetrical thioureas
inferred← citeshttps://doi.org/10.1039/d0ce01810dopenalex-snapshot
Non-covalent interactions involving remote substituents influence the topologies of supramolecular chains featuring hydroxyl-O–H⋯O(hydroxyl) hydrogen bonding in crystals of (HOCH 2 CH 2 ) 2 NC(S)N(H)(C 6 H 4 Y-4) for Y = H, Me, Cl and NO 2
inferred← citeshttps://doi.org/10.1039/d0ra10436aopenalex-snapshot
A more sustainable isothiocyanate synthesis by amine catalyzed sulfurization of isocyanides with elemental sulfur
inferred← citeshttps://doi.org/10.1039/d1nj01827bopenalex-snapshot
Green and efficient synthesis of thioureas, ureas, primary O -thiocarbamates, and carbamates in deep eutectic solvent/catalyst systems using thiourea and urea
inferred← citeshttps://doi.org/10.1039/d2ob01018fopenalex-snapshot
Recent progress of direct thiocyanation reactions
inferred← citeshttps://doi.org/10.1039/d3cc06118copenalex-snapshot
Recent advancement in the synthesis of isothiocyanates
inferred← citeshttps://doi.org/10.1039/d4cc01666aopenalex-snapshot
Synthesis of N -β-brominated alkenyl isothiocyanates via dehydrogenation of alkyl isothiocyanates
inferred← citeshttps://doi.org/10.1039/d4md00816bopenalex-snapshot
Sulphonyl thiourea compounds containing pyrimidine as dual inhibitors of I, II, IX, and XII carbonic anhydrases and cancer cell lines: synthesis, characterization and in silico studies
inferred← citeshttps://doi.org/10.1039/d4nj01174kopenalex-snapshot
The short route to chalcogenurea-substituted 3 a ,6-epoxyisoindoles via an intramolecular Diels–Alder furan (IMDAF) reaction. Antibacterial and antifungal activity
inferred← citeshttps://doi.org/10.1039/d4nj01462fopenalex-snapshot
Novel asymmetric biscarbothioamides as Alzheimer's disease associated cholinesterase inhibitors: synthesis, biological activity, and molecular docking studies
inferred← citeshttps://doi.org/10.1039/d6ra01337fopenalex-snapshot
Synthesis, characterization, in vitro and in silico studies of novel lophine clubbed acylthioureas
inferred← citeshttps://doi.org/10.1080/00304947709458129openalex-snapshot
PHOSPHORUS, ARSENIC, SILICON AND METAL DERIVATIVES OF THIOUREA. A REVIEW
inferred← citeshttps://doi.org/10.1080/00387010.2012.720338openalex-snapshot
Synthesis and Antitumor, Antioxidant Effects Studies of N-Ethylpiperazine Substitute Thiourea Ligands and Their Copper(II) Complexes
inferred← citeshttps://doi.org/10.1080/00397911.2014.960939openalex-snapshot
Green Process Development for the Synthesis of Aliphatic Symmetrical N,N′-Disubstituted Thiourea Derivatives in Aqueous Medium
inferred← citeshttps://doi.org/10.1080/00397911.2014.963876openalex-snapshot
RETRACTED: Green Process Development for the Synthesis of Aliphatic Symmetrical N,N ′-Disubstituted Thiourea Derivatives in Aqueous Medium
inferred← citeshttps://doi.org/10.1080/00397919708003379openalex-snapshot
Lac Sulfur Assisted Synthesis of Symmetrical Thioureas
inferred← citeshttps://doi.org/10.1080/00397919808004429openalex-snapshot
Phase Transfer Catalyzed Synthesis of 1,6-Diaroyldithiohydrazodicarbonamide Derivatives
inferred← citeshttps://doi.org/10.1080/00397919808004862openalex-snapshot
Synthesis of N—Aroyl—N′—hydroxyethyl (Hydroxyphenyl) Thiourea Derivatives Under the Condition of Phase Transfer Catalysis
inferred← citeshttps://doi.org/10.1080/00958972.2024.2407665openalex-snapshot
