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Keyword Connections - 1,2,3-triazoles Keywords

Connection Type	Connection
Journals	European journal of medicinal chemistry Molecules (Basel, Switzerland) International journal of biological macromolecules Journal of medicinal chemistry chemistry central journal Chemical biology & drug design PLoS pathogens The Journal of the Association of Physicians of India polish journal of microbiology
Research Groups	No Research Group Connected
Bibliographies	[1] Synthesis, activity and molecular modeling studies of 1,2,3-triazole derivatives from natural phenylpropanoids as new trypanocidal agents. [2] Design, synthesis, ADME prediction and pharmacological evaluation of novel benzimidazole-1,2,3-triazole-sulfonamide hybrids as antimicrobial and antiproliferative agents. [3] Efficacy of DPP4i as the Fourth Drug in the Management of Type2 Diabetes Mellitus in Asian Indians Poorly Controlled by Use of at least 3 Oral Antidiabetic Drugs. [4] Synthesis and Cytotoxic Activity of New 1,3,4-Thiadiazole Thioglycosides and 1,2,3-Triazolyl-1,3,4-Thiadiazole -glycosides. [5] Synthesis and biological evaluation of some novel 1,2,3-triazole hybrids of myrrhanone B isolated from Commiphora mukul gum resin: Identification of potent antiproliferative leads active against prostate cancer cells (PC-3). [6] Diversity, Virulence Factors, and Antifungal Susceptibility Patterns of Pathogenic and Opportunistic Yeast Species in Rock Pigeon () Fecal Droppings in Western Saudi Arabia. [7] Biological activities and in silico physico-chemical properties of 1,2,3-triazoles derived from natural bioactive alcohols [8] Acid-mediated synthesis of fully substituted 1,2,3-triazoles: Multicomponent coupling reactions, mechanistic study, synthesis of serine hydrolase inhibitor and its derivatives [9] Metal-free C-N- and N-N-bond formation: Synthesis of 1,2,3-triazoles from ketones, N-tosylhydrazines, and amines in one pot [10] Enamine/enolate-mediated organocatalytic azide- Carbonyl [3+2] cycloaddition reactions for the synthesis of densely functionalized 1,2,3-triazoles [11] Synthesis of N -acylamidines via rhodium-catalyzed reaction of nitrosobenzene derivatives with N -sulfonyl-1,2,3-triazoles [12] '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 [13] An enolate-mediated organocatalytic Azide-Ketone [3+2]-cycloaddition reaction: Regioselective high-yielding synthesis of fully decorated 1,2,3-Triazoles [14] An efficient protocol for domino one pot synthesis of 1,2,3-triazoles from natural organic acids and phenols [15] 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 [16] 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 [17] Rhodium(II)-catalyzed stereocontrolled synthesis of 2-tetrasubstituted saturated heterocycles from 1-sulfonyl-1,2,3-triazoles [18] Facile synthesis of pyrroles via Rh(II)-catalyzed transannulation of 1-tosyl-1,2,3-triazoles with silyl or alkyl enol ethers [19] 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 [20] 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 [21] Preparation of 1-hydroxypyrazoles and 1-hydroxy-1,2,3-triazoles by dealkylation of pyrazole and triazole N-oxides [22] 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. [23] Synthesis of novel (R)-4-fluorophenyl-1H-1,2,3-triazoles: A new class of α-glucosidase inhibitors. [24] Electrophilic and nucleophilic substitution in the triazole N-oxides and N-methoxytriazolium salts: Preparation of substituted 1,2,3-triazoles [25] A General Proline Catalyzed Synthesis of 4,5-Disubstituted N-Sulfonyl-1,2,3-Triazoles from 1,3-Dicarbonyl Compounds and Sulfonyl Azide. [26] New amide linked dimeric 1,2,3-triazoles bearing aryloxy scaffolds as a potent antiproliferative agents and EGFR tyrosine kinase phosphorylation inhibitors. [27] 