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Herbicidal indolizine‐5,8‐diones: photosystem I redox mediators
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1096-9063(199812)54:4<385::aid-ps842>3.0.co;2-copenalex-snapshot
Metabolism-related assays and their application to agrochemical research: reactivity of pesticides with glutathione and glutathione transferases†
inferredcites →https://doi.org/10.1002/(sici)1526-4998(200002)56:2<120::aid-ps112>3.0.co;2-vopenalex-snapshot
1,3,4(2H)-Isoquinolinetriones: evaluation of amino-substituted derivatives as redox mediator herbicides
inferredcites →https://doi.org/10.1002/(sici)1526-4998(200002)56:2<127::aid-ps113>3.0.co;2-lopenalex-snapshot
Synthesis and characterisation of some 4-keto derivatives of 1,3,4(2H)-isoquinolinetrione redox mediator herbicides
inferredcites →https://doi.org/10.1002/jlac.197719770115openalex-snapshot
C‐Acylierung von 5 gliedrigen N‐Heterocyclen, I. Acylierung an C‐2 von Imidazolen und Benzimidazolen
inferredcites →https://doi.org/10.1002/ps.2780440108openalex-snapshot
1,3,4(2H)‐isoquinolinetrione herbicides: Novel redox mediators of photosystem I
inferredcites →https://doi.org/10.1007/978-1-4684-8661-2_8openalex-snapshot
Effects of Substituents in Quinonoid Compounds
inferredcites →https://doi.org/10.1007/978-94-009-5548-6openalex-snapshot
The Determination of Ionization Constants
inferredcites →https://doi.org/10.1016/0045-6535(81)90211-3openalex-snapshot
The bipyridinium herbicides
inferredcites →https://doi.org/10.1016/s0040-4039(00)74750-2openalex-snapshot
Synthesis of indolizine-5,8-diones and [3.2.2]cyclazines
inferredcites →https://doi.org/10.1016/s0040-4039(01)97828-1openalex-snapshot
Reactions of squaric acid and some derivatives with thionyl chloride/,-dimethylformamide
inferredcites →https://doi.org/10.1016/s0076-6879(80)69011-9openalex-snapshot
[9] Preparation of higher plant chloroplasts
inferredcites →https://doi.org/10.1021/ja00103a021openalex-snapshot
A Method for Computing One-Electron Reduction Potentials and Its Application to p-Benzoquinone in Water at 300 K
inferredcites →https://doi.org/10.1021/ja00737a019openalex-snapshot
Ring strain effects. III. Reduction and oxidation potential shifts
inferredcites →https://doi.org/10.1021/jm00010a023openalex-snapshot
Hypoxia-Selective Agents Derived from Quinoxaline 1,4-Di-N-oxides
inferredcites →https://doi.org/10.1021/jo00246a016openalex-snapshot
Synthesis of 4-substituted-3-alkoxy-3-cyclobutene-1,2-diones
inferredcites →https://doi.org/10.1021/jo00365a043openalex-snapshot
A general, regiospecific synthesis of highly substituted quinones
inferredcites →https://doi.org/10.1039/p19900001463openalex-snapshot
Pyrrolo[1,2-b]isoquinoline-5,10-diones and indolizine-5,8-diones
inferredcites →https://doi.org/10.1055/s-1978-24652openalex-snapshot
Die präparative Chemie der Cyclobutendione; I. Synthese von Cyclobutendion und dessen Alkyl-, Alkenyl-und Aryl-Derivaten
inferredcites →https://doi.org/10.1055/s-1978-24841openalex-snapshot
Die präparative Chemie der Cyclobutendione; II. Reaktionen von Alkyl-, Alkenyl- und Arylcyclobutendionen
inferredcites →https://doi.org/10.1055/s-1978-24920openalex-snapshot
Die präparative Chemie der Cyclobutendione; III. Synthese von Quadratsäure, Benzocyclobutendion und deren Derivaten
inferredcites →https://doi.org/10.1055/sos-sd-010-00982openalex-snapshot
Product Class 16: Indolizines
inferredcites →https://doi.org/10.1063/1.555843openalex-snapshot
Reduction Potentials of One-Electron Couples Involving Free Radicals in Aqueous Solution
inferredcites →https://doi.org/10.1246/bcsj.49.1157openalex-snapshot
Syntheses of 3,4-Dimethylpyrrole
inferredcites →https://doi.org/10.2307/2530789openalex-snapshot
Encyclopedia of Statistical Sciences 2.
