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Recent advances of pyrazole-containing derivatives as anti-tubercular agents

https://doi.org/10.1016/j.ejmech.2017.07.059
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Design, synthesis and anti-tuberculosis activity of 1-adamantyl-3-heteroaryl ureas with improved in vitro pharmacokinetic properties
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Synthesis and pharmacological evaluation of nucleoside prodrugs designed to target siderophore biosynthesis in Mycobacterium tuberculosis
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Discovery of new leads against Mycobacterium tuberculosis using scaffold hopping and shape based similarity
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Design, synthesis and evaluation against Mycobacterium tuberculosis of azole piperazine derivatives as dicyclotyrosine (cYY) mimics
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Design, synthesis and biological evaluation of novel bicyclic β-lactams as potential antimalarials
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Synthesis and antitubercular activity of 2-hydroxy-aminoalkyl derivatives of diaryloxy methano phenanthrenes
inferredcites →https://doi.org/10.1016/j.bmcl.2005.08.053openalex-snapshot
A small library of trisubstituted pyrimidines as antimalarial and antitubercular agents
inferredcites →https://doi.org/10.1016/j.bmcl.2006.01.122openalex-snapshot
Anti-Plasmodium activity of imidazole–dioxolane compounds
inferredcites →https://doi.org/10.1016/j.bmcl.2007.02.078openalex-snapshot
Evaluation of N-(phenylmethyl)-4-[5-(phenylmethyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridin-4-yl]benzamide inhibitors of Mycobacterium tuberculosis growth
inferredcites →https://doi.org/10.1016/j.bmcl.2008.09.096openalex-snapshot
Clubbed [1,2,3] triazoles by fluorine benzimidazole: A novel approach to H37Rv inhibitors as a potential treatment for tuberculosis
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Peptide deformylase inhibitors of Mycobacterium tuberculosis: Synthesis, structural investigations, and biological results
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inferredcites →https://doi.org/10.1016/j.bmcl.2010.08.046openalex-snapshot
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Discovery of novel antitubercular 3a,4-dihydro-3H-indeno[1,2-c]pyrazole-2-carboxamide/carbothioamide analogues
inferredcites →https://doi.org/10.1016/j.bmcl.2011.10.057openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmcl.2012.05.063openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmcl.2012.06.072openalex-snapshot
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Design and synthesis of positional isomers of 5 and 6-bromo-1-[(phenyl)sulfonyl]-2-[(4-nitrophenoxy)methyl]-1H-benzimidazoles as possible antimicrobial and antitubercular agents
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Studies on substituted benzo[h]quinazolines, benzo[g]indazoles, pyrazoles, 2,6-diarylpyridines as anti-tubercular agents
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Synthesis and biological evaluation of 2-aminothiazole derivatives as antimycobacterial and antiplasmodial agents
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4,5-Dihydro-1H-pyrazolo[3,4-d]pyrimidine containing phenothiazines as antitubercular agents
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Synthesis and antimycobacterial activities of some new thiazolylhydrazone derivatives
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Synthesis and biological evaluation of substituted 4,6-diarylpyrimidines and 3,5-diphenyl-4,5-dihydro-1H-pyrazoles as anti-tubercular agents
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Scaffold-switching: An exploration of 5,6-fused bicyclic heteroaromatics systems to afford antituberculosis activity akin to the imidazo[1,2-a]pyridine-3-carboxylates
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2-Butyl-4-chloroimidazole based substituted piperazine-thiosemicarbazone hybrids as potent inhibitors of Mycobacterium tuberculosis
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Modified calanolides incorporated with furan-2-nitro mimics against Mycobacterium tuberculosis
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Nanomolar inhibitors of Mycobacterium tuberculosis glutamine synthetase 1: Synthesis, biological evaluation and X-ray crystallographic studies
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Synthesis, antimycobacterial evaluation and pharmacophore modeling of analogues of the natural product formononetin
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Synthesis and evaluation of novel fluorinated pyrazolo-1,2,3-triazole hybrids as antimycobacterial agents
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Whole cell screen based identification of spiropiperidines with potent antitubercular properties
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Synthesis and anti-tubercular activity of 2-nitroimidazooxazines with modification at the C-7 position as PA-824 analogs
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One-pot synthesis of new triazole—Imidazo[2,1-b][1,3,4]thiadiazole hybrids via click chemistry and evaluation of their antitubercular activity
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New INH–pyrazole analogs: Design, synthesis and evaluation of antitubercular and antibacterial activity
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Synthesis of biscoumarin and dihydropyran derivatives with promising antitumor and antibacterial activities
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Antimycobacterial activity of new N1-[1-[1-aryl-3-[4-(1H-imidazol-1-yl)phenyl]-3-oxo]propyl]-pyridine-2-carboxamidrazone derivatives
inferredcites →https://doi.org/10.1016/j.bmcl.2016.06.082openalex-snapshot