A review of the synthesis and coordination of some lesser studied thiourea ligands bearing electronegative sulfonyl, phosphoryl and cyano substituents towards platinum group and related metal centers
inferred← citeshttps://doi.org/10.1080/01961778908046181openalex-snapshot
Isothiocyanates in Heterocyclic Synthesis
inferred← citeshttps://doi.org/10.1080/01961779408048961openalex-snapshot
Sulfur-Containing Vinyl Ethers
inferred← citeshttps://doi.org/10.1080/01961779608047892openalex-snapshot
α,β-Unsaturated Isothiocyanates
inferred← citeshttps://doi.org/10.1080/07366578408079451openalex-snapshot
Role of Thiourea in Redox Polymerization
inferred← citeshttps://doi.org/10.1080/10408347.2020.1777523openalex-snapshot
Medicinal Importance, Coordination Chemistry with Selected Metals (Cu, Ag, Au) and Chemosensing of Thiourea Derivatives. A Review
inferred← citeshttps://doi.org/10.1080/10426500500270099openalex-snapshot
Synthesis and Structure of N-Ethoxycarbonyl-N′-O-Methoxyphenylthiourea
inferred← citeshttps://doi.org/10.1080/10426507.2016.1223075openalex-snapshot
Novel self -condensation of ammonium dithiocarbamates leading to symmetrical substituted thioureas
inferred← citeshttps://doi.org/10.1080/10426509808032457openalex-snapshot
SYNTHESIS OF N-ALKYL-N-{[(TRIPHENYLPHOSPHORANYLID ENE)-AMINO]SULFONYL}THIOUREAS FROM ETHYL N-ALKYL-N'-{[(TRIPHENYL-PHOSPHORANYLIDENE)AMINO] SULFONYL)CARBAMIMIDOTHIOATES
inferred← citeshttps://doi.org/10.1080/14786410802223778openalex-snapshot
Synthesis, phytotoxic, cytotoxic, acetylcholinesterase and butrylcholinesterase activities ofN,N′-diaryl unsymmetrically substituted thioureas
inferred← citeshttps://doi.org/10.1080/15287398009529938openalex-snapshot
Toxicological aspects of chemical hazards in the rubber industry
inferred← citeshttps://doi.org/10.1080/17415990412331327369openalex-snapshot
Efficient and rapid route to thioamides via modified Willgerodt–Kindler reaction of quinaldine and picolines under microwave irradiation
inferred← citeshttps://doi.org/10.1080/17415990701245107openalex-snapshot
Reactions of carbon disulfide with N-nucleophiles
inferred← citeshttps://doi.org/10.1080/17415993.2013.834904openalex-snapshot
A review on the chemistry, coordination, structure and biological properties of 1-(acyl/aroyl)-3-(substituted) thioureas
inferred← citeshttps://doi.org/10.1080/17415993.2023.2226785openalex-snapshot
Thiourea-based low molecular-mass organogelators from (+)-dehydroabietylamine
inferred← citeshttps://doi.org/10.1080/17415993.2026.2651242openalex-snapshot
Comprehensive review on the synthesis of isothiocyanates via desulfurization
inferred← citeshttps://doi.org/10.1080/17518253.2010.486772openalex-snapshot
Uncatalyzed synthesis of thiomorpholide using polyethylene glycol as green reaction media
inferred← citeshttps://doi.org/10.1081/scc-100105882openalex-snapshot
SYNTHESIS AND BIOLOGICAL ACTIVITY OFN-AROYL-N′-SUBSTITUTED THIOUREA DERIVATIVES
inferred← citeshttps://doi.org/10.1107/s0108270112045167openalex-snapshot
1-Benzoyl-3-[(2-benzylsulfanyl)phenyl]thiourea
inferred← citeshttps://doi.org/10.1107/s1600536808043894openalex-snapshot
Perhydrobenzimidazole-2-thione
inferred← citeshttps://doi.org/10.1107/s1600536809001639openalex-snapshot
3-Chloro-N-(diphenylcarbamothioyl)benzamide
inferred← citeshttps://doi.org/10.1107/s2056989022012245openalex-snapshot
