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Synthesis and Fungicidal Activity of Novel Aminophenazine-1-carboxylate Derivatives

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/0040-4020(63)85005-xopenalex-snapshot
Phenazines-IV
inferredcites →https://doi.org/10.1016/0040-4020(63)85006-1openalex-snapshot
Phenazines—V
inferredcites →https://doi.org/10.1016/j.bmc.2005.09.032openalex-snapshot
Phenazine-1-carboxamides: Structure–cytotoxicity relationships for 9-substituents and changes in the H-bonding pattern of the cationic side chain
inferredcites →https://doi.org/10.1016/j.bmc.2008.02.031openalex-snapshot
Potent anti-prostate cancer agents derived from a novel androgen receptor down-regulating agent
inferredcites →https://doi.org/10.1016/j.tetlet.2007.09.046openalex-snapshot
Aramidocalix[4]arenes as new anion receptors
inferredcites →https://doi.org/10.1016/s0040-4020(01)99258-0openalex-snapshot
Phenazines—III
inferredcites →https://doi.org/10.1016/s0960-894x(01)00692-8openalex-snapshot
Solid-Phase synthesis of new saphenamycin analogues with antimicrobial activity
inferredcites →https://doi.org/10.1021/ja991159iopenalex-snapshot
Biosynthesis of Phenazine Antibiotics inStreptomyces antibioticus: Stereochemistry of Methyl Transfer from Carbon-2 of Acetate
inferredcites →https://doi.org/10.1021/jf902320eopenalex-snapshot
Design, Synthesis, and Fungicidal Activity of Novel Analogues of Pyrrolnitrin
inferredcites →https://doi.org/10.1021/jm00005a005openalex-snapshot
Synthesis and Anti-HIV-1 Activity of 4,5,6,7-Tetrahydro-5-methylimidazo[4,5,1-jk][1,4]benzodiazepin-2(1H)-one (TIBO) Derivatives. 3
inferredcites →https://doi.org/10.1021/jm00388a017openalex-snapshot
Potential antitumor agents. 51. Synthesis and antitumor activity of substituted phenazine-1-carboxamides
inferredcites →https://doi.org/10.1021/jm010329aopenalex-snapshot
Novel Angular Benzophenazines: Dual Topoisomerase I and Topoisomerase II Inhibitors as Potential Anticancer Agents
inferredcites →https://doi.org/10.1021/jm990423fopenalex-snapshot
Bis(phenazine-1-carboxamides): Structure−Activity Relationships for a New Class of Dual Topoisomerase I/II-Directed Anticancer Drugs
inferredcites →https://doi.org/10.1021/jo00874a008openalex-snapshot
Carbon-13 nuclear magnetic resonance chemical shifts of substituted phenazines
inferredcites →https://doi.org/10.1039/b404735bopenalex-snapshot
Marine chemical ecology
inferredcites →https://doi.org/10.1039/b702742gopenalex-snapshot
Marine chemical ecology
inferredcites →https://doi.org/10.1080/00397918708063967openalex-snapshot
Unequivocal Synthesis of Phenazine-1-Carboxylic Acids: Selective Displacement of Fluorine During Alkaline Borohydride Reduction of N-(2-Fluorophenyl)-3-Nitroanthranilic Acids

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4790365openalex-extracted
N-(3 '-Fluorobenzyl)-Phenazine-Carboxamide Efficiently Inhibits the Replication of Infectious Bronchitis Virus Via Enhancing the Phosphorylation of Eif2α, Ire1 and Erk in Cells
inferred← citeshttps://doi.org/10.1002/cmdc.202000797openalex-snapshot
Identification of Phenazine‐Based MEMO1 Small‐Molecule Inhibitors: Virtual Screening, Fluorescence Polarization Validation, and Inhibition of Breast Cancer Migration
inferred← citeshttps://doi.org/10.1002/jccs.201800355openalex-snapshot
A green approach to the synthesis of 2,3‐diaminophenazine using a photocatalytic system of CdFe2O4/TiO2 nanoparticles
inferred← citeshttps://doi.org/10.1002/slct.202203793openalex-snapshot
Synthesis and Biological Activities Assessment of 4‐, 6‐, and 9‐Phenylphenalenone Derivatives
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.07.017openalex-snapshot
Synthesis and anticancer activity of some novel 2-phenazinamine derivatives
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.12.007openalex-snapshot
Synthesis and antiproliferative activity of novel polynuclear heterocyclic compounds derived from 2,3-diaminophenazine
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113823openalex-snapshot
Anti-schistosomal activities of quinoxaline-containing compounds: From hit identification to lead optimisation
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2011.12.030openalex-snapshot
Synthesis of phenazines by Cu-catalyzed homocoupling of 2-halogen anilines in water
inferred← citeshttps://doi.org/10.1016/j.molliq.2017.08.030openalex-snapshot
Apparent thermodynamic models for determination of the solubility of N-acetyl-1,3-phenylenediamine in eight pure solvents and two different miscible systems at T= (278.15–323.15) K
inferred← citeshttps://doi.org/10.1016/j.molliq.2025.128853openalex-snapshot
Fine-tuning on the radical-mediated dimerization of o-aminophenol and o-phenylendiamine by iodosylarene derivatives: Kinetic and mechanistic DFT study
inferred← citeshttps://doi.org/10.1016/j.phytol.2023.05.011openalex-snapshot
Synthesis and biological activities of some new antimicrobial and cytotoxic 5-/7-/8-phenylphenalenone derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.10.067openalex-snapshot
An efficient catalyst-free synthesis of novel benzo[a][1,3]oxazino[6,5-c]phenazine derivatives via one pot four-component domino protocol in water
inferred← citeshttps://doi.org/10.1021/ol4026556openalex-snapshot
Total Synthesis of Thaxtomin A and Its Stereoisomers and Findings of Their Biological Activities
inferred← citeshttps://doi.org/10.1039/c3cy20798fopenalex-snapshot
Organosilver( i / ii ) catalyzed C–N coupling reactions – phenazines
inferred← citeshttps://doi.org/10.1039/c4gc00901kopenalex-snapshot
Towards the rational biosynthesis of substituted phenazines and phenoxazinones by laccases
inferred← citeshttps://doi.org/10.1186/s13065-018-0478-2openalex-snapshot
Design, synthesis and biological activity of hydroxybenzoic acid ester conjugates of phenazine-1-carboxylic acid
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