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Keyword Connections - azoles Keywords

Connection Type	Connection
Journals	Organic letters Molecules (Basel, Switzerland) Chemical communications (Cambridge, England) Chemosphere
Research Groups	No Research Group Connected
Bibliographies	[1] Diazole and triazole inhibition of nitrification process in return activated sludge. [2] Hyperconjugative Antiaromaticity Activates 4-Pyrazoles as Inverse-Electron-Demand Diels-Alder Dienes. [3] Asymmetric synthesis of atropisomeric pyrazole via an enantioselective reaction of azonaphthalene with pyrazolone. [4] complexes of co2 with the azoles: tetrel bonds, hydrogen bonds and other secondary interactions [5] surveillance of antifungal susceptibilities in clinical isolates of candida species at 36 hospitals in china from 2009 to 2013 [6] Synthesis and Antibacterial Activity of New Azole, Diazole and Triazole Derivatives Based on -Aminobenzoic Acid. [7] Sulfonamido-derivatives of unsubstituted carbazoles as BACE1 inhibitors. [8] Discovery of tetrahydrocarbazoles as dual pERK and pRb inhibitors. [9] Synthesis of hetero annulated isoxazolo-, pyrido- and pyrimido carbazoles: Screened for in vitro antitumor activity and structure activity relationships, a novel 2-amino-4-(3'-bromo-4'-methoxyphenyl)-8-chloro-11H-pyrimido[4,5-a]carbazole as an antitumor agent. [10] One-Pot Three-Component Synthesis of 2,4,5-Triaryl-1 H -imidazoles in the Presence of a Molecular Sieve Supported Titanium Catalyst under Mild Basic Conditions [11] Synthesis and Characterization of Fluorine-Containing Polybenzoxazoles by High-Temperature Direct Polycondensation [12] Biological activities and in silico physico-chemical properties of 1,2,3-triazoles derived from natural bioactive alcohols [13] A Novel Synthesis of Aryl- and Heteroaryl - Annulated Carbazoles: Newly Synthesized Pyrido-, Benzo[a]- and Spirooxindolinebenzo[a]-carbazols [14] Electrochemical synthesis and electrochromic properties of new conjugated polycarbazoles from di(carbazol-9-yl)-substituted triphenylamine and N-phenylcarbazole derivatives [15] PhI(OAc) <inf>2</inf> -Mediated One-Pot Synthesis and their Antibacterial Activity of Flavone and Coumarin Based Isoxazoles Under Mild Reaction Conditions [16] Diversity-oriented synthesis of pyrazoles derivatives from flavones and isoflavones leads to the discovery of promising reversal agents of fluconazole resistance in Candida albicans [17] Assessment of mixture toxicity of (tri)azoles and their hepatotoxic effects in vitro by means of omics technologies. [18] Exploring the chemistry and therapeutic potential of triazoles: A comprehensive literature review. [19] Synthesis and Characterization of Fluorine-Containing Polybenzoxazoles by High-Temperature Direct Polycondensation [20] Degradation rates of benzotriazoles and benzothiazoles under UV-C irradiation and the advanced oxidation process UV/H2O2. [21] 3,5-Diamino-1,2,4-triazoles as a novel scaffold for potent, reversible LSD1 (KDM1A) inhibitors. [22] Acid-mediated synthesis of fully substituted 1,2,3-triazoles: Multicomponent coupling reactions, mechanistic study, synthesis of serine hydrolase inhibitor and its derivatives [23] Metal-free C-N- and N-N-bond formation: Synthesis of 1,2,3-triazoles from ketones, N-tosylhydrazines, and amines in one pot [24] Enamine/enolate-mediated organocatalytic azide- Carbonyl [3+2] cycloaddition reactions for the synthesis of densely functionalized 1,2,3-triazoles [25] Synthesis of N -acylamidines via rhodium-catalyzed reaction of nitrosobenzene derivatives with N -sulfonyl-1,2,3-triazoles [26] 