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. [28] Copper-Catalyzed Three-Component Reaction of Alkynes, TMSN, and Ethers: Regiocontrollable Synthesis of N- and N-Oxyalkylated 1,2,3-Triazoles. [29] 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 [30] Catalyst-free facile synthesis of polycyclic indole/pyrrole substituted-1,2,3-triazoles [31] Recent Advances in Transition-Metal-Catalyzed Denitrogenative Transformations of 1,2,3-Triazoles and Related Compounds [32] Mesoionic 1,2,3-Triazoles and 1,2,3-Triazole Carbenes [33] “Click-Triazole” Coordination Chemistry: Exploiting 1,4-Disubstituted-1,2,3-Triazoles as Ligands [34] Synthesis of 1,4,5-Trisubstituted-1,2,3-triazoles by Copper-Catalyzed Cycloaddition-Coupling of Azides and Terminal Alkynes. [35] Synthesis of 1,4,5-trisubstituted-1,2,3-triazoles by copper-catalyzed cycloaddition-coupling of azides and terminal alkynes [36] 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. [37] Direct access to 1,4-disubstituted 1,2,3-triazoles through organocatalytic 1,3-dipolar cycloaddition reaction of α,β-unsaturated esters with azides [38] 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. [39] Ln[N(SiMe3)2]3-catalyzed cycloaddition of terminal alkynes to azides leading to 1,5-disubstituted 1,2,3-triazoles: new mechanistic features [40] Potassium tert-Butoxide Promoted Cycloaddition Reaction for the Synthesis of 1,5-Disubstituted 1,2,3-Triazoles from Aromatic Azides and Trimethylsilyl-Protected Alkynes [41] 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. [42] A Microwave-Assisted Click Chemistry Synthesis of 1,4-Disubstituted 1,2,3-Triazoles via a Copper(I)-Catalyzed Three-Component Reaction. [43] Selective C(sp)-H Halogenation of "Click" 4-Aryl-1,2,3-triazoles. [44] Synthesis, anti-inflammatory, bactericidal activities and docking studies of novel 1,2,3-triazoles derived from ibuprofen using click chemistry. [45] Synthesis of bi- and bis-1,2,3-triazoles by copper-catalyzed Huisgen cycloaddition: A family of valuable products by click chemistry. [46] Regioselective conversion of arenes to N-aryl-1,2,3-triazoles using C-H borylation. [47] Rhodium(II)-catalyzed intramolecular annulation of 1-sulfonyl-1,2,3-triazoles with pyrrole and indole rings: facile synthesis of N-bridgehead azepine skeletons. [48] Fused polycyclic compounds via cycloaddition of 4-(1'-cyclohexenyl)-5-iodo-1,2,3-triazoles with 4-phenyl-1,2,4-triazoline-3,5-dione: the importance of a sacrificial iodide leaving group. [49] Synthesis of 1H-1,2,3-triazoles and study of their antifungal and cytotoxicity activities. [50] μ-Hydroxyl trinuclear copper(II) clusters: reactivity and unusual formation in the three-component synthesis of 1,2,3-triazoles in aqueous media. [51] Design, synthesis, and structure-activity correlations of novel dibenzo[b,d]furan, dibenzo[b,d]thiophene, and N-methylcarbazole clubbed 1,2,3-triazoles as potent inhibitors of Mycobacterium tuberculosis. [52] 1,2,3-triazoles as conjugative pi-linkers in push-pull chromophores: importance of substituent positioning on intramolecular charge-transfer. [53] Fused polycyclic compounds via Cycloaddition of 4-(1′-Cyclohexenyl)- 5-iodo-1,2,3-triazoles with 4-phenyl-1,2,4-triazoline-3,5-dione: The importance of a sacrificial iodide leaving group [54] Design, click synthesis, anticancer screening and docking studies of novel benzothiazole-1,2,3-triazoles appended with some bioactive benzofused heterocycles [55] Click chemistry based multicomponent approach in the synthesis of spirochromenocarbazole tethered 1,2,3-triazoles as potential anticancer agents [56] Design, synthesis and in vitro anticancer evaluation of new 2h-benzo[b][1,4]thiazin-3(4h)-one based 1,2,3-Triazoles [57] Copper fluorapatite assisted synthesis of new 1,2,3-triazoles bearing a benzothiazolyl