Works matching DE "THIADIAZOLES"
Results: 1189
Effects of Different Unsaturated-Linker-Containing Donors on Electronic Properties of Benzobisthiadiazole-Based Copolymers.
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- Macromolecular Chemistry & Physics, 2018, v. 219, n. 2, p. 1, doi. 10.1002/macp.201700474
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The Photoelectric Properties of Polymer Acceptors Containing Oxadiazole and Thiadiazole.
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- Macromolecular Chemistry & Physics, 2017, v. 218, n. 16, p. 1, doi. 10.1002/macp.201700094
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Synthesis and Optoelectronic Properties of Benzo[1,2- b:4,5- b′]dithiophene-Based Copolymers with Conjugated 2-(2-Ethylhexyl)-3,4-dimethoxythiophene Side Chains.
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- Macromolecular Chemistry & Physics, 2016, v. 217, n. 14, p. 1586, doi. 10.1002/macp.201600076
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Improvement in Solubility and Molecular Assembly of Cyclopentadithiophene-Benzothiadiazole Polymer.
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- Macromolecular Chemistry & Physics, 2015, v. 216, n. 11, p. 1244, doi. 10.1002/macp.201500087
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Multifunctional Photoelectroactive Materials for Optoelectronic Applications Based on Thieno[3,4‐b]pyrazines and Thieno[1,2,5]thiadiazoles.
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- Chemistry - A European Journal, 2024, v. 30, n. 7, p. 1, doi. 10.1002/chem.202303590
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Degenerately Doped Semi‐Crystalline Polymers for High Performance Thermoelectrics.
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- Advanced Functional Materials, 2021, v. 31, n. 9, p. 1, doi. 10.1002/adfm.202006900
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High Solid‐State Near Infrared Emissive Organic Fluorophores from Thiadiazole[3,4‐c]Pyridine Derivatives for Efficient Simple Solution‐Processed Nondoped Near Infrared OLEDs.
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- Advanced Functional Materials, 2020, v. 30, n. 31, p. 1, doi. 10.1002/adfm.202002481
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Molecular Engineering of Donor–Acceptor Conjugated Polymer/g‐C<sub>3</sub>N<sub>4</sub> Heterostructures for Significantly Enhanced Hydrogen Evolution Under Visible‐Light Irradiation.
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- Advanced Functional Materials, 2018, v. 28, n. 47, p. N.PAG, doi. 10.1002/adfm.201804512
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Modified poly(vinyl chloride) by unique heterocyclic molecule and examine its photo-stability in existence of nano-metallic oxides.
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- Journal of Polymer Research, 2024, v. 31, n. 2, p. 1, doi. 10.1007/s10965-024-03887-8
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Combined DFT-experimental investigation and preparation of two new Thiadiazole-based Bithiophene or Fluorene containing polymers via Suzuki-Miyaura reactions.
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- Journal of Polymer Research, 2020, v. 27, n. 5, p. 1, doi. 10.1007/s10965-020-02086-5
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Novel copolyhydrazides and copolyoxadiazoles based on 1,4-phenyl linkage and 1,3,4-thiadiazole moiety in the polymer Main chain to induce glass transition and to improve the thermal stability, solubility, and antimicrobial activity.
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- Journal of Polymer Research, 2019, v. 26, n. 2, p. 1, doi. 10.1007/s10965-019-1712-x
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Synthesis of hyperbranched conjugated polymers based on 3-hexylthiophene, triphenylamine and benzo [c] [1,2,5] thiadiazole moieties: convenient synthesis through suzuki polymerization and impact of structures on optical properties.
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- Journal of Polymer Research, 2014, v. 21, n. 9, p. 1, doi. 10.1007/s10965-014-0552-y
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Nitrogen forms modulate effects of benzothiadiazole and arbutin on cucumber sugar metabolism.
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- Biologia Plantarum, 2015, v. 59, n. 4, p. 757, doi. 10.1007/s10535-015-0552-8
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Synthesis of Allobetulin 1,2,3-thiadiazole.
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- Chemistry of Natural Compounds, 2023, v. 59, n. 5, p. 1015, doi. 10.1007/s10600-023-04183-5
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Synthesis of New Ursane-Type Hybrids with Morpholinomethyl-, Dialkylamino-, and Hydroxyl-Substituted Azoles.
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- Chemistry of Natural Compounds, 2022, v. 58, n. 1, p. 65, doi. 10.1007/s10600-022-03597-x
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Synthesis and Cytotoxicity of Lupaneand Oleanane-Type Triterpenoid Conjugates with 1,3,4-Oxadiazole.
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- Chemistry of Natural Compounds, 2021, v. 57, n. 3, p. 485, doi. 10.1007/s10600-021-03393-z
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Synthesis and Antimicrobial Activity of New Drimane and Homodrimane Sesquiterpenoids with Oxadiazole and Thiadiazole Fragments.