'Green' synthesis of 1,4-disubstituted 5-iodo-1,2,3-triazoles under neat conditions, and an efficient approach of construction of 1,4,5-trisubstituted 1,2,3-triazoles in one pot [27] An enolate-mediated organocatalytic Azide-Ketone [3+2]-cycloaddition reaction: Regioselective high-yielding synthesis of fully decorated 1,2,3-Triazoles [28] The structure of protonated 3-pyridyl-substituted 5-amino-1H-1,2,4-triazoles: An experimental and theoretical study [29] An efficient protocol for domino one pot synthesis of 1,2,3-triazoles from natural organic acids and phenols [30] Copper nanoparticles supported on agarose as a bioorganic and degradable polymer for multicomponent click synthesis of 1,2,3-triazoles under low copper loading in water [31] Diastereoselective synthesis of tetrahydrofurano- and tetrahydropyrano-dihydropyrroles containing N,O-acetal moieties via rhodium-catalyzed transannulation of N-sulfonyl-1,2,3-triazoles with oxacycloalkenes [32] Rhodium(II)-catalyzed stereocontrolled synthesis of 2-tetrasubstituted saturated heterocycles from 1-sulfonyl-1,2,3-triazoles [33] A simple and efficient synthesis of 3,4,5-trisubstituted/N-fused 1,2,4-triazoles via ceric ammonium nitrate catalyzed oxidative cyclization of amidrazones with aldehydes using polyethylene glycol as a recyclable reaction medium [34] Facile synthesis of pyrroles via Rh(II)-catalyzed transannulation of 1-tosyl-1,2,3-triazoles with silyl or alkyl enol ethers [35] Polystyrene resin-supported CuI-cryptand 22 complex: A highly efficient and reusable catalyst for three-component synthesis of 1,4-disubstituted 1,2,3-triazoles under aerobic conditions in water [36] P -toluenesulfonic acid mediated 1,3-dipolar cycloaddition of nitroolefins with NaN <inf>3</inf> for synthesis of 4-Aryl- NH -1,2,3-triazoles [37] Synthesis, characterization and application of copper oxide chitosan nanocomposite for green regioselective synthesis of [1,2,3]triazoles. [38] Reaction of 3-nitro-1,2,4-triazoles with alkylating agents. 7*. N-monoalkylation by monocyclic α-oxide polymers [39] 1,2,3-Triazolium-1-unsubstituted methanides, carbon analogues of triazole-N-oxides: A 1,3-dipole cascade from 1,2,3-triazolium-1-methanide to 1,2,4-triazinium-4-methanide: New routes to pyrrolo[1,2-c] [1,2,3]triazoles, pyrrolo[1,2-d] [1,2,4]triazines and substituted 1-aminopyrroles. Azolium 1,3-dipoles [40] Preparation of 1-hydroxypyrazoles and 1-hydroxy-1,2,3-triazoles by dealkylation of pyrazole and triazole N-oxides [41] Generation and trapping of a 1,2,3-triazolium 1-unsubstituted methanide. A carbon analogue of the azole N-oxide: Routes to pyrrolo[1,2-c][1,2,3]triazoles and substituted 1-aminopyrroles [42] Extended tandem reactions of 2H-1,2,3-triazole N-oxides with dialkyl acetylenedicarboxylates and N-phenylmaleimide: Substituted monocyclic 2,5-dihydro-1,2,3-triazines and new tetrahydrofuro[2,3-d]-1,2,3-triazoles. Azolium 1,3-dipoles. Part 5. [43] Novel Pyranopyrazoles: Synthesis and Theoretical Studies [44] Inhibition of Dimorphic Switch by Cobalt(II) Complexes with Ligands Derived from Pyrazoles and Dinitrobenzoate: Synthesis, Characterization and Biological Activity. [45] Conversion of substituted 5-aryloxypyrazolecarbaldehydes into reduced 3,4'-bipyrazoles: synthesis and characterization, and the structures of four precursors and two products, and their supramolecular assembly in zero, one and two dimensions. [46] Development of Predictive Antioxidant Models for 1,3,4-Oxadiazoles by Quantitative Structure Activity Relationship [47] Synthesis of novel (R)-4-fluorophenyl-1H-1,2,3-triazoles: A new class of α-glucosidase inhibitors. [48] In