Preparation, biological evaluation and molecular docking study of imidazolyl dihydropyrimidines as potential Mycobacterium tuberculosis dihydrofolate reductase inhibitors
inferredcites →https://doi.org/10.1016/j.bmcl.2016.08.045openalex-snapshot
One pot Click chemistry: A three component reaction for the synthesis of 2-mercaptobenzimidazole linked coumarinyl triazoles as anti-tubercular agents
inferredcites →https://doi.org/10.1016/j.bmcl.2016.09.043openalex-snapshot
Identification and optimization of a new series of anti-tubercular quinazolinones
inferredcites →https://doi.org/10.1016/j.bmcl.2016.11.003openalex-snapshot
Discovery of new chemical entities as potential leads against Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1016/j.bmcl.2016.11.084openalex-snapshot
Recent advancements in the development of anti-tuberculosis drugs
inferredcites →https://doi.org/10.1016/j.bmcl.2017.03.069openalex-snapshot
6-Nitro-2,3-dihydroimidazo[2,1-b][1,3]thiazoles: Facile synthesis and comparative appraisal against tuberculosis and neglected tropical diseases
inferredcites →https://doi.org/10.1016/j.bmcl.2017.05.081openalex-snapshot
Identification and synthesis of novel inhibitors of mycobacterium ATP synthase
inferredcites →https://doi.org/10.1016/j.bmcl.2017.07.067openalex-snapshot
2-N-Arylthiazole inhibitors of Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1016/j.bmcl.2018.01.031openalex-snapshot
Design, synthesis, SAR and biological investigation of 3-(carboxymethyl)rhodanine and aminothiazole inhibitors of Mycobacterium tuberculosis Zmp1
inferredcites →https://doi.org/10.1016/j.cclet.2012.11.007openalex-snapshot
Molecular iodine catalyzed synthesis of tetrazolo[1,5-a]-quinoline based imidazoles as a new class of antimicrobial and antituberculosis agents
inferredcites →https://doi.org/10.1016/j.cclet.2015.11.001openalex-snapshot
N-Oxide heterocycles and imidazoles replacing ring D of calanolides against Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1016/j.cclet.2016.07.032openalex-snapshot
Isatin hybrids and their anti-tuberculosis activity
inferredcites →https://doi.org/10.1016/j.cell.2017.06.025openalex-snapshot
Development of a Novel Lead that Targets M. tuberculosis Polyketide Synthase 13
inferredcites →https://doi.org/10.1016/j.ejbas.2017.11.001openalex-snapshot
Synthesis and evaluation of antimicrobial, antitubercular and anticancer activities of benzimidazole derivatives
inferredcites →https://doi.org/10.1016/j.ejmech.2004.05.005openalex-snapshot
Ring-substituted imidazoles as a new class of anti-tuberculosis agents
inferredcites →https://doi.org/10.1016/j.ejmech.2004.06.014openalex-snapshot
Synthesis and anti-tuberculosis activity of N-aryl-C-nitroazoles
inferredcites →https://doi.org/10.1016/j.ejmech.2008.10.004openalex-snapshot
Synthesis, anti-tuberculosis activity and 3D-QSAR study of amino acid conjugates of 4-(adamantan-1-yl) group containing quinolines
inferredcites →https://doi.org/10.1016/j.ejmech.2008.12.001openalex-snapshot
SAR study of clubbed [1,2,4]-triazolyl with fluorobenzimidazoles as antimicrobial and antituberculosis agents
inferredcites →https://doi.org/10.1016/j.ejmech.2009.02.013openalex-snapshot
Synthesis and antitubercular screening of imidazole derivatives☆
inferredcites →https://doi.org/10.1016/j.ejmech.2009.03.027openalex-snapshot
Synthesis and antitubercular activity of novel 4-substituted imidazolyl-2,6-dimethyl-N3,N5-bisaryl-1,4-dihydropyridine-3,5-dicarboxamides
inferredcites →https://doi.org/10.1016/j.ejmech.2009.05.021openalex-snapshot
Synthesis and evaluation of in vitro anti-microbial and anti-tubercular activity of 2-styryl benzimidazoles
inferredcites →https://doi.org/10.1016/j.ejmech.2010.01.024openalex-snapshot
Novel quinoline and naphthalene derivatives as potent antimycobacterial agents
inferredcites →https://doi.org/10.1016/j.ejmech.2010.04.022openalex-snapshot
New quinoline derivatives: Synthesis and investigation of antibacterial and antituberculosis properties
inferredcites →https://doi.org/10.1016/j.ejmech.2010.04.027openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2010.11.023openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2011.01.053openalex-snapshot
Synthesis and antimycobacterial activity of prodrugs of indeno[2,1-c]quinoline derivatives
inferredcites →https://doi.org/10.1016/j.ejmech.2011.02.003openalex-snapshot
Synthesis, antibacterial and antimycobacterial activities of some new 4-aryl/heteroaryl-2,6-dimethyl-3,5-bis-N-(aryl)-carbamoyl-1,4-dihydropyridines
inferredcites →https://doi.org/10.1016/j.ejmech.2011.03.039openalex-snapshot
New quinolin-4-yl-1,2,3-triazoles carrying amides, sulphonamides and amidopiperazines as potential antitubercular agents
inferredcites →https://doi.org/10.1016/j.ejmech.2011.05.044openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2011.05.045openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2011.06.037openalex-snapshot
Novel aryloxy azolyl chalcones with potent activity against Mycobacterium tuberculosis H37Rv
inferredcites →https://doi.org/10.1016/j.ejmech.2011.07.033openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2011.09.035openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2012.01.007openalex-snapshot
Synthesis and evaluation of anti-tubercular and antibacterial activities of new 4-(2,6-dichlorobenzyloxy)phenyl thiazole, oxazole and imidazole derivatives. Part 2
inferredcites →https://doi.org/10.1016/j.ejmech.2012.03.033openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2012.08.039openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2012.10.047openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2013.03.027openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2013.06.025openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2013.08.036openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2013.10.034openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2013.10.069openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2013.10.079openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2013.11.002openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2013.12.037openalex-snapshot