inferredcites →https://doi.org/10.5860/choice.30-3265openalex-snapshot
Physiology of herbicide action
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.4676491openalex-extracted
Synthesis of Novel Π-Extended 2,5-Disubstituted Indolizines and Their Photophysical Properties
inferred← citeshttps://doi.org/10.1002/9781444327793.ch5openalex-snapshot
Herbicides That Inhibit Photosynthesis
inferred← citeshttps://doi.org/10.1002/9783527655908.ch11openalex-snapshot
The Determination of Abraham Descriptors and Their Application to Crop Protection Research
inferred← citeshttps://doi.org/10.1002/adsc.200600298openalex-snapshot
Synthesis of Indolizines and Benzoindolizines by Annulation of Donor‐Acceptor Cyclopropanes with Electron‐Deficient Pyridines and Quinolines
inferred← citeshttps://doi.org/10.1002/adsc.202300634openalex-snapshot
Cu(II)‐Catalyzed [3+2]‐Annulation of 2‐Pyridinyl‐substituted p ‐Quinone Methides with Enaminones: Access to Functionalized Indolizine Derivatives
inferred← citeshttps://doi.org/10.1002/ajoc.202300202openalex-snapshot
Acetic Acid‐Catalyzed 1,6‐Addition of Indolizine to para‐Quinone Methides
inferred← citeshttps://doi.org/10.1002/ejoc.201900608openalex-snapshot
C‐H Activation/Metalation Approaches for the Synthesis of Indolizine Derivatives
inferred← citeshttps://doi.org/10.1002/jhet.4184openalex-snapshot
AgI ‐promoted one‐pot synthesis of aminoindolizines via sequential Mannich‐Grignard addition and intramolecular cyclization in water
inferred← citeshttps://doi.org/10.1002/ps.3699openalex-snapshot
Mechanisms of resistance to paraquat in plants
inferred← citeshttps://doi.org/10.1002/ps.70394openalex-snapshot
Novel pyridinium salt derivatives as potential inhibitors for photosystem I
inferred← citeshttps://doi.org/10.1007/s00044-014-0940-1openalex-snapshot
Indolizine: a biologically active moiety
inferred← citeshttps://doi.org/10.1007/s00894-017-3328-6openalex-snapshot
A DFT study on the mechanism of the organocatalytic synthesis of a benzoxazine-substituted indolizine derivative
inferred← citeshttps://doi.org/10.1007/s11030-013-9466-6openalex-snapshot
The discovery of 3-(1-aminoethylidene)quinoline-2, 4(1H,3H)-dione derivatives as novel PSII electron transport inhibitors
inferred← citeshttps://doi.org/10.1007/s11030-024-10994-7openalex-snapshot
Larvicidal activity, molecular docking, and molecular dynamics studies of 7-(trifluoromethyl)indolizine derivatives against Anopheles arabiensis
inferred← citeshttps://doi.org/10.1007/s11030-025-11441-xopenalex-snapshot
One-pot synthesis and biological evaluation of substituted 7-chloroindolizines as antimicrobial, antioxidant, and anti-inflammatory agents
inferred← citeshttps://doi.org/10.1016/b978-0-12-822895-1.00006-0openalex-snapshot
Microwave-assisted synthesis of N-heterocycles
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.10.030openalex-snapshot
The role of molecular modeling in the design of analogues of the fungicidal natural products crocacins A and D
inferred← citeshttps://doi.org/10.1016/j.bmc.2009.02.061openalex-snapshot
Beyond physical properties—Application of Abraham descriptors and LFER analysis in agrochemical research
inferred← citeshttps://doi.org/10.1016/j.bmcl.2007.06.076openalex-snapshot
Synthesis and SAR studies of novel antifungal 1,2,3-triazines
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.03.106openalex-snapshot
Novel diamide insecticides: Sulfoximines, sulfonimidamides and other new sulfonimidoyl derivatives
inferred← citeshttps://doi.org/10.1016/j.cdc.2025.101190openalex-snapshot
