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Novel 1,2,3-Triazole Derivatives for Use against Mycobacterium tuberculosis H37Rv (ATCC 27294) Strain
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Comparative antimycobacterial activities of rifampin, rifapentine, and KRM-1648 against a collection of rifampin-resistant Mycobacterium tuberculosis isolates with known rpoB mutations
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1016/j.bmcl.2019.04.026openalex-snapshot
Ultrasonication-ionic liquid synergy for the synthesis of new potent anti-tuberculosis 1,2,4-triazol-1-yl-pyrazole based spirooxindolopyrrolizidines
inferred← citeshttps://doi.org/10.1016/j.bmcl.2019.126846openalex-snapshot
The bioisosteric modification of pyrazinamide derivatives led to potent antitubercular agents: Synthesis via click approach and molecular docking of pyrazine-1,2,3-triazoles
inferred← citeshttps://doi.org/10.1016/j.bmcl.2020.127434openalex-snapshot
Novel isoniazid embedded triazole derivatives: Synthesis, antitubercular and antimicrobial activity evaluation
inferred← citeshttps://doi.org/10.1016/j.bmcl.2020.127579openalex-snapshot
Design and synthesis of new indanol-1,2,3-triazole derivatives as potent antitubercular and antimicrobial agents
inferred← citeshttps://doi.org/10.1016/j.bmcl.2020.127746openalex-snapshot
1,2,3-triazole-thiazole hybrids: Synthesis, in vitro antimicrobial activity and antibiofilm studies
inferred← citeshttps://doi.org/10.1016/j.bmcl.2021.127984openalex-snapshot
Microwave assisted regioselective synthesis of quinoline appended triazoles as potent anti-tubercular and antifungal agents via copper (I) catalyzed cycloaddition
inferred← citeshttps://doi.org/10.1016/j.bmcl.2023.129551openalex-snapshot
Design, synthesis and antitubercular assessment of 1, 2, 3-triazole incorporated thiazolylcarboxylate derivatives
inferred← citeshttps://doi.org/10.1016/j.carres.2015.10.005openalex-snapshot
Novel triazolyl-functionalized chitosan derivatives with different chain lengths of aliphatic alcohol substituent: Design, synthesis, and antifungal activity
inferred← citeshttps://doi.org/10.1016/j.catcom.2016.12.030openalex-snapshot
Palladium-catalysed direct arylation of heteroarenes using 1-(bromophenyl)-1,2,3-triazoles as aryl source
inferred← citeshttps://doi.org/10.1016/j.cclet.2015.11.003openalex-snapshot
1,2,3-Triazole incorporated coumarin derivatives as potential antifungal and antioxidant agents
inferred← citeshttps://doi.org/10.1016/j.cclet.2016.03.014openalex-snapshot
1,2,3-Triazole tethered acetophenones: Synthesis, bioevaluation and molecular docking study
inferred← citeshttps://doi.org/10.1016/j.cdc.2020.100452openalex-snapshot
Synthesis, Characterization, Pass prediction, In-silico ADME, Molecular docking and Cyclic voltammetry studies of 1, 4, 5-trisubstituted 1, 2, 3-triazole ethanone and ethanol derivatives via Metal free approach
inferred← citeshttps://doi.org/10.1016/j.cdc.2020.100457openalex-snapshot
An efficient continuous-flow synthesis and evaluation of antimicrobial activity of novel 1,2,3-Triazole-Furan hybrid chalcone derivatives
inferred← citeshttps://doi.org/10.1016/j.dyepig.2022.110905openalex-snapshot
Newly synthesized benzothiazolyl-1,2,3-triazole derivatives: Intramolecular charge transfer tuning, solvatofluorochromism and antiproliferative properties
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.03.028openalex-snapshot
Synthesis of 3-O-propargylated betulinic acid and its 1,2,3-triazoles as potential apoptotic agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.06.042openalex-snapshot
Synthesis and evaluation of α-ketotriazoles and α,β-diketotriazoles as inhibitors of Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.12.039openalex-snapshot
1-Phenyl-1H- and 2-phenyl-2H-1,2,3-triazol derivatives: Design, synthesis and inhibitory effect on alpha-glycosidases
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.02.017openalex-snapshot
Sulfur rich 2-mercaptobenzothiazole and 1,2,3-triazole conjugates as novel antitubercular agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.03.022openalex-snapshot
Synthesis and preliminary biological evaluation of 1,2,3-triazole-Jaspine B hybrids as potential cytotoxic agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.04.052openalex-snapshot