Microwave induced three-component synthesis and antimycobacterial activity of benzopyrazolo[3,4-b]quinolindiones
inferredcites →https://doi.org/10.1016/j.ejmech.2014.01.039openalex-snapshot
Benzimidazole-based compounds kill Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1016/j.ejmech.2014.02.015openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2014.04.017openalex-snapshot
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inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.ejmech.2014.06.019openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2014.06.071openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2014.07.008openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2014.07.052openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2014.07.066openalex-snapshot
Structure and evaluation of antibacterial and antitubercular properties of new basic and heterocyclic 3-formylrifamycin SV derivatives obtained via ‘click chemistry’ approach
inferredcites →https://doi.org/10.1016/j.ejmech.2014.10.031openalex-snapshot
Synthesis and evaluation of in vitro antimycobacterial activity of novel 1H-benzo[d]imidazole derivatives and analogues
inferredcites →https://doi.org/10.1016/j.ejmech.2014.10.079openalex-snapshot
Synthesis, molecular docking and anti-mycobacterial evaluation of new imidazo[1,2-a]pyridine-2-carboxamide derivatives
inferredcites →https://doi.org/10.1016/j.ejmech.2014.11.042openalex-snapshot
New 1-phenyl-5-(1H-pyrrol-1-yl)-1H-pyrazole-3-carboxamides inhibit hepatitis C virus replication via suppression of cyclooxygenase-2
inferredcites →https://doi.org/10.1016/j.ejmech.2015.03.024openalex-snapshot
Synthesis and biological evaluation of new imidazo[2,1-b][1,3,4]thiadiazole-benzimidazole derivatives
inferredcites →https://doi.org/10.1016/j.ejmech.2015.03.045openalex-snapshot
Synthesis and in vitro antiplasmodial evaluation of 7-chloroquinoline–chalcone and 7-chloroquinoline–ferrocenylchalcone conjugates
inferredcites →https://doi.org/10.1016/j.ejmech.2015.05.048openalex-snapshot
Discovery of antitubercular 2,4-diphenyl-1H-imidazoles from chemical library repositioning and rational design
inferredcites →https://doi.org/10.1016/j.ejmech.2015.11.027openalex-snapshot
Synthesis and biological evaluation of novel phosphoramidate derivatives of coumarin as chitin synthase inhibitors and antifungal agents
inferredcites →https://doi.org/10.1016/j.ejmech.2016.03.061openalex-snapshot
Structure–activity relationship studies of new rifamycins containing l -amino acid esters as inhibitors of bacterial RNA polymerases
inferredcites →https://doi.org/10.1016/j.ejmech.2016.05.032openalex-snapshot
Discovery of in vitro antitubercular agents through in silico ligand-based approaches
inferredcites →https://doi.org/10.1016/j.ejmech.2016.05.043openalex-snapshot
Synthetic strategy and antiviral evaluation of diamide containing heterocycles targeting dengue and yellow fever virus
inferredcites →https://doi.org/10.1016/j.ejmech.2016.06.042openalex-snapshot
Engineering another class of anti-tubercular lead: Hit to lead optimization of an intriguing class of gyrase ATPase inhibitors
inferredcites →https://doi.org/10.1016/j.ejmech.2016.07.001openalex-snapshot
Design, synthesis and biological evaluation of novel azaspiro analogs of linezolid as antibacterial and antitubercular agents
inferredcites →https://doi.org/10.1016/j.ejmech.2016.07.009openalex-snapshot
Repurposing of a drug scaffold: Identification of novel sila analogues of rimonabant as potent antitubercular agents
inferredcites →https://doi.org/10.1016/j.ejmech.2016.09.023openalex-snapshot
Structure-activity relationship (SAR) study and design strategies of nitrogen-containing heterocyclic moieties for their anticancer activities
inferredcites →https://doi.org/10.1016/j.ejmech.2016.09.030openalex-snapshot
Pyrazolo[1,5-a]pyridine-3-carboxamide hybrids: Design, synthesis and evaluation of anti-tubercular activity
inferredcites →https://doi.org/10.1016/j.ejmech.2016.12.042openalex-snapshot
Synthesis and SAR evaluation of novel thioridazine derivatives active against drug-resistant tuberculosis
inferredcites →https://doi.org/10.1016/j.ejmech.2016.12.059openalex-snapshot
Discovery of novel anti-angiogenesis agents. Part 6: Multi-targeted RTK inhibitors
inferredcites →https://doi.org/10.1016/j.ejmech.2017.04.002openalex-snapshot
Isoniazid derivatives and their anti-tubercular activity
inferredcites →https://doi.org/10.1016/j.ejmech.2017.05.004openalex-snapshot
Recent developments of coumarin-containing derivatives and their anti-tubercular activity
inferredcites →https://doi.org/10.1016/j.ejmech.2017.05.021openalex-snapshot
Synthesis and structure-activity relationships of novel fused ring analogues of Q203 as antitubercular agents
inferredcites →https://doi.org/10.1016/j.ejmech.2017.05.026openalex-snapshot
QSAR-driven design, synthesis and discovery of potent chalcone derivatives with antitubercular activity
inferredcites →https://doi.org/10.1016/j.ejmech.2017.06.051openalex-snapshot
Triazole derivatives and their anti-tubercular activity
inferredcites →https://doi.org/10.1016/j.ejmech.2017.07.061openalex-snapshot
Quinoline hybrids and their antiplasmodial and antimalarial activities
inferredcites →https://doi.org/10.1016/j.ejmech.2017.08.025openalex-snapshot
Discovery of novel propargylamine-modified 4-aminoalkyl imidazole substituted pyrimidinylthiourea derivatives as multifunctional agents for the treatment of Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.ejmech.2017.09.050openalex-snapshot
