Works about TRIAZOLES
Results: 2367
Characterization of a Coumarin-Substituted 1,2,4-Oxadiazole as a Novel Antifungal Agent.
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- Bios, 2024, v. 95, p. 209, doi. 10.1893/1943-6289-95.S1.196
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- Article
Efficacy and safety of triazoles versus echinocandins in the treatment of invasive aspergillosis: A meta-analysis.
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- Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2020, v. 77, n. 9, p. 974, doi. 10.2298/VSP180528168U
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- Article
Spectroscopic Studies on the Interaction of Fluorine Containing Triazole with Bovine Serum Albumin.
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- Biological Trace Element Research, 2010, v. 138, n. 1-3, p. 125, doi. 10.1007/s12011-010-8630-4
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- Article
Regioselective Synthesis of β-Aryl Enaminones and 1,4,5- Trisubstituted 1,2,3-Triazoles from Chalcones and Benzyl Azides.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 16, p. 3347, doi. 10.1002/adsc.201400315
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- Article
Palladium-Catalyzed Acylation of 2-Aryl-1,2,3-triazoles with Aldehydes.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 5, p. 961, doi. 10.1002/adsc.201300912
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- Article
Nickel- or Palladium-Catalyzed Stereoselective Synthesis of Tetrasubstituted Olefinic Indolines-Fused Triazoles: Extension to the Spiroindoline Core.
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- Advanced Synthesis & Catalysis, 2013, v. 355, n. 18, p. 3679, doi. 10.1002/adsc.201300760
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- Article
Copper(I)-Catalyzed Aerobic Oxidative Azide-Alkene Cyclo- addition: An Efficient Synthesis of Substituted 1,2,3-Triazoles.
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- Advanced Synthesis & Catalysis, 2013, v. 355, n. 14/15, p. 2918, doi. 10.1002/adsc.201300344
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- Article
An Abnormal N-Heterocyclic Carbene-Copper(I) Complex in Click Chemistry.
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- Advanced Synthesis & Catalysis, 2013, v. 355, n. 14/15, p. 2982, doi. 10.1002/adsc.201300343
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- Article
Preparation of 1,4,5-Trisubstituted 5-Acyl-1,2,3-triazoles by Selective Acylation between Copper(I)-Carbon( sp) and Copper(I)-Carbon( sp<sup>2</sup>) Bonds with Acyl Chlorides.
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- Advanced Synthesis & Catalysis, 2013, v. 355, n. 13, p. 2564, doi. 10.1002/adsc.201300307
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- Article
In Vitro Interaction of Geldanamycin with Triazoles and Echinocandins Against Common and Emerging Candida Species.
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- Mycopathologia, 2019, v. 184, n. 5, p. 607, doi. 10.1007/s11046-019-00370-7
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- Article
Human Cutaneous Protothecosis: A Case Report and Review of Cases from Mainland China, Hong Kong, and Taiwan.
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- Mycopathologia, 2018, v. 183, n. 5, p. 821, doi. 10.1007/s11046-018-0292-3
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- Article
Molecular Identification of Candida Species Isolated from Onychomycosis in Shanghai, China.
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- Mycopathologia, 2015, v. 180, n. 5/6, p. 365, doi. 10.1007/s11046-015-9927-9
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- Article
Low temperature heat capacity of the coordination compound.
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- Journal of Thermal Analysis & Calorimetry, 2004, v. 75, n. 1, p. 331, doi. 10.1023/B:JTAN.0000017353.24441.25
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- Article
Thermal behaviour of poly(allyl azide).
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- Journal of Thermal Analysis & Calorimetry, 2003, v. 71, n. 2, p. 467, doi. 10.1023/A:1022843607664
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- Article
Synthesis of 1-(4-methylsulfone-phenyl)-5-(4-fluoro-phenyl)-5-[<sup>14</sup>C]-1,2,3-triazole and 1-(4-sulfonamide-phenyl)-5-(4-fluoro-phenyl)-5-[<sup>14</sup>C]-1,2,3-triazole as novel carbon-14 anticonvulsant.
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- Journal of Radioanalytical & Nuclear Chemistry, 2006, v. 268, n. 3, p. 545, doi. 10.1007/s10967-006-0203-9
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- Article
Triazoles and Other N-Containing Metabolites from the Marine-Derived Endophytic Fungus Penicillium chrysogenum EN-118.