Synthesis of novel 1,2,3-triazole substituted-N-alkyl/aryl nitrone derivatives, their anti-inflammatory and anticancer activity
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.05.005openalex-snapshot
Synthesis of novel 1,2,3-triazole derivatives of isoniazid and their in vitro and in vivo antimycobacterial activity evaluation
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.06.009openalex-snapshot
Design, synthesis and antiproliferative activity of functionalized flavone-triazole-tetrahydropyran conjugates against human cancer cell lines
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.07.061openalex-snapshot
Synthesis and antiproliferative activity of 8-hydroxyquinoline derivatives containing a 1,2,3-triazole moiety
inferred← citeshttps://doi.org/10.1016/j.ejmech.2015.10.019openalex-snapshot
A click chemistry approach for the synthesis of mono and bis aryloxy linked coumarinyl triazoles as anti-tubercular agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2015.10.024openalex-snapshot
Design, synthesis and evaluation of diarylpiperazine derivatives as potent anti-tubercular agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.07.005openalex-snapshot
Functional induction of P-glycoprotein efflux pump by phenyl benzenesulfonamides: Synthesis and biological evaluation of T0901317 analogs
inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.09.067openalex-snapshot
Synthesis, in vitro evaluation and molecular docking studies of novel triazine-triazole derivatives as potential α-glucosidase inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.09.086openalex-snapshot
Antitubercular activity of 1,2,3-triazolyl fatty acid derivatives
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.04.002openalex-snapshot
Isoniazid derivatives and their anti-tubercular activity
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.04.040openalex-snapshot
Design, combinatorial synthesis and biological evaluations of novel 3-amino-1′-((1-aryl-1 H -1,2,3-triazol-5-yl)methyl)-2′-oxospiro[benzo[ a ] pyrano[2,3- c ]phenazine-1,3′-indoline]-2-carbonitrile antitumor hybrid molecules
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.06.051openalex-snapshot
Triazole derivatives and their anti-tubercular activity
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.08.034openalex-snapshot
1-Aryl-1 H - and 2-aryl-2 H -1,2,3-triazole derivatives blockade P2X7 receptor in vitro and inflammatory response in vivo
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.10.061openalex-snapshot
Design, synthesis and biological evaluation of novel benzimidazole amidines as potent multi-target inhibitors for the treatment of non-small cell lung cancer
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.11.052openalex-snapshot
Hetero-Diels-Alder reactions of novel 3-triazolyl-nitrosoalkenes as an approach to functionalized 1,2,3-triazoles with antibacterial profile
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.01.071openalex-snapshot
New hydrazides derivatives of isoniazid against Mycobacterium tuberculosis: Higher potency and lower hepatocytotoxicity
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.07.018openalex-snapshot
Synthesis and evaluation of the cytotoxic activity of Furanaphthoquinones tethered to 1H-1,2,3-triazoles in Caco-2, Calu-3, MDA-MB231 cells
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.02.010openalex-snapshot
Molecular hybridization approach for phenothiazine incorporated 1,2,3-triazole hybrids as promising antimicrobial agents: Design, synthesis, molecular docking and in silico ADME studies
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.02.055openalex-snapshot
Comprehensive review on the anti-bacterial activity of 1,2,3-triazole hybrids
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.111974openalex-snapshot
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)
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.114064openalex-snapshot
Design, synthesis and biological evaluation of P2-modified proline analogues targeting the HtrA serine protease in Chlamydia
inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.114454openalex-snapshot
Emerging impact of triazoles as anti-tubercular agent