4-Quinolone hybrids and their antibacterial activities
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.ejmech.2017.11.082openalex-snapshot
4-Quinolone derivatives and their activities against Gram positive pathogens
showing the first 200 of 298

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inferred← citeshttps://doi.org/10.1002/slct.202403478openalex-snapshot
Recent Advances in Development of Bioactive Fluorinated Pyrazole Derivatives: A Review
inferred← citeshttps://doi.org/10.1002/slct.202502109openalex-snapshot
Synthesis, Characterization, and Biological Studies of Organometallic Compounds of Re(I) with 2‐(5‐(4‐Nitrophenyl)‐3‐phenyl‐4,5‐dihydro‐1H‐pyrazol‐1‐yl)benzo[d]thiazole Based Derivatives
inferred← citeshttps://doi.org/10.1002/slct.202506991openalex-snapshot
Overview of Pyrazolo[1,5‐ a ]Pyrimidines Scaffold: Synthetic Strategies, Drug Synthesis, Structure–Activity Relationships, and Their Functional Fluorophores
inferred← citeshttps://doi.org/10.1002/slct.74747openalex-snapshot
A Review on Isatin–Acenaphthoquinone Hybrids: Emerging Multitarget Scaffolds for Antimicrobial and Anticancer Therapy
inferred← citeshttps://doi.org/10.1007/978-981-19-0832-3_7openalex-snapshot
Sulfur-Containing Pyrazoles, Pyrazolines and Indazoles
inferred← citeshttps://doi.org/10.1007/s00210-024-03524-7openalex-snapshot
Pyrazolyl amide-chalcones conjugates: Synthesis and antikinetoplastid activity
inferred← citeshttps://doi.org/10.1007/s00253-020-10606-yopenalex-snapshot
Potential anti-TB investigational compounds and drugs with repurposing potential in TB therapy: a conspectus
inferred← citeshttps://doi.org/10.1007/s10895-023-03542-3openalex-snapshot
Spectroscopic Studies on Structurally Modified Anthraquinone Azo Hydrazone Tautomer: Theoretical and Experimental Approach
inferred← citeshttps://doi.org/10.1007/s11030-023-10662-2openalex-snapshot
Structural insights and cytotoxicity evaluation of benz[e]indole pyrazolyl-substituted amides
inferred← citeshttps://doi.org/10.1007/s11030-025-11152-3openalex-snapshot
New pyrazole-based derivatives targeting MmpL3 transporter in Mycobacterium tuberculosis: design, synthesis, biological evaluation and molecular docking studies
inferred← citeshttps://doi.org/10.1007/s12039-021-01883-9openalex-snapshot
One-pot three-component condensation for the synthesis of 2,4,6-triarylpyridines and evaluation of their antimicrobial activity
inferred← citeshttps://doi.org/10.1007/s12598-023-02371-4openalex-snapshot
Engineering in amino acid‐functionalized double‐layer heteropolymolybdates: from structural control to catalytic activity
inferred← citeshttps://doi.org/10.1016/b978-0-323-85479-5.00002-2openalex-snapshot
Recent advancements on imidazole containing heterocycles as antitubercular agents
inferred← citeshttps://doi.org/10.1016/b978-0-443-15650-2.00009-xopenalex-snapshot
Role of coumarins in different infectious diseases
inferred← citeshttps://doi.org/10.1016/b978-0-443-18611-0.00028-0openalex-snapshot
Chalcones
inferred← citeshttps://doi.org/10.1016/bs.aihch.2019.01.003openalex-snapshot
The literature of heterocyclic chemistry, part XVII, 2017
inferred← citeshttps://doi.org/10.1016/j.arabjc.2021.103682openalex-snapshot
Design, synthesis, antimicrobial evaluations and in silico studies of novel pyrazol-5(4H)-one and 1H-pyrazol-5-ol derivatives
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.102969openalex-snapshot
Current development of 5-nitrofuran-2-yl derivatives as antitubercular agents
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103110openalex-snapshot
An efficient method for the synthesis of novel derivatives 4-{5-[4-(4-amino-5-mercapto-4H-[1,2,4]triazol-3-yl)-phenyl]-3-trifluoromethyl-pyrazol-1-yl}-benzenesulfonamide and their anti-inflammatory potential
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104141openalex-snapshot
Design, synthesis, molecular modeling, and biological evaluation of pyrazole-naphthalene derivatives as potential anticancer agents on MCF-7 breast cancer cells by inhibiting tubulin polymerization
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.108662openalex-snapshot
Synthesis of benzenesulfonamide tethered pyrazolyl stilbene derivatives: Their anti-proliferative and carbonic anhydrase inhibitory potentials
inferred← citeshttps://doi.org/10.1016/j.bmc.2019.04.017openalex-snapshot
Benzofuran-isatin hybrids tethered via different length alkyl linkers and their in vitro anti-mycobacterial activities
inferred← citeshttps://doi.org/10.1016/j.bmc.2025.118341openalex-snapshot
Synthesis of 1,3-diaryl substituted pyrazole-based imidazo[1,2-a]pyridine carboxamides and evaluation of their antitubercular activity
inferred← citeshttps://doi.org/10.1016/j.bmcl.2018.06.016openalex-snapshot
Azoalkyl ether imidazo[2,1-b]benzothiazoles as potentially antimicrobial agents with novel structural skeleton
inferred← citeshttps://doi.org/10.1016/j.bmcl.2018.07.046openalex-snapshot
Design, synthesis and evaluation of oxime-functionalized nitrofuranylamides as novel antitubercular agents
inferred← citeshttps://doi.org/10.1016/j.bmcl.2019.07.041openalex-snapshot
Ciprofloxacin-1,2,3-triazole-isatin hybrids tethered via amide: Design, synthesis, and in vitro anti-mycobacterial activity evaluation
inferred← citeshttps://doi.org/10.1016/j.bmcl.2020.127655openalex-snapshot
Synthesis and biological evaluation of anti-tubercular activity of Schiff bases of 2-Amino thiazoles
inferred← citeshttps://doi.org/10.1016/j.carbpol.2018.11.022openalex-snapshot
Enhanced antioxidant and antifungal activity of chitosan derivatives bearing 6-O-imidazole-based quaternary ammonium salts
inferred← citeshttps://doi.org/10.1016/j.cclet.2021.05.008openalex-snapshot
Self-assembly of a new 3D platelike ternary-oxo-cluster: An efficient catalyst for the synthesis of pyrazoles