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- Chemistry of Natural Compounds, 2020, v. 56, n. 4, p. 656, doi. 10.1007/s10600-020-03115-x
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Synthesis, antimicrobial and antioxidant activities of 5-((2-oxo-2 H-chromen-7-yloxy)methyl)-1,3,4-thiadiazol-2(3 H)-one derived from umbelliferone.
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- Chemistry of Natural Compounds, 2013, v. 48, n. 6, p. 950, doi. 10.1007/s10600-013-0436-0
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Crystalsolvates of N-(3-ethylthio-1,2,4-thiadiazol-5-yl-aminocarbonylmethyl)cytisine.
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- Chemistry of Natural Compounds, 2008, v. 44, n. 4, p. 466, doi. 10.1007/s10600-008-9098-8
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Shoot development and plant regeneration from protocorm-like bodies of Zygopetalum mackayi.
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- In Vitro Cellular & Developmental Biology Plant, 2010, v. 46, n. 3, p. 306, doi. 10.1007/s11627-009-9262-2
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- Article
Assessment of pharmacological activity and bioavailability of the new derivative 1,3,4-thiadiazole.
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- Research Results in Pharmacology, 2018, v. 4, n. 2, p. 27, doi. 10.3897/rrpharmacology.4.27582
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- Article
Sunlight‐Driven Synthesis of 1,2,4‐Thiadiazoles via Oxidative Construction of a Nitrogen‐Sulfur Bond Catalyzed by a Reusable Covalent Organic Framework.
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- ChemPhotoChem, 2020, v. 4, n. 6, p. 445, doi. 10.1002/cptc.201900263
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Photophysics of a Bis‐Furan‐Functionalized 4,7‐bis(Phenylethynyl)‐2,1,3‐benzothiadiazole: A Building Block for Dynamic Polymers.
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- ChemPhotoChem, 2019, v. 3, n. 1, p. 54, doi. 10.1002/cptc.201800149
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SYNTHETIC APPROACHES, CHEMICAL MODIFICATION AND BIOLOGICAL ACTIVITY OF NON-CONDENSED 1,3,4-THIADIAZOLE DERIVATIVES: A REVIEW.
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- Pharmacia (0428-0296), 2018, v. 65, n. 4, p. 72
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- Article
A metal-organic capsule self-assembled by hydrogen bonds for adsorption of methylene blue.
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- Supramolecular Chemistry, 2023, v. 34, n. 3/4, p. 148, doi. 10.1080/10610278.2023.2260042
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Supramolecular assemblies tailored by dipyridyl-1,2-4-thiadiazoles: influence of the building blocks in the predictability of the final network.
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- Supramolecular Chemistry, 2020, v. 32, n. 4, p. 267, doi. 10.1080/10610278.2020.1749275
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1,1-Dichloropolyfluoroalkanesulfenamides and Their Dehydrochlorination Effected by Triethylamine.
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- Russian Journal of Organic Chemistry, 2005, v. 41, n. 2, p. 268, doi. 10.1007/s11178-005-0155-5
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- Article
Heterocyclic Thiones and Their Analogs in Reactions of 1,3-Dipolar Cycloaddition: III. Reaction of Benzothiazole-2-thione with a Double Excess of Nitrilimine.
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- Russian Journal of Organic Chemistry, 2004, v. 40, n. 8, p. 1175, doi. 10.1023/B:RUJO.0000045901.75965.de
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Synthesis of 1,2,3-Thiadiazolo Terpenoids on the Basis of Cyclopentanonopimaric and Betulonic Acids.
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- Russian Journal of Organic Chemistry, 2004, v. 40, n. 1, p. 90, doi. 10.1023/B:RUJO.0000034915.91472.fb
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- Article
Unexpected Reaction of 2-Chloro-1-Phenylethane-1,1-dithiol with Hydrazine- A New Route to 4,5-Dihydro-1,2,3-thiadiazoles.
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- Russian Journal of Organic Chemistry, 2003, v. 39, n. 10, p. 1501, doi. 10.1023/B:RUJO.0000010570.89655.28
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- Article
Synthesis of Oxamic Acids Thiohydrazides and Carbamoyl-1,3,4-thiadiazoles.
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- Russian Journal of Organic Chemistry, 2003, v. 39, n. 8, p. 1133, doi. 10.1023/B:RUJO.0000010181.01921.77
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- Article
Design, Synthesis, and Bioactivity Evaluation of Novel 1,3,4-Thiadiazole Sulfone-Derived Compounds Incorporating an Amide Moiety as Active Antibacterial Agents.
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- Russian Journal of General Chemistry, 2024, v. 94, n. 10, p. 2789, doi. 10.1134/S1070363224100220
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Triple Bond Species in the Synthesis of Oxa(thia)diazoles and Triazoles (A Review).