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- Helvetica Chimica Acta, 2013, v. 96, n. 4, p. 682, doi. 10.1002/hlca.201200433
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- Article
New Selenosemicarbazides Derived from Imidazole-Based Carbohydrazides.
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- Helvetica Chimica Acta, 2013, v. 96, n. 3, p. 397, doi. 10.1002/hlca.201200620
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- Article
A One-Pot Tandem Ugi Multicomponent Reaction (MCR)/Click Reaction as an Efficient Protecting-Group-Free Route to 1 H-1,2,3-Triazole-Modified α-Amino Acid Derivatives and Peptidomimetics.
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- Helvetica Chimica Acta, 2012, v. 95, n. 1, p. 87, doi. 10.1002/hlca.201100253
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- Article
CuMediated Selective NArylation of Aminotriazole Acyclonucleosides.
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- Helvetica Chimica Acta, 2009, v. 92, n. 8, p. 1503, doi. 10.1002/hlca.200900033
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- Article
Synthesis of 1,2,3Triazole Analogues of Lincomycin.
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- Helvetica Chimica Acta, 2008, v. 91, n. 10, p. 1838, doi. 10.1002/hlca.200890196
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- Article
One-Pot Three-Component Synthesis of Highly Functionalized 2,3-Dihydro-1,3-dioxo-1H,5H-pyrazolo[1,2-a][1,2,4]triazoles.
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- Helvetica Chimica Acta, 2006, v. 89, n. 6, p. 1176
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Cycloaddition Reactions of 7-Benzylidenecycloocta-1,3,5-triene with Ethenetetracarbonitrile and 4-Phenyl-3H-1,2,4-triazole-3,5(4H)-dione.
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- Helvetica Chimica Acta, 2005, v. 88, n. 7, p. 2003
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1,3-Dipolar Cycloaddition Reactions of Organic Azides with Morpholinobuta-1,3-dienes and with an a-Ethynyl-enamine.
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- Helvetica Chimica Acta, 2005, v. 88, n. 7, p. 1813
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Synthesis of Triazolo[1,5-a]triazin-7-one Derivatives and Highly Functionalized [1,2,4]Triazoles.
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- Helvetica Chimica Acta, 2003, v. 86, n. 9, p. 3204
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- Article
Alkaloids of the Flora of Siberia and Altai. XXI.* 5′-(1,2,3-Triazolyl)-Substituted Lappaconitine Derivatives.
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- Chemistry of Natural Compounds, 2015, v. 51, n. 6, p. 1142, doi. 10.1007/s10600-015-1511-5
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Synthesis and Structure of Homodrimane Sesquiterpenoids Containing 1,2,4-Triazole and Carbazole Rings.
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- Chemistry of Natural Compounds, 2015, v. 51, n. 4, p. 684, doi. 10.1007/s10600-015-1384-7
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- Article
Azidoisocyanides, New Bifunctional Reagents for Multicomponent Reactions and Biomolecule Modifications.
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- Chemistry of Natural Compounds, 2014, v. 50, n. 2, p. 197, doi. 10.1007/s10600-014-0914-z
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Synthesis and study of mutagenic properties of lupane triterpenoids containing 1,2,3-triazole fragments in the C-30 position.
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- Chemistry of Natural Compounds, 2013, v. 49, n. 4, p. 657, doi. 10.1007/s10600-013-0702-1
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- Article
Amino-Acid and Dipeptide Derivatives of 2-(6-ethyl-4-oxo-3-(4-phenyl-4 H-1,2,4-triazol-3-yl)-4 H-chromen-7-yloxy)acetic Acid.
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- Chemistry of Natural Compounds, 2005, v. 41, n. 5, p. 533, doi. 10.1007/s10600-005-0199-3
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- Article
Focused small molecule library of 5,6,7,8-tetrahydro[1,2,4]triazolo-[4,3-a]pyrazines: a brick for the house of medicinal chemistry.
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- Chemistry of Heterocyclic Compounds, 2023, v. 59, n. 6/7, p. 429, doi. 10.1007/s10593-023-03213-y
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- Article
Highly regioselective one-step synthesis of 1-benzyl-5-formyl-1,2,3-triazole-4-carboxylates.
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- Chemistry of Heterocyclic Compounds, 2023, v. 59, n. 4/5, p. 267, doi. 10.1007/s10593-023-03192-0
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- Article
N-3,3,3-Trifluoropropenyl derivatives of azoles.