inferred← citeshttps://doi.org/10.1016/j.cclet.2021.11.059openalex-snapshot
Two Dawson-type U(VI)-containing selenotungstates with sandwich structure and its high‐efficiency catalysis for pyrazoles
inferred← citeshttps://doi.org/10.1016/j.cclet.2022.108097openalex-snapshot
Recent advances in polyoxometalates acid-catalyzed organic reactions
inferred← citeshttps://doi.org/10.1016/j.cclet.2026.113132openalex-snapshot
A tellurotungstate hexamer based on an octanuclear cerium cluster for the synthesis of sulfonyl pyrazoles
inferred← citeshttps://doi.org/10.1016/j.cdc.2022.100977openalex-snapshot
Synthesis, characterization of some substituted Quinolines derivatives: DFT, computational, in silico ADME, molecular docking and biological activities
inferred← citeshttps://doi.org/10.1016/j.chphi.2026.101064openalex-snapshot
Spectroscopic analysis, DFT and molecular docking study of potent antibacterial agent 4- hydroxy-8-methoxyquinoline-3 carboxylic acid ethyl ester
inferred← citeshttps://doi.org/10.1016/j.cplett.2022.139469openalex-snapshot
Theoretical and experimental investigation of a pyrazole derivative- solvation effects, reactivity analysis and MD simulations
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.09.050openalex-snapshot
4-Quinolone hybrids and their antibacterial activities
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.01.078openalex-snapshot
Ciprofloxacin derivatives and their antibacterial activities
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.01.080openalex-snapshot
Fluoroquinolone derivatives and their anti-tubercular activities
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.03.016openalex-snapshot
Recent advances of imidazole-containing derivatives as anti-tubercular agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.03.037openalex-snapshot
Synthesis and anti-mitotic activity of 2,4- or 2,6-disubstituted- and 2,4,6-trisubstituted-2H-pyrazolo[4,3-c]pyridines
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.08.061openalex-snapshot
Quinolone derivatives and their activities against methicillin-resistant Staphylococcus aureus (MRSA)
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.08.095openalex-snapshot
Recent developments of quinolone-based derivatives and their activities against Escherichia coli
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.09.049openalex-snapshot
Design, synthesis and anti-mycobacterial activity evaluation of benzofuran-isatin hybrids
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.10.035openalex-snapshot
Quinoline and quinolone dimers and their biological activities: An overview
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.11.025openalex-snapshot
Benzofuran derivatives and their anti-tubercular, anti-bacterial activities
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.11.032openalex-snapshot
Fluoroquinolone-isatin hybrids and their biological activities
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.12.001openalex-snapshot
Recent advances of tetrazole derivatives as potential anti-tubercular and anti-malarial agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.12.017openalex-snapshot
Isatin derivatives and their anti-bacterial activities
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.01.017openalex-snapshot
Quinolone hybrids and their anti-cancer activities: An overview
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.01.047openalex-snapshot
Triazole derivatives and their antiplasmodial and antimalarial activities
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.2019.03.023openalex-snapshot
Tetrazole hybrids and their antifungal activities
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.04.033openalex-snapshot
1,2,4-Triazole-quinoline/quinolone hybrids as potential anti-bacterial agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.05.071openalex-snapshot
Tetrazole hybrids with potential anticancer activity
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.06.068openalex-snapshot
Nitroimidazole-containing compounds and their antibacterial and antitubercular activities
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.07.057openalex-snapshot
Synthesis and biological evaluation of moxifloxacin-acetyl-1,2,3-1H-triazole-methylene-isatin hybrids as potential anti-tubercular agents against both drug-susceptible and drug-resistant Mycobacterium tuberculosis strains
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.111587openalex-snapshot
Coumarin-containing hybrids and their anticancer activities
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.111609openalex-snapshot
Pyrazolo-benzothiazole hybrids: Synthesis, anticancer properties and evaluation of antiangiogenic activity using in vitro VEGFR-2 kinase and in vivo transgenic zebrafish model
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.111678openalex-snapshot
Benzofuran-isatin hybrids and their in vitro anti-mycobacterial activities against multi-drug resistant Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.111700openalex-snapshot
1,2,3-Triazole-containing hybrids as potential anticancer agents: Current developments, action mechanisms and structure-activity relationships
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.111744openalex-snapshot
Current scenario of tetrazole hybrids for antibacterial activity
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112967openalex-snapshot
An appraisal of anti-mycobacterial activity with structure-activity relationship of piperazine and its analogues: A review
inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.114946openalex-snapshot
Pyrimidine derivatives with antitubercular activity
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.03.018openalex-snapshot