moiety and their antibacterial and anticancer activities [58] Salophen Copper(II) Complex-Assisted Click Reactions for Fast Synthesis of 1,2,3-Triazoles Based on Naphthalene-1,4-dione Scaffold, Antibacterial Evaluation, and Molecular Docking Studies [59] Click chemistry towards thermally reversible photochromic 4,5-bisthiazolyl-1,2,3-triazoles. [60] New 1-[quinolyl(4)]-1,2,3-triazoles: Synthesis and evaluation of antiinflammatory and analgesic properties. I. [61] Synthesis, characterization and biological activities of new symmetric bis-1,2,3-triazoles with click chemistry [62] Synthesis and biological evaluation of benzenesulphonamide-bearing 1,4,5-trisubstituted-1,2,3-triazoles possessing human carbonic anhydrase I, II, IV, and IX inhibitory activity [63] Biological activities and in silico physico-chemical properties of 1,2,3-triazoles derived from natural bioactive alcohols [64] ChemInform Abstract: 1,2,3-TRIAZOLES PART 2, 4-AMINO-5-AMINOMETHYL-1,2,3-TRIAZOLES [65] Formyl- and Acyl-1,2,3-Triazoles [66] Complex 1,2,3-Triazoles Related to Practical Applications [67] Amino- and Amido-1,2,3-Triazoles [68] First synthesis of both 1-aryl-4-[( E )-alk-1-enyl]-1 H -1,2,3-triazoles and 1-aryl-4-[( Z )-1-(trimethylsilyl)alk-1-enyl]-1 H -1,2,3-triazoles: assembly of π-extended 1,2,3-triazoles using a cross-coupling/click reaction sequence [69] ChemInform Abstract: First Synthesis of Both 1-Aryl-4-[(E)-alk-1-enyl]-1H-1,2,3-triazoles and 1-Aryl-4-[(Z)-1-(trimethylsilyl)alk-1-enyl]-1H-1,2,3-triazoles: Assembly of π-Extended 1,2,3-Triazoles Using a Cross-Coupling/Click Reaction Sequence. [70] Synthesis, molecular docking, and evaluation of novel bivalent pyrazolinyl-1,2,3-triazoles as potential VEGFR TK inhibitors and anti-cancer agents [71] Synthesis, characterization and cytotoxicity studies of 1,2,3-triazoles and 1,2,4-triazolo [1,5-a] pyrimidines in human breast cancer cells [72] Synthesis and anti-cancer screening of novel heterocyclic-(2H)-1,2,3-triazoles as potential anti-cancer agents [73] In-Water Synthesis of 5-Thiolated 1,2,3-Triazoles From β-Thioenaminones by Diazo Transfer Reaction. [74] Synthesis of 1,2,3,4-tetrazine 1,3-dioxides annulated with 1,2,3-triazoles and 1,2,3-triazole 1-oxides [75] Magnetic γFeO@Sh@CuO: an efficient solid-phase catalyst for reducing agent and base-free click synthesis of 1,4-disubstituted-1,2,3-triazoles. [76] A rhodium(ii) catalysed domino synthesis of azepino fused diindoles from isatin tethered N-sulfonyl-1,2,3-triazoles and indoles. [77] Discovery and characterization of the antimetabolite action of thioacetamide-linked 1,2,3-triazoles as disruptors of cysteine biosynthesis in Gram-negative bacteria. [78] Usnic Acid Enaminone-Coupled 1,2,3-Triazoles as Antibacterial and Antitubercular Agents. [79] Bioisosteric Replacement of Amide Group with 1,2,3-Triazoles in Acetaminophen Addresses Reactive Oxygen Species-Mediated Hepatotoxic Insult in Wistar Albino Rats. [80] Synthesis and characterization of 1,2,3-triazoles-linked urea hybrid sensor for selective sensing of fluoride ion [81] 1,2,3-Triazoles based 3-substituted 2-thioquinoxalines: Synthesis, anti-bacterial activities, and molecular docking studies [82] Cu(II)-Hydrazide Coordination Compound Supported on Silica Gel as an Efficient and Recyclable Heterogeneous Catalyst for Green Click Synthesis of β-Hydroxy-1,2,3-triazoles in Water. [83] Selective and Scalable Electrosynthesis of 2H-2-(Aryl)-benzo[d]-1,2,3-triazoles and Their N-Oxides by Using Leaded Bronze Cathodes [84] pseudo-four component synthesis of mono- and di-benzylated-1,2,3-triazoles derived from aniline [85] Sunlight-Assisted Photocatalytic Sustainable Synthesis of 1,4-Disubstituted 1,2,3-Triazoles and Benzimidazoles Using TiO<inf>2</inf>−Cu<inf>2</inf>(OH)PO<inf>4</inf> Under Solvent-Free Condition