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2012.09.001openalex-snapshot
Nitroxides attenuate carrageenan-induced inflammation in rat paws by reducing neutrophil infiltration and the resulting myeloperoxidase-mediated damage
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2016.06.006openalex-snapshot
Synthesis of water soluble chitosan derivatives with halogeno-1,2,3-triazole and their antifungal activity
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2021.121369openalex-snapshot
Development of potent nanosized isatin-isonicotinohydrazide hybrid for management of Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1016/j.insi.2025.100094openalex-snapshot
Pharmacological potential and in silico studies of triazole derivatives: A comprehensive review
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2020.109516openalex-snapshot
Methyl-2,2-difluoro-2-(fluorosulfonyl) acetate (MDFA)/copper (I) iodide mediated and tetrabutylammonium iodide promoted trifluoromethylation of 1-aryl-4-iodo-1,2,3-triazoles
inferred← citeshttps://doi.org/10.1016/j.jscs.2019.12.001openalex-snapshot
Uracil-coumarin based hybrid molecules as potent anti-cancer and anti-bacterial agents
inferred← citeshttps://doi.org/10.1016/j.jtice.2022.104503openalex-snapshot
MnO2 nanoparticle encapsulated in polyelectrolytic hybrids from alkyl functionalized carboxymethyl cellulose and azide functionalized gelatin to treat tumors by photodynamic therapy and photothermal therapy
inferred← citeshttps://doi.org/10.1016/j.matchemphys.2022.126508openalex-snapshot
Corrosion inhibition and ecotoxicological assessment of 1,2,3-triazolic alcohols
inferred← citeshttps://doi.org/10.1016/j.mcat.2019.110523openalex-snapshot
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
inferred← citeshttps://doi.org/10.1016/j.molstruc.2019.127487openalex-snapshot
A step-by-step synthesis of triazole-benzimidazole-chalcone hybrids: Anticancer activity in human cells+
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.135163openalex-snapshot
Hydrazones tethered disubstituted 1,2,3-triazoles: Design, synthesis, antitubercular and antimicrobial evaluation
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.135619openalex-snapshot
Thiadiazole based triazole/hydrazone derivatives: Synthesis, in vitro α-glucosidase inhibitory activity and in silico molecular docking study
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.137129openalex-snapshot
New 1,2,3-triazole tethered-1,4-dihydropyridines as potential antioxidant agents: Synthesis and molecular docking study
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.137207openalex-snapshot
Three novel 1,2,3-triazole-fused compounds: Syntheses, structural and spectroscopic characterizations with molecular modeling
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.137359openalex-snapshot
Novel 4,5-dibromo-N-phenyl-1H-pyrrole-2-carboxamide Hybrids as Promising DNA Gyrase Inhibitors: Design, synthesis and antimicrobial evaluation
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140486openalex-snapshot
Microwave expedited Cu(I) catalyzed regioselective 1,2,3-triazoles as Mycobacterium Tuberculosis H37Rv inhibitors, in vitro α-amylase and α-glucosidase inhibition, in silico studies
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.146910openalex-snapshot
Multitarget isoxazole–1,2,3-triazole hybrids: From synthesis to antimicrobial, antioxidant and Culex pipiens larvicidal applications supported by molecular simulations
inferred← citeshttps://doi.org/10.1016/j.pestbp.2019.12.004openalex-snapshot
Bioactive-guided structural optimization of 1,2,3-triazole phenylhydrazones as potential fungicides against Fusarium graminearum
inferred← citeshttps://doi.org/10.1016/j.rechem.2022.100605openalex-snapshot
Design, synthesis and biological evaluation of novel substituted indazole-1,2,3-triazolyl-1,3,4-oxadiazoles: Antimicrobial activity evaluation and docking study
inferred← citeshttps://doi.org/10.1016/j.rechem.2025.102987openalex-snapshot
A3 coupling of 1,2,3-Triazoles: Microwave-enhanced catalysis with [pyridine–SO3H]CuCl3
inferred← citeshttps://doi.org/10.1016/j.steroids.2023.109258openalex-snapshot