Design, synthesis and in vitro anti-mycobacterial activities of homonuclear and heteronuclear bis-isatin derivatives
inferred← citeshttps://doi.org/10.1016/j.gresc.2023.10.004openalex-snapshot
Electrochemical cascade pyrazole annulation and C-H halogenation for the synthesis of 4-halopyrazoles
inferred← citeshttps://doi.org/10.1016/j.heliyon.2019.e01968openalex-snapshot
Synthesis, characterization and biological activities of imidazo[1,2-a]pyridine based gold(III) metal complexes
inferred← citeshttps://doi.org/10.1016/j.heliyon.2020.e05035openalex-snapshot
7-Hydroxy-4-phenyl-1, 2-dihydroquinoline derivatives: synthesis via one-pot, three-component reaction and structure elucidation
inferred← citeshttps://doi.org/10.1016/j.ica.2024.122445openalex-snapshot
Versatile CoII and NiII mononuclear complexes with furoate/thiophencarboxylate anions and 3,5-dimethylpyrazole– Synthesis, structure, magnetic, catalytic and antimycobacterial properties
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2022.122459openalex-snapshot
Synthesis of CoFe2O4 @Amino glycol/Gd nanocomposite as a high-efficiency and reusable nanocatalyst for green oxidation of sulfides and synthesis of 5-substituted 1H-tetrazoles
inferred← citeshttps://doi.org/10.1016/j.jscs.2021.101284openalex-snapshot
1,3,4-Oxadiazole-containing hybrids as potential anticancer agents: Recent developments, mechanism of action and structure-activity relationships
inferred← citeshttps://doi.org/10.1016/j.jwpe.2022.102725openalex-snapshot
Ciprofloxacin removal from non-clinical environment: A critical review of current methods and future trend prospects
inferred← citeshttps://doi.org/10.1016/j.molstruc.2018.09.073openalex-snapshot
Antibacterial study of 3-(2-amino-6-phenylpyrimidin-4-yl)-N-cyclopropyl-1-methyl-1H-indole-2-carboxamide derivatives: CoMFA, CoMSIA analyses, molecular docking and ADMET properties prediction
inferred← citeshttps://doi.org/10.1016/j.molstruc.2019.04.106openalex-snapshot
Synthesis, biological activities and docking studies of piperazine incorporated 1, 3, 4-oxadiazole derivatives
inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.127940openalex-snapshot
Synthesis, spectroscopic characterization, crystal structure, DFT, molecular docking and in vitro antibacterial potential of novel quinoline derivatives
inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.128234openalex-snapshot
Design, synthesis, antimicrobial evaluation and docking studies of urea-triazole-amide hybrids
inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.128541openalex-snapshot
Synthesis, X-ray structure, vibrational spectroscopy, DFT, biological evaluation and molecular docking studies of (E)-N’-(4-(dimethylamino)benzylidene)-5-methyl-1H-pyrazole-3-carbohydrazide
inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.129586openalex-snapshot
Synthesis, crystal structure, Hirshfeld surface analysis, biological evaluation, DFT calculations, and in silico ADME analysis of 4-arylidene pyrazolone derivatives as promising antibacterial agents
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.129982openalex-snapshot
An insight into the medicinal perspective of synthetic analogs of imidazole
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.130356openalex-snapshot
A facile one-pot, three-component synthesis of a new series of thiazolyl pyrazole carbaldehydes: In vitro anticancer evaluation, in silico ADME/T, and molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.130674openalex-snapshot
S-alkylated thiosemicarbazone derivatives: Synthesis, crystal structure determination, antimicrobial activity evaluation and molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.130863openalex-snapshot
2-(2-Amino-6-methylpyrimidin-4-yl)-4-arylmethylidene- 5-methyl-2,4-dihydro-3H-pyrazol-3-ones: Design, synthesis, structure, in vitro anti-tubercular activity, and molecular docking study
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.131067openalex-snapshot
Synthesis, crystal structure, DFT, α-glucosidase and α-amylase inhibition and molecular docking studies of (E)-N'-(4-chlorobenzylidene)-5-phenyl-1H-pyrazole-3-carbohydrazide
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.131217openalex-snapshot
Synthesis, spectroscopic characterization, DFT, molecular docking and in vitro antibacterial potential of novel quinoline derivatives
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.131473openalex-snapshot
Recent advancements and developments in search of anti-tuberculosis agents: A quinquennial update and future directions
inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.132573openalex-snapshot
New gem‑dichlorocyclopropane-pyrazole hybrids with monoterpenic skeleton: Synthesis, crystal structure, cytotoxic evaluation, molecular dynamics and theoretical study
inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.133858openalex-snapshot
Synthesis and in vitro anticancer evaluation of 8b-hydroxy-1-(6-substitutedbenzo[d]thiazol-2-yl)-3-(3-substitutedphenyl)-1,8b-dihydroindeno[1,2-c]pyrazol-4(3aH)-ones
inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.134058openalex-snapshot
DPPH and nitric oxide free radical scavenging potential of phenyl quinoline derivatives and their transition metal complexes
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.134909openalex-snapshot
One-pot sonochemical synthesis and in silico/in vitro antitubercular evaluation of 1-methyl-3-propyl-1H-pyrazole containing polynuclear fused N-heteroarenes
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.136864openalex-snapshot
Synthesis, characterization and cytotoxic activity of pyrazole derivatives based on thymol
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.137204openalex-snapshot
Synthesis, crystal and molecular structures, DFT calculations, spectroscopic (IR, NMR, UV–Vis), vibrational properties and Hirshfeld surface and antitumor activity of two pyrazole boronic acid pinacol ester compounds