Synthesis, characterization, and crystal structures of N , N ′-bis(2-dialkylaminophenyl)thioureas
inferred← citeshttps://doi.org/10.1111/j.1476-5381.1995.tb13256.xopenalex-snapshot
Isothioureas: potent inhibitors of nitric oxide synthases with variable isoform selectivity
inferred← citeshttps://doi.org/10.1134/s1070428011010192openalex-snapshot
New transformations of 2-Aza-1,3,5-trienes by the action of t-BuOK-THF-DMSO
inferred← citeshttps://doi.org/10.1515/chem-2020-0139openalex-snapshot
Synthesis, characterization, and pharmacological evaluation of thiourea derivatives
inferred← citeshttps://doi.org/10.18510/gctl.2016.233openalex-snapshot
SYNTHESIS OF SOME NEW 1, 3-DI METHYL SUBSTITUTED GUANIDINE WITH POSSIBLE ANTIBACTERIAL AND ANTIFUNGAL ACTIVITY
inferred← citeshttps://doi.org/10.29057/icbi.v6i11.3035openalex-snapshot
Avances en la síntesis de Tioureas y su importancia Biológica
inferred← citeshttps://doi.org/10.29130/dubited.880667openalex-snapshot
Synthesis and Biological Evaluation of Imidazole-2-thione Fused Furazan as a New Biheterocyclic Scaffold
inferred← citeshttps://doi.org/10.3109/10731199.2013.785953openalex-snapshot
Synthesis and tyrosinase inhibitory properties of novel isoquinoline urea/thiourea derivatives
inferred← citeshttps://doi.org/10.3109/14756366.2013.815178openalex-snapshot
Metal-based carboxamide-derived compounds endowed with antibacterial and antifungal activity
inferred← citeshttps://doi.org/10.3184/174751916x14682481534021openalex-snapshot
Practical synthesis of symmetrical thioureas and heterocyclic thiones in water
inferred← citeshttps://doi.org/10.3184/174751916x14760947474916openalex-snapshot
Convenient Synthesis of Unsymmetrical N,N′-disubstituted Thioureas in Water
inferred← citeshttps://doi.org/10.32571/ijct.940169openalex-snapshot
A novel nicotinoyl thiourea manganese complex: synthesis, characterization, and biological activity studies
inferred← citeshttps://doi.org/10.3390/molecules25020401openalex-snapshot
Chiral Thioureas—Preparation and Significance in Asymmetric Synthesis and Medicinal Chemistry
inferred← citeshttps://doi.org/10.3390/molecules25122816openalex-snapshot
Cytotoxicity Evaluation of Novel bis(2-aminoethyl)amine Derivatives
inferred← citeshttps://doi.org/10.3390/molecules29204906openalex-snapshot
Novel Thiourea Ligands—Synthesis, Characterization and Preliminary Study on Their Coordination Abilities
inferred← citeshttps://doi.org/10.3897/pharmacia.70.e104579openalex-snapshot
Synthesis, characterization, and antimicrobial evaluation of new Schiff bases derived from vanillic acid conjugated to heterocyclic 4H-1,2,4-triazole-3-thiol
inferred← citeshttps://doi.org/10.48175/ijarsct-28730openalex-snapshot
Biological Application of Thiourea Derivatives
inferred← citeshttps://doi.org/10.5155/eurjchem.11.4.319-323.2047openalex-snapshot
Crystal and molecular structure of bis(N-(diethylcarbamothioyl)cyclohexane carboxamido)copper(II) complex
inferred← citeshttps://doi.org/10.64808/engineeringperspective.1839259openalex-snapshot
Experimental Assessment of N-((2-Chloropyridin-3-yl) Carbamothioyl) Thiophene-2-Carboxamide in a Spark-Ignition Engine Operating on Dichloromethane – Gasoline Blend
inferred← citeshttps://doi.org/10.70675/e957cb25z70a1z496dza833zd4639995801dopenalex-snapshot
Valorisation d'acides dicarboxyliques issus de déchets organiques ménagers
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