Steroid-triazole conjugates: A brief overview of synthesis and their application as anticancer agents
inferred← citeshttps://doi.org/10.1016/j.tet.2016.11.074openalex-snapshot
Synthesis of novel glycosyl-1,2,3-1H-triazolyl methyl quinazolin-4(3H)-ones and their effect on GLUT4 translocation
inferred← citeshttps://doi.org/10.1016/j.tet.2025.135066openalex-snapshot
Design, synthesis, and pharmacological profiling of benzimidazole-based isoniazid analogues: A comprehensive investigation into antitubercular activity, molecular characterization, and computational study
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.03.108openalex-snapshot
One-pot sequential azide–alkyne/intramolecular azomethine ylide 1,3-dipolar cycloaddition strategy for the synthesis of carbohydrate grafted macrocycles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.10.023openalex-snapshot
Tandem synthesis of 1-formyl-1,2,3-triazoles
inferred← citeshttps://doi.org/10.1021/acs.cgd.7b01141openalex-snapshot
Neutral Molecular Iron(II) Complexes Showing Tunable Bistability at Above, Below, and Just Room Temperature by a Crystal Engineering Approach: Ligand Mobility into a Three-Dimensional Flexible Supramolecular Network
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.8b01418openalex-snapshot
Catalytic Nitrene Homocoupling by an Iron(II) Bis(alkoxide) Complex: Bulking Up the Alkoxide Enables a Wider Range of Substrates and Provides Insight into the Reaction Mechanism
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.8b02929openalex-snapshot
Magnetic Cationic Copper(II) Chains and a Mononuclear Cobalt(II) Complex Containing [Ln(hfac)4]− Blocks as Counterions
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.2c00432openalex-snapshot
A 1,2,3-Triazole Derivative of Quinazoline Exhibits Antitumor Activity by Tethering RNF168 to SQSTM1/P62
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00562openalex-snapshot
Stitching Triazoles to Arenes via a Transition Metal-Free Aryne Diels–Alder/1,3-Prototropic Shift/Dehydrobromination Cascade
inferred← citeshttps://doi.org/10.1021/acs.joc.6c01055openalex-snapshot
A Regioselective Azide–Alkyne Cycloaddition to 1,2,3-Triazole-4-carboxaldehydes, Polyheteroaryls, and Synthesis of Rufinamide
inferred← citeshttps://doi.org/10.1021/acs.langmuir.6c02011openalex-snapshot
Electrochemical and Theoretical Evaluation of Carbothioamide-Derived Corrosion Inhibitors for Mild Steel in Acidic Environments
inferred← citeshttps://doi.org/10.1021/acschemneuro.8b00591openalex-snapshot
Synthesis and Preliminary Evaluations of a Triazole-Cored Antagonist as a PET Imaging Probe ([18F]N2B-0518) for GluN2B Subunit in the Brain
inferred← citeshttps://doi.org/10.1021/acsomega.0c02916openalex-snapshot
Synthesis and Evaluation of Biphenyl-1,2,3-Triazol-Benzonitrile Derivatives as PD-1/PD-L1 Inhibitors
inferred← citeshttps://doi.org/10.1021/acsomega.1c03734openalex-snapshot
New 1,2,3-Triazole-Appended Bis-pyrazoles: Synthesis, Bioevaluation, and Molecular Docking
inferred← citeshttps://doi.org/10.1021/acsomega.4c03906openalex-snapshot
Synthesis, Biological Properties, and Molecular Docking Study of Novel 1,2,3-Triazole-8-quinolinol Hybrids
inferred← citeshttps://doi.org/10.1021/cr200409fopenalex-snapshot
Click Chemistry for Drug Development and Diverse Chemical–Biology Applications
inferred← citeshttps://doi.org/10.1021/jm300125eopenalex-snapshot
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
inferred← citeshttps://doi.org/10.1038/nchembio.1277openalex-snapshot
Antituberculosis thiophenes define a requirement for Pks13 in mycolic acid biosynthesis
inferred← citeshttps://doi.org/10.1039/c3gc37066fopenalex-snapshot
Synthesis of polymerizable vinyltriazoles: development of an optimized one-pot strategy starting from 4-bromobutyne
inferred← citeshttps://doi.org/10.1039/c3ob41676copenalex-snapshot
Design, synthesis and characterization of novel inhibitors against mycobacterial β-ketoacyl CoA reductase FabG4
inferred← citeshttps://doi.org/10.1039/c4md00288aopenalex-snapshot
Novel isoniazid–amidoether derivatives: synthesis, characterization and antimycobacterial activity evaluation
inferred← citeshttps://doi.org/10.1039/c4ob01758gopenalex-snapshot
Synthesis and antifungal activity of 1,2,3-triazole phenylhydrazone derivatives