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.137293openalex-snapshot
Synthesis, antimicrobial, DFT, and in silico pharmacokinetic profiling of nitroaldol quinoline derivatives: A comprehensive exploration for designing potential oral antibacterial agents targeting DNA-gyrase
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.138415openalex-snapshot
Synthesis, biological evaluation, and docking studies of pyrazole-linked benzothiazole hybrids as promising anti-TB agents
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.139579openalex-snapshot
Structural and antimicrobial activity studies of brand new benzothiazole-pyrazole conjugates
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140111openalex-snapshot
Synthesis and evaluation of the anti-TB activity of novel 7-(2-(4-substituted-phenyl)-4,5-diphenyl-1H-imidazol-1-yl)-4-methyl-2H-chromen-2-one derivatives and their DFT studies for NLO application
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.141031openalex-snapshot
Green synthesis, structural characterization, BSA binding and NLO properties of newly synthesized pyrazol-chromeno[2,3-d]pyrimidine derivative: An experimental and theoretical studies
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.141851openalex-snapshot
Synthesis, QSAR modeling, and molecular docking studies of 1,2,3-triazole-pyrazole hybrids as significant anti-cancer and anti-microbial agents
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.141875openalex-snapshot
Synthesis, DFT analysis, and molecular docking of pyrazole derivatives as targeted inhibitors of PI3K/AKT and JAK/STAT pathways in lung cancer cells
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.142405openalex-snapshot
Synthesis, DFT investigation, molecular docking, drug-likeness and molecular dynamic analysis of new quinoxaline-based pyrazoline derivatives
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.142592openalex-snapshot
Biomedical and computational exploration of rationally designed ciprofloxacin tethered β-amino alcohols as anti-cancer agents
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.143218openalex-snapshot
Pyrrolizine and pyrazole tethered spiroindolinone molecular hybrids: Synthesis, biological and molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.144410openalex-snapshot
Design, synthesis, antitubercular activity, and in silico evaluation of 2-amino benzothiazole coupled (2E)-3-phenyl-2-propenoic acid derivatives targeting Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.144646openalex-snapshot
A solvent-free Chitosan N-ium acetate-catalyzed domino/Knoevenagel- Michael-dehydrative cyclization reaction: synthesis of new pyrazolyl-xanthene‑dione scaffolds
inferred← citeshttps://doi.org/10.1016/j.mtcomm.2022.105265openalex-snapshot
Electrochemical, theoretical, and surface adsorption studies of tetrazoles analogues of amino acids in acidic media
inferred← citeshttps://doi.org/10.1016/j.poly.2022.116025openalex-snapshot
Supramolecular assemblies involving unconventional non-covalent contacts in pyrazole-based coordination compounds of Co(II) and Cu(II) pyridinedicarboxylates: Antiproliferative evaluation and theoretical studies
inferred← citeshttps://doi.org/10.1016/j.rechem.2024.101887openalex-snapshot
Non-nucleophilic base promoted synthesis of azo-linked oxazolone-pyrazole hybrids: Antimicrobial, antitubercular, anticancer evaluations and in-silico modeling insights
inferred← citeshttps://doi.org/10.1016/j.rechem.2025.102835openalex-snapshot
Enzyme-Catalysed Multicomponent Reactions (MCRs) for the Green Synthesis of Bioactive Heterocycles-A Review
inferred← citeshttps://doi.org/10.1016/j.surfin.2024.105249openalex-snapshot
Enhancing the interface stability of Li/NCM622 batteries by adding 3-trifluoromethyl pyrazole
inferred← citeshttps://doi.org/10.1016/j.tet.2018.04.030openalex-snapshot
1,3-Dipolar cycloaddition of chalcones and arylidene-1,3-dicarbonyls with diazosulfone for the regioselective synthesis of functionalized pyrazoles and pyrazolines
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130920openalex-snapshot
Transformation of arenes into 3-arylpyrazoles and 3-arylisoxazolines with β-bromopropionyl chloride, hydrazine, and hydroxylamine
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132062openalex-snapshot
A method for synthesis of polysubstituted 4-difluoromethyl and perfluoroalkyl pyrazoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151455openalex-snapshot
Silver-catalyzed synthesis of 5-aryl-3-trifluoromethyl pyrazoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154018openalex-snapshot
A zinc-catalyzed synthesis of 3-trifluoromethyl-4-trifluoroacetyl pyrazoles
inferred← citeshttps://doi.org/10.1016/j.tiv.2021.105137openalex-snapshot
Design, synthesis and biological evaluation of novel 1,2,3-triazole analogues of Imidazo-[1,2-a]-pyridine-3-carboxamide against Mycobacterium tuberculosis
inferred← citeshttps://doi.org/10.1016/j.tube.2020.101920openalex-snapshot
Drug repurposing: Fusidic acid as a potential inhibitor of M. tuberculosis FtsZ polymerization – Insight from DFT calculations, molecular docking and molecular dynamics simulations
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.2c02918openalex-snapshot
Self-Assembly of a U(VI)-Containing Polytungstate Tetramer with Lewis Acid-Base Catalytic Activity for a Dehydration Condensation Reaction
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.3c02597openalex-snapshot
Two-Fold Interpenetrated Binuclear Nickel Metal–Organic Framework as a Heterogeneous Catalyst for N-Heterocycle Synthesis
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.4c01055openalex-snapshot
Two Mn(II)-Bridged Silverton-Type [UMo12O42]8– Polyoxometalates with Catalytic Activity for the Synthesis of Pyrazoles