Synthesis and Biological Evaluation of 1,3,4-oxadiazole ring incorporated (pyrimidin-5-yl)indolizine as Anticancer Agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2011.08.042openalex-snapshot
Recent progress in synthesis and bioactivity studies of indolizines
inferred← citeshttps://doi.org/10.1016/j.molstruc.2017.11.131openalex-snapshot
One-pot microwave assisted synthesis and structural elucidation of novel ethyl 3-substituted-7-methylindolizine-1-carboxylates with larvicidal activity against Anopheles arabiensis
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.138080openalex-snapshot
Crystal structure, hydrogen bonding interactions, Hirshfeld surfaces, energy frameworks, and DFT calculation of Diethyl 3-(4-substitutedbenzoyl)indolizine-1,2-dicarboxylates
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.138980openalex-snapshot
Synthesis of novel π-extended 2,5-disubstituted indolizines and their absorption and fluorescence properties
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.142919openalex-snapshot
Larvicidal activity, molecular docking, and structural analysis of methoxyindolizine-1-carboxylate derivatives
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.142935openalex-snapshot
Design, synthesis, characterization, and larvicidal activity of novel ethyl 3-benzoyl-7-(4-substituted)-indolizine-1-carboxylate and diethyl 3-(4-substituted)-7-(4-nitrobenzyl) indolizine-1,2-dicarboxylate analogs against
inferred← citeshttps://doi.org/10.1016/j.pharep.2018.11.004openalex-snapshot
Novel indolizine derivatives lowers blood glucose levels in streptozotocin-induced diabetic rats: A histopathological approach
inferred← citeshttps://doi.org/10.1016/j.rechem.2024.101451openalex-snapshot
New indazole-indolizine-triazine hybrid molecules with farnesyltransferase inhibitory activity
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134709openalex-snapshot
Design, synthesis, in silico ADME, toxicity prediction, molecular docking studies of 1,2,4-oxadiazole incorporated indolizine-thiadiazole derivatives and their biological evaluation as anticancer agents
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.07.113openalex-snapshot
CuCl catalyzed green and efficient one-pot synthesis of aminoindolizine frameworks via three-component reactions of aldehydes, secondary amines, and terminal alkynes in PEG
inferred← citeshttps://doi.org/10.1021/acs.joc.0c03041openalex-snapshot
[3 + 2]-Annulation of gem-Difluoroalkenes and Pyridinium Ylides: Access to Functionalized 2-Fluoroindolizines
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00114openalex-snapshot
Regiodivergent Synthesis of Densely Functionalized Indolizines via (2 + 2 + 1) Cycloaddition
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01006openalex-snapshot
Domino Approach to Heterocycles-Based Unsymmetrical Triarylmethanes through Heteroannulation of 2-(2-Enynyl)-pyridines with Enaminones
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01203openalex-snapshot
Indolizinylalanine Regioisomers: Tryptophan Isosteres with Bathochromic Fluorescence Emission
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00309openalex-snapshot
Metal-Free Cascade Approach toward Polysubstituted Indolizines from Chromone-Based Michael Acceptors
inferred← citeshttps://doi.org/10.1021/jo702564yopenalex-snapshot
Stereoselective Synthesis of Novel Uracil Polyoxin C Conjugates as Substrate Analogues of Chitin Synthase
inferred← citeshttps://doi.org/10.1039/c7nj05010kopenalex-snapshot