Vitro Interaction of Geldanamycin with Triazoles and Echinocandins Against Common and Emerging Candida Species. [49] Development of 3,5-Dinitrophenyl-Containing 1,2,4-Triazoles and their Trifluoromethyl Analogues as Highly Efficient Antitubercular Agents Inhibiting Decaprenylphosphoryl-β-D-ribofuranose 2'-Oxidase. [50] Preparation and application of magnetic chitosan/graphene oxide composite supported copper as a recyclable heterogeneous nanocatalyst in the synthesis of triazoles [51] Unravel the surface active sites on Cu/MgLaO solid base catalyst by DRIFT spectroscopy and adsorption techniques for the synthesis of triazoles by click reaction [52] Organic Solid Acid/NaNO2: An Efficient System for the Oxidation of Urazoles and Bis-Urazoles under Mild and Heterogeneous Conditions [53] Electrophilic and nucleophilic substitution in the triazole N-oxides and N-methoxytriazolium salts: Preparation of substituted 1,2,3-triazoles [54] Sorption of polyhalogenated carbazoles (PHCs) to microplastics. [55] Conversion of Benzimidazoles, Imidazothiazoles and Imidazoles Into More Potent Central Nervous System Acting Drugs. [56] Synthesis, biological activity and molecular modeling of a new series of condensed 1,2,4-triazoles. [57] A General Proline Catalyzed Synthesis of 4,5-Disubstituted N-Sulfonyl-1,2,3-Triazoles from 1,3-Dicarbonyl Compounds and Sulfonyl Azide. [58] Discovery of novel functionalized 1,2,4-triazoles as PARP-1 inhibitors in breast cancer: Design, synthesis and antitumor activity evaluation. [59] New amide linked dimeric 1,2,3-triazoles bearing aryloxy scaffolds as a potent antiproliferative agents and EGFR tyrosine kinase phosphorylation inhibitors. [60] Simultaneous quantification of systemic azoles and their major metabolites in human serum by HPLC/PDA: role of azole metabolic rate. [61] Complexes of (η(6)-benzene)ruthenium(II) with 1,4-bis(phenylthio/seleno-methyl)-1,2,3-triazoles: synthesis, structure and applications in catalytic activation of oxidation and transfer hydrogenation. [62] Phenothiazine and pyridine-N-oxide-based AIE-active triazoles: Synthesis, morphology and photophysical properties [63] Visible-Light-Induced Oxidation/[3 + 2] Cycloaddition/Oxidative Aromatization to Construct Benzo[]carbazoles from 1,2,3,4-Tetrahydronaphthalene and Arylhydrazine Hydrochlorides. [64] Re-sensitizing Multidrug Resistant Bacteria to Antibiotics by Targeting Bacterial Response Regulators: Characterization and Comparison of Interactions between 2-Aminoimidazoles and the Response Regulators BfmR from Acinetobacter baumannii and QseB from Francisella spp. [65] Benzyne-azide polycycloaddition: A facile route toward functional polybenzotriazoles [66] Synthesis of 1,5-disubstituted tetrazole-1,2,3 triazoles hybrids via Ugi-azide/CuAAC [67] Synthesis of polyfunctional imidazoles from vinyl azides and amidine along with NHBoc as a leaving group [68] Consecutive hydrazino-Ugi-azide reactions: synthesis of acylhydrazines bearing 1,5-disubstituted tetrazoles [69] Preparation, Characterization, and Application of Preyssler Heteropoly Acid Immobilized on Magnetic Nanoparticles as a Green and Recoverable Catalyst for the Synthesis of Imidazoles [70] CF3-Substituted Pyrazolines and Pyrazoles via Huisgen Cycloaddition [71] Pd-Catalyzed methoxylation of C(sp)-H bonds adjacent to benzoxazoles and benzothiazoles. [72] Synthesis, Characterization and Antimicrobial Activity of d Metal Complexes of some 2-Substituted-1H-Benzimidazoles. [73] Antimicrobial activity of some 2- and 3-pyridinyl-1H-benzimidazoles and their FeIII, CuII, ZnII, and AgI complexes. [74] Antimicrobial