inferred← citeshttps://doi.org/10.1039/c4ra14329aopenalex-snapshot
Chalcomer assembly of optical chemosensors for selective Cu 2+ and Ni 2+ ion recognition
inferred← citeshttps://doi.org/10.1039/c5md00057bopenalex-snapshot
1,2,3-Triazole derivatives as antitubercular agents: synthesis, biological evaluation and molecular docking study
inferred← citeshttps://doi.org/10.1039/c5md00404gopenalex-snapshot
Synthesis and evaluation of thieno[2,3-d]pyrimidin-4(3H)-ones as potential antitubercular agents
inferred← citeshttps://doi.org/10.1039/c5nj00679aopenalex-snapshot
Two Cu( ii ) complexes of triadimefon: crystal structure, antifungal activities and structure–activity relationship
inferred← citeshttps://doi.org/10.1039/c5nj01845eopenalex-snapshot
Synergistic actions between tebuconazole ligand and Cu( ii ) cation: reasons for the enhanced antifungal activity of four Cu( ii ) complexes based on the fungicide tebuconazole
inferred← citeshttps://doi.org/10.1039/c5ob00054hopenalex-snapshot
Synthesis of new generation triazolyl- and isoxazolyl-containing 6-nitro-2,3-dihydroimidazooxazoles as anti-TB agents: in vitro, structure–activity relationship, pharmacokinetics and in vivo evaluation
inferred← citeshttps://doi.org/10.1039/c5ra19038jopenalex-snapshot
Direct access to 1,4-disubstituted 1,2,3-triazoles through organocatalytic 1,3-dipolar cycloaddition reaction of α,β-unsaturated esters with azides
inferred← citeshttps://doi.org/10.1039/c6nj02069kopenalex-snapshot
Synthesis and evaluation of novel imidazo[4,5-c]pyridine derivatives as antimycobacterial agents against Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1039/c6nj02671kopenalex-snapshot
Identification and development of pyrazolo[4,3-c]pyridine carboxamides as Mycobacterium tuberculosis pantothenate synthetase inhibitors
inferred← citeshttps://doi.org/10.1039/c7cc09934gopenalex-snapshot
Copper-catalyzed decarboxylative regioselective synthesis of 1,5-disubstituted 1,2,3-triazoles
inferred← citeshttps://doi.org/10.1039/c7ra03629aopenalex-snapshot
Two novel Co( ii ) and Ni( ii ) complexes of tebuconazole with enhanced antifungal activities
inferred← citeshttps://doi.org/10.1039/c7tb00099eopenalex-snapshot
A facile water-stable MOF-based “off–on” fluorescent switch for label-free detection of dopamine in biological fluid
inferred← citeshttps://doi.org/10.1039/c8dt04771eopenalex-snapshot
Arylhydrazone ligands as Cu-protectors and -catalysis promoters in the azide–alkyne cycloaddition reaction
inferred← citeshttps://doi.org/10.1039/c8md00055gopenalex-snapshot
Triazole–diindolylmethane conjugates as new antitubercular agents: synthesis, bioevaluation, and molecular docking
inferred← citeshttps://doi.org/10.1039/c8md00620bopenalex-snapshot
Synthesis and discovery of asiatic acid based 1,2,3-triazole derivatives as antitumor agents blocking NF-κB activation and cell migration
inferred← citeshttps://doi.org/10.1039/c8ra03197eopenalex-snapshot
1,2,3-Triazole-fused spirochromenes as potential anti-tubercular agents: synthesis and biological evaluation
inferred← citeshttps://doi.org/10.1039/c9gc01129copenalex-snapshot
Reactions of α-haloacroleins with azides: highly regioselective synthesis of formyl triazoles
inferred← citeshttps://doi.org/10.1039/c9nj03462eopenalex-snapshot
Structural modification of zolpidem led to potent antimicrobial activity in imidazo[1,2- a ]pyridine/pyrimidine-1,2,3-triazoles
inferred← citeshttps://doi.org/10.1039/c9nj03802gopenalex-snapshot
The design and green synthesis of novel benzotriazoloquinolinyl spirooxindolopyrrolizidines: antimycobacterial and antiproliferative studies
inferred← citeshttps://doi.org/10.1039/c9qo00864kopenalex-snapshot
Reaction engineering and photophysical studies of fully enriched C -vinyl-1,2,3-triazoles
inferred← citeshttps://doi.org/10.1039/d0ob00848fopenalex-snapshot
Organocatalytic enone-azide [3 + 2]-cycloaddition: synthesis of functionally rich C / N -double vinyl 1,2,3-triazoles
inferred← citeshttps://doi.org/10.1039/d1md00387aopenalex-snapshot
Synthesis and evaluation of triazole congeners of nitro-benzothiazinones potentially active against drug resistant Mycobacterium tuberculosis demonstrating bactericidal efficacy
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