Works matching IS 0022152X AND DT 2024 AND VI 61 AND IP 11
Results: 20
Synthesis and Anticancer Evaluation of Tryptanthrin‐1,2,3‐Triazole Hybrids.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1891, doi. 10.1002/jhet.4916
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Syntheses of 2,4‐Substituted Quinazolines via One‐Pot Three‐Component Reactions Based on Manganese Dioxide/tert‐Butyl Hydrogen Peroxide Co‐Oxidation Using Alcohols.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1882, doi. 10.1002/jhet.4913
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Synthetic Approaches Toward Imidazo‐Fused Heterocycles: A Comprehensive Review.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1807, doi. 10.1002/jhet.4910
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Arylation of 2‐Chloro‐3‐(4,6‐Diaryl‐1,3,5‐Triazin‐2‐yl) Quinolines: Formal Synthesis of 3‐(4,6‐Diaryl‐1,3,5‐Triazin‐2‐yl)‐2‐Substituted Quinolines by Suzuki–Miyaura Reaction
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1795, doi. 10.1002/jhet.4909
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Aziridine‐Functionalized 1,3,5‐Triazine Derivatives as Promising Anticancer Agents: Synthesis, DFT Study, DNA Binding Investigations and In Vitro Cytotoxic Activity.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1801, doi. 10.1002/jhet.4908
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Efficient Synthesis and Comprehensive Characterization of bis‐Pyrazole Derivatives: Including X‐Ray Crystallography and Hirshfeld Surface Analysis.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1777, doi. 10.1002/jhet.4906
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Organocatalytic[3 + 2]Cycloaddition: Synthesis of Quinazoline Containing Sulfonyl 1,2,3‐Triazoles as Potent EGFR Targeting Anti‐Breast Cancer Agents.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1762, doi. 10.1002/jhet.4905
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- Article
Iodine‐Promoted Cascade Redox Cyclization to Access 2‐Arylbenzothiazoles Using Elemental Sulfur.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1789, doi. 10.1002/jhet.4902
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Palladium‐Catalyzed Synthesis of Pyrrolo[1,2‐α]Pyrazines From N‐Phenacyl Pyrrole‐2‐Carbonitriles and Aryl Boronic Acids.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1899, doi. 10.1002/jhet.4898
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- Article
Synthesis of Novel Nitroimidazole‐Pyrazole Hybrids via an Attractive Methodology of N‐Alkylation of 4(5)‐Nitro‐1H‐imidazole.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1721, doi. 10.1002/jhet.4897
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- Article
Fused Thiazolo[2,3‐b]Quinazolinone–Chromone Hybrids: Synthesis, Characterization, In Vitro Antibacterial Activity and In Silico Screening.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1642, doi. 10.1002/jhet.4892
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Mn(III)‐Based Oxidation of (Methylene)Bis(Cyclodiamide)s. Facile Synthesis of Tetraazadispiro‐(Undecanone)s and ‐(Tridecanone)s.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1729, doi. 10.1002/jhet.4891
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Synthesis, Fluorescence Properties, Molecular Docking Studies, and Analysis of the Crystalline Structure of the Novel 5‐Imino‐7‐Aryl‐5H‐Thiazolo[3.2‐a]Pyrimidine‐6‐Carbonitrile and Its Derivatives.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1870, doi. 10.1002/jhet.4890
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Multicomponent Assembling of Aldehydes, N,N‐Dimethylbarbituric Acid, Malononitrile, and Morpholine Into Unsymmetrical Ionic Scaffold and Its Efficient Cyclization.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1752, doi. 10.1002/jhet.4888
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Synthesis of Benzofuran‐Based Hybrid Molecules: Molecular Docking and Antibacterial Activity Against Pseudomonas aeruginosa.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1653, doi. 10.1002/jhet.4887
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Discovery of Structural Diversity Guided N‐S Heterocyclic Derivatives Based on Natural Benzothiazole Alkaloids as Potential Cytotoxic Agents.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1740, doi. 10.1002/jhet.4886
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Identification, Synthesis, and Characterization of Process Related Impurities in the Synthesis of Boc‐L‐Lys(Boc)‐OSu.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1710, doi. 10.1002/jhet.4884
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Energetic Azoxy‐Coupled Tetrazoles.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1704, doi. 10.1002/jhet.4881
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Recent Development on the Heterocycles Derived From In Situ Formation of Aryl Glyoxals by Iodine/DMSO Mediated Oxidation of Methyl Ketones.
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- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1668, doi. 10.1002/jhet.4880
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Issue Information.
- Published in:
- Journal of Heterocyclic Chemistry, 2024, v. 61, n. 11, p. 1637, doi. 10.1002/jhet.4686
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- Article