activity of FeIII, CuII, AgI, ZnII and HgII complexes of 2-(2-hydroxy-5-bromo/nitro-phenyl)-1H- and 2-(2-hydroxyphenyl)-5-methyl/chloro/nitro-1H-benzimidazoles. [75] Alternate pathway for the click reaction of 2-(2-azidophenyl)-4,5-diaryloxazoles. [76] Tailored therapeutics based on 1,2,3-1-triazoles: a mini review. [77] Copper-Catalyzed Three-Component Reaction of Alkynes, TMSN, and Ethers: Regiocontrollable Synthesis of N- and N-Oxyalkylated 1,2,3-Triazoles. [78] A click chemistry approach for the synthesis of cyclic ureido tethered coumarinyl and 1-aza coumarinyl 1,2,3-triazoles as inhibitors of Mycobacterium tuberculosis H37Rv and their in silico studies [79] Catalyst-free facile synthesis of polycyclic indole/pyrrole substituted-1,2,3-triazoles [80] Synthesis of 1,4,5-trisubstituted triazoles by [3+2] cycloaddition of a ruthenium azido complex with ynoate esters [81] Discovery of benzothiazoles as antimycobacterial agents: Synthesis, structure-activity relationships and binding studies with Mycobacterium tuberculosis decaprenylphosphoryl-β-D-ribose 2'-oxidase. [82] Recent Advances in Transition-Metal-Catalyzed Denitrogenative Transformations of 1,2,3-Triazoles and Related Compounds [83] 1,2,4-Triazoles. XXVII. Synthesis of the thiazolo [2,3-c]-s-triazole and the thiazolo[3,2-b]-s-triazole systems [84] Fragmentation de Triazoles Sous L'Impact Electronique—II 1,2,3-Triazole [85] Triazoles. Part XI. Synthesis of 1,2,4-triazole-3-sulphonic acids by oxidation of 1,2,4-triazoline-3-thiones [86] Triazoles. Part VIII. 1,2,4-Triazole-3-sulphonic acids [87] Nuclear magnetic resonance studyes of triazoles. I. Tautomerism of 1,2,4-triazole [88] ChemInform Abstract: Triazoles. Part 9. HMO Calculations of Tautomeric 1,2,4-Triazole Derivatives. [89] Mesoionic 1,2,3-Triazoles and 1,2,3-Triazole Carbenes [90] “Click-Triazole” Coordination Chemistry: Exploiting 1,4-Disubstituted-1,2,3-Triazoles as Ligands [91] Synthesis of 1,4,5-Trisubstituted-1,2,3-triazoles by Copper-Catalyzed Cycloaddition-Coupling of Azides and Terminal Alkynes. [92] Synthesis of 1,4,5-trisubstituted-1,2,3-triazoles by copper-catalyzed cycloaddition-coupling of azides and terminal alkynes [93] ChemInform Abstract: Direct Access to 1,4-Disubstituted 1,2,3-Triazoles Through Organocatalytic 1,3-Dipolar Cycloaddition Reaction of α,β-Unsaturated Esters with Azides. [94] Direct access to 1,4-disubstituted 1,2,3-triazoles through organocatalytic 1,3-dipolar cycloaddition reaction of α,β-unsaturated esters with azides [95] ChemInform Abstract: Regioselective Formation of 2,5-Disubstituted Oxazoles via Copper(I)-Catalyzed Cycloaddition of Acyl Azides and 1-Alkynes. [96] ChemInform Abstract: Ln[N(SiMe3)2]3-Catalyzed Cycloaddition of Terminal Alkynes to Azides Leading to 1,5-Disubstituted 1,2,3-Triazoles: New Mechanistic Features. [97] Ln[N(SiMe3)2]3-catalyzed cycloaddition of terminal alkynes to azides leading to 1,5-disubstituted 1,2,3-triazoles: new mechanistic features [98] RuH2(CO)(PPh3)3 Catalyzed Selective Formation of 1,4-Disubstituted Triazoles from Cycloaddition of Alkynes and Organic Azides [99] Potassium tert-Butoxide Promoted Cycloaddition Reaction for the Synthesis of 1,5-Disubstituted 1,2,3-Triazoles from Aromatic Azides and Trimethylsilyl-Protected Alkynes [100] ChemInform Abstract: Potassium tert-Butoxide Promoted Cycloaddition Reaction for the Synthesis of 1,5-Disubstituted 1,2,3-Triazoles from Aromatic Azides and Trimethylsilyl-Protected Alkynes. [101] A Microwave-Assisted Click Chemistry Synthesis of 1,4-Disubstituted 1,2,3-Triazoles via a Copper(I)-Catalyzed Three-Component Reaction.