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00737openalex-snapshot
Collaborative Activation of Trifluoroacetyl Diazoester by a Lewis Acid and Base for the Synthesis of Polysubstituted 4-Trifluoromethylpyrazoles
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00171openalex-snapshot
Transition Metal-Free De Novo Synthesis of Sulfonated Pyrazoles from Sulfonyl Hydrazides, 1,3-Diketones, and Sodium Sulfinates at Room Temperature
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01609openalex-snapshot
Electrochemical Synthesis of Polysubstituted Sulfonated Pyrazoles via Cascade Intermolecular Condensation, Radical–Radical Cross Coupling Sulfonylation, and Pyrazole Annulation
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02122openalex-snapshot
Photocatalytic One-Pot Three-Component Reaction for the Regioselective Synthesis of Bromo-Substituted Pyrazoles
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00430openalex-snapshot
De Novo Ring-Forming Consecutive Four-Component Syntheses of 4-Pyrazolyl-1,2,3-triazoles from (Triisopropylsilyl)butadiyne as a C4 Building Block
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02897openalex-snapshot
Domino C-H Sulfonylation and Pyrazole Annulation for Fully Substituted Pyrazole Synthesis in Water Using Hydrophilic Enaminones
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02422openalex-snapshot
Aerobic Oxidative Sulfenylation of Pyrazolones and Pyrazoles Catalyzed by Metal-Free Flavin–Iodine Catalysis
inferred← citeshttps://doi.org/10.1021/acs.jpca.4c01589openalex-snapshot
The Cohesive Interactions in Phenylimidazoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02124openalex-snapshot
Synthesis of Spirobicyclic Pyrazoles by Intramolecular Dipolar Cycloadditions/[1s, 5s] Sigmatropic Rearrangements
inferred← citeshttps://doi.org/10.1021/acsomega.0c01323openalex-snapshot
2D-QSAR Modeling and Molecular Docking Studies on 1 H -Pyrazole-1-carbothioamide Derivatives as EGFR Kinase Inhibitors
inferred← citeshttps://doi.org/10.1021/acsomega.1c02093openalex-snapshot
Triethylammonium Hydrogen Sulfate [Et3NH][HSO4]-Catalyzed Rapid and Efficient Multicomponent Synthesis of Pyrido[2,3-d]pyrimidine and Pyrazolo[3,4-b]pyridine Hybrids
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.3c04736openalex-snapshot
New Thiophenyl-pyrazolyl-thiazole Hybrids as DHFR Inhibitors: Design, Synthesis, Antimicrobial Evaluation, Molecular Modeling, and Biodistribution Studies
inferred← citeshttps://doi.org/10.1021/acsomega.3c07315openalex-snapshot
Design, Synthesis, Molecular Docking, and In Vitro Antibacterial Evaluation of Benzotriazole-Based β-Amino Alcohols and Their Corresponding 1,3-Oxazolidines
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/10.1038/s41598-022-17993-4openalex-snapshot
Design and synthesis of new N-thioacylated ciprofloxacin derivatives as urease inhibitors with potential antibacterial activity
inferred← citeshttps://doi.org/10.1038/s41598-022-26605-0openalex-snapshot
Preparation and catalytic application of two different nanocatalysts based on hexagonal mesoporous silica (HMS) in synthesis of tetrahydrobenzo[b]pyran and 1,4-dihydropyrano[2,3-c]pyrazole derivatives
inferred← citeshttps://doi.org/10.1038/s41598-024-57124-9openalex-snapshot
Molecular docking, molecular dynamics simulations and binding free energy studies of interactions between Mycobacterium tuberculosis Pks13, PknG and bioactive constituents of extremophilic bacteria
inferred← citeshttps://doi.org/10.1039/c8qi00678dopenalex-snapshot
Ce( iii )-Containing tungstotellurate( vi ) with a sandwich structure: an efficient Lewis acid–base catalyst for the condensation cyclization of 1,3-diketones with hydrazines/hydrazides or diamines
inferred← citeshttps://doi.org/10.1039/c8ra01994kopenalex-snapshot
An efficient and green approach for the synthesis of 2,4-dihydropyrano[2,3- c ]pyrazole-3-carboxylates using Bi 2 O 3 /ZrO 2 as a reusable catalyst
inferred← citeshttps://doi.org/10.1039/c9ce01196jopenalex-snapshot
Systematic investigation of hydrogen-bond propensities for informing co-crystal design and assembly
inferred← citeshttps://doi.org/10.1039/c9ob00903eopenalex-snapshot
SO 2 F 2 mediated transformation of pyrazolones into pyrazolyl fluorosulfates
inferred← citeshttps://doi.org/10.1039/c9ra01590fopenalex-snapshot
Continuous-flow synthesis of 3,5-disubstituted pyrazoles via sequential alkyne homocoupling and Cope-type hydroamination
inferred← citeshttps://doi.org/10.1039/c9ra02910aopenalex-snapshot
Fe 3 O 4 /SO 3 H@zeolite-Y as a novel multi-functional and magnetic nanocatalyst for clean and soft synthesis of imidazole and perimidine derivatives
inferred← citeshttps://doi.org/10.1039/d0ob00050gopenalex-snapshot
Synthesis of 4-chalcogenyl pyrazoles via electrophilic chalcogenation/cyclization of α,β-alkynic hydrazones
inferred← citeshttps://doi.org/10.1039/d1ob00274kopenalex-snapshot
Regioselective synthesis of functionalized pyrazole-chalcones via a base mediated reaction of diazo compounds with pyrylium salts
inferred← citeshttps://doi.org/10.1039/d1qi00485aopenalex-snapshot
Self-assembly of Keggin-type U( vi )-containing tungstophosphates with a sandwich structure: an efficient catalyst for the synthesis of sulfonyl pyrazoles
inferred← citeshttps://doi.org/10.1039/d1ra07484aopenalex-snapshot
Ultrasound assisted synthesis of hybrid quinoline-imidazole derivatives: a green synthetic approach
inferred← citeshttps://doi.org/10.1039/d2cc01051hopenalex-snapshot
The largest Se-4f cluster incorporated polyoxometalate with high Lewis acid–base catalytic activity
inferred← citeshttps://doi.org/10.1039/d2ob01647hopenalex-snapshot
Facile construction of C , N -disulfonated 5-amino pyrazoles through an iodine-catalyzed cascade reaction
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