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- Chemistry of Heterocyclic Compounds, 2022, v. 58, n. 2/3, p. 129, doi. 10.1007/s10593-022-03065-y
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- Article
Synthesis and analgesic activity of 1-[(1,2,3-triazol-1-yl)methyl]quinolizines based on the alkaloid lupinine.
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- Chemistry of Heterocyclic Compounds, 2021, v. 57, n. 9, p. 911, doi. 10.1007/s10593-021-03000-7
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- Article
Boron-substituted 1,2,3-triazoles (microreview).
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- Chemistry of Heterocyclic Compounds, 2021, v. 57, n. 7/8, p. 737, doi. 10.1007/s10593-021-02976-6
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- Article
Toward unsymmetrical 2,6-bistriazolylpurine nucleosides.
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- Chemistry of Heterocyclic Compounds, 2021, v. 57, n. 3, p. 292, doi. 10.1007/s10593-021-02906-6
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- Article
Synthesis of 2-triazolylpurine Phosphonates.
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- Chemistry of Heterocyclic Compounds, 2021, v. 57, n. 1, p. 55, doi. 10.1007/s10593-021-02867-w
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- Article
[1,2,4]Triazolo[1,5-d][1,2,4]triazines (microreview).
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- Chemistry of Heterocyclic Compounds, 2021, v. 57, n. 1, p. 7, doi. 10.1007/s10593-021-02859-w
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- Article
Synthesis and transformations of N-butyl-3(5)-nitro-1,2,4-triazoles under the conditions of acid-catalyzed alkylation of 3(5)-nitro-1H-1,2,4-triazoles with butyl alcohols.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 11, p. 1440, doi. 10.1007/s10593-020-02835-w
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- Article
Synthesis of Novel Azides and Triazoles on the Basis of 1н-Pyrazole-3(5)-Carboxylic Acids.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 2, p. 180, doi. 10.1007/s10593-020-02643-2
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Microwave-assisted Cu-catalyzed C-C bond formation: one-pot synthesis of fully substituted 1,2,3-triazoles using nonsymmetrical iodoalkynes and their biological evaluation.
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 12, p. 1161, doi. 10.1007/s10593-019-02408-6
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- Article
Synthesis, structure, and biological activity of 2,6-diazido-4-methylnicotinonitrile derivatives.
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 10, p. 964, doi. 10.1007/s10593-018-2381-0
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- Article
Synthesis of spirocyclic 3Н-pyrrol-4-amines from 2H-azirines and 1-sulfonyl-1,2,3-triazoles.
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 10, p. 946, doi. 10.1007/s10593-018-2378-8
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Design, synthesis, and biological evaluation of new 1-aryl-4-(β-D-fructopyranos-3-O-yl)methyl-1H-1,2,3-triazole derivatives.
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 6, p. 630, doi. 10.1007/s10593-018-2319-6
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Gold and silver nanoparticle-catalyzed synthesis of heterocyclic compounds.
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 3, p. 241, doi. 10.1007/s10593-018-2259-1
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- Article
Synthesis of 1,2,3-triazoles linked into chains with other carbo- and heterocycles by a reaction between β-azolyl enamines and azides.
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 2, p. 167, doi. 10.1007/s10593-018-2249-3
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- Article
Synthesis of triazolylmethyl-linked nucleoside analogs <italic>via</italic> combination of azidofuranoses with propargylated nucleobases and study on their cytotoxicity.
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 2, p. 158, doi. 10.1007/s10593-018-2248-4
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- Article
A modified Biginelli reaction toward oxygen-bridged tetrahydropyrimidines fused with substituted 1,2,4-triazole ring.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 11, p. 1261, doi. 10.1007/s10593-018-2204-3
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Purity analysis method of 1-methyl-3,5-dinitro-1 H-1,2,4-triazole.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 10, p. 1084, doi. 10.1007/s10593-017-2175-9
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- Article
Synthetic transformations of isoquinoline alkaloids: 1-( N-alkyl-1,2,3-triazol-4-yl)-6,18- endo-ethenodihydrothebainehydroquinones and triazolylnaphthohydroquinone-containing benzofuroazocines from thebaine.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 8, p. 913, doi. 10.1007/s10593-017-2145-2
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Synthesis of 5-azido-3-nitro-1 H-1,2,4-triazole by using a cyanoethyl activating group.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 6/7, p. 719, doi. 10.1007/s10593-017-2115-8
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