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- Russian Journal of General Chemistry, 2024, v. 94, n. 5, p. 1065, doi. 10.1134/S1070363224050074
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Acyl Isothiocyanates of 2-Allyl- and 2-Benzylmaleopimarimide: Synthesis of 1,3,4-Thiadiazoles.
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- Russian Journal of General Chemistry, 2024, v. 94, n. 3, p. 514, doi. 10.1134/S1070363224030034
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Design and Synthesis of Novel 1,2,3-Triazole Containing Thiadiazole Hybrids: A Potential Cytotoxic Scaffold and Their Molecular Modelling Studies.
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- Russian Journal of General Chemistry, 2024, v. 94, n. 2, p. 419, doi. 10.1134/S1070363224020178
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- Article
Synthesis of Thia- and Selenodiazoles Based on Acetosyringone and Its Glycosides.
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- Russian Journal of General Chemistry, 2023, v. 93, p. S219, doi. 10.1134/S1070363223140013
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Synthesis of Indole-1,3,4-oxadiazole Based Sulfonyl 1,2,4-Oxadiazole Derivatives as EGFR Targeting Anticancer Agents.
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- Russian Journal of General Chemistry, 2023, v. 93, n. 11, p. 2866, doi. 10.1134/S1070363223110178
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Synthesis of Novel Antimicrobial Indazole-Linked 1,2,4-Triazolylthiadiazole and 4-Thiazolidinone Derivatives and Study of Their Molecular Modelling.
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- Russian Journal of General Chemistry, 2023, v. 93, n. 4, p. 949, doi. 10.1134/S1070363223040242
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Synthesis and Anticancer Evaluation of New Thiazole and Thiadiazole Derivatives Bearing Acetanilide Moiety.
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- Russian Journal of General Chemistry, 2022, v. 92, n. 10, p. 2132, doi. 10.1134/S1070363222100267
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- Article
Design and Synthesis of Different Aryl Substituted 1,3,4-Oxadiazole-imidazo[1,5-a]pyridine Derivatives as Anticancer Agents.
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- Russian Journal of General Chemistry, 2022, v. 92, n. 5, p. 891, doi. 10.1134/S107036322205019X
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Design, Synthesis and Cytotoxic Activity of 1,2,4-Thiadiazole Linked 1,3,4-Thiadiazole-Carbazole Derivatives.
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- Russian Journal of General Chemistry, 2021, v. 91, n. 6, p. 1105, doi. 10.1134/S1070363221060189
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Synthesis and Spectral-Luminescent Properties of 2-Aryl-5-butyl-1,3,4-oxadiazoles.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 11, p. 2059, doi. 10.1134/S1070363220110079
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Microwave Assisted Synthesis and Antibacterial Activity of New 1,3,4-Thiadiazoles and 1,2,4-Triazoles Derived from 2-{2-[2-(4-Fluorophenyl)-4-methylthiazol-5-yl]-1H-benzo[d]imidazol-1-yl}acetohydrazide.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 9, p. 1721, doi. 10.1134/S1070363220090200
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Synthesis and Anticancer Activity of 1,3,4-Oxadiazole-oxazolo[4,5-b]pyridine Derivatives.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 7, p. 1331, doi. 10.1134/S107036322007021X
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Synthesis, in vitro and in silico Anti-Proliferative Studies of Novel Piperiene-Oxadiazole and Thiadiazole Analogs.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 11, p. 2301, doi. 10.1134/S1070363219110227
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- Article
Synthesis and Spectral-Luminescent Properties of 2,5-Diaryl-1,3,4-oxadiazoles and Their Chelate Complexes with Cadmium(II).
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- Russian Journal of General Chemistry, 2019, v. 89, n. 10, p. 2165, doi. 10.1134/S107036321910030X
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- Article
Reactions of Ethyl 5-Methyl-4-(1,2,3-thiadiazol-4-yl)furan-2-carboxylate with Selected Bases.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 10, p. 2147, doi. 10.1134/S1070363219100256
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- Article
Design, Synthesis and Anticancer Activity of 1,2,4-Thiadiazole Derivatives Bearing 1,2,4-Oxadiazole.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 8, p. 1696, doi. 10.1134/S1070363219080243
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Microwave Assisted Synthesis and Antimicrobial Activity of Novel 1,3,4-Thiadiazoles and 1,2,4-Triazoles Derived from 2-(3-Fluorophenyl)-4-methylthiazole-5-carbohydrazide.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 7, p. 1535, doi. 10.1134/S1070363219070259
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- Article
Synthesis and Anticancer Evaluation of Amide Derivatives of 1,3,4-Oxadiazole Linked with Benzoxazole.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 5, p. 1003, doi. 10.1134/S1070363219050219
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