Efficient synthesis and characterization of novel indolizines: exploration of in vitro COX-2 inhibitory activity and molecular modelling studies
inferred← citeshttps://doi.org/10.1039/c9nj05738bopenalex-snapshot
A [bmim]Cl-promoted domino protocol using an isocyanide-based [4+1]-cycloaddition reaction for the synthesis of diversely functionalized 3-alkylamino-2-alkyl/aryl/hetero-aryl indolizine-1-carbonitriles under solvent-free conditions
inferred← citeshttps://doi.org/10.1039/d2cc04395eopenalex-snapshot
Pd( ii )-catalyzed annulation of terminal alkynes with 2-pyridinyl-substituted p -quinone methides: direct access to indolizines
inferred← citeshttps://doi.org/10.1080/00397911.2022.2081811openalex-snapshot
Clean and efficient synthesis of 3-aminoindolizines in one-pot using recyclable CuCN/[bmim]PF 6 system
inferred← citeshttps://doi.org/10.1080/07391102.2017.1345325openalex-snapshot
Molecular modeling studies and anti-TB activity of trisubstituted indolizine analogues; molecular docking and dynamic inputs
inferred← citeshttps://doi.org/10.1134/s1070428020010212openalex-snapshot
Facile Synthesis of 2-Aminocyclobutenylphosphonates
inferred← citeshttps://doi.org/10.1155/2023/1972034openalex-snapshot
Validation of the Non-Motor Symptoms Scale for Parkinson’s Disease of Persian Version
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Computational, crystallographic studies, cytotoxicity and anti-tubercular activity of substituted 7-methoxy-indolizine analogues
inferred← citeshttps://doi.org/10.2139/ssrn.5437713openalex-snapshot
One-Pot Synthesis and Biological Evaluation of Substituted 7-Chloroindolizines as Antimicrobial, Antioxidant, and Anti-Inflammatory Agents
inferred← citeshttps://doi.org/10.2174/2213346110666230120154516openalex-snapshot
Green Synthetic Approach: A Well-organized Eco-friendly Tool for Synthesis of Bio-active Fused Heterocyclic Compounds
inferred← citeshttps://doi.org/10.25236/fmsr.2022.040905openalex-snapshot
Design, synthesis and study of novel indoxine derivatives
inferred← citeshttps://doi.org/10.3390/antibiotics8040247openalex-snapshot
Anti-Tubercular Activity of Substituted 7-Methyl and 7-Formylindolizines and In Silico Study for Prospective Molecular Target Identification
inferred← citeshttps://doi.org/10.3390/molecules26123550openalex-snapshot
Crystallography, Molecular Modeling, and COX-2 Inhibition Studies on Indolizine Derivatives
inferred← citeshttps://doi.org/10.4028/www.scientific.net/amr.781-784.1089openalex-snapshot
Synthesis and Interleukin-6 Inhibitory Activities of 3-Alkyloxylindolizine Derivatives
inferred← citeshttps://doi.org/10.4236/jbm.2025.138012openalex-snapshot
A Promising TNF-α Inhibition Activity of 2-Aminocyclopentenylphosphonates
inferred← citeshttps://doi.org/10.5530/ijper.53.3.87openalex-snapshot
Anti-tubercular Potency and Computationallyassessed Drug-likeness and Toxicology of Diversely Substituted Indolizines
inferred← citeshttps://doi.org/10.70675/c6bb97b1zad41z4960z90cfz40e80fa7b29copenalex-snapshot
Identification et développement chimique d'inducteurs de protéines immunorégulatrices (SLPI et IL-10) à visée thérapeutique
inferred← citeshttps://doi.org/10.71267/mencom.8160openalex-snapshot
Synthesis of indolizines via the A3-coupling reaction catalyzed by Cu-Salphen-Zr metal-organic framework
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Qualitative anti-tubercular activity of synthetic ethyl 7-acetyl- 2-substituted-3-(4-substituted benzoyl) indolizine-1-carboxylate analogues
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