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Synthesis of mesoionic 3-aryl(hetaryl)-1,2,3,4-oxatriazol-5-ones b based on N-aryl-and N-hetarylhydrazones of bromonitroformaldehyde
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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/ardp.19953280209openalex-snapshot
New NO‐Donors with Antithrombotic and Vasodilating Activities, XII: Mesoionic Oxatriazoles and Related Noncyclic Nitrosohydrazine Derivatives
inferredcites →https://doi.org/10.1002/jhet.5570170501openalex-snapshot
Hydrazidoyl Halides in the Synthesis of Heterocycles
inferredcites →https://doi.org/10.1002/jlac.19535790106openalex-snapshot
Beiträge zur Substituentenwirkung I. Eine Reaktivitätsreihe aktiver Methylenverbindungen
inferredcites →https://doi.org/10.1002/oms.1210131102openalex-snapshot
Chemical ionization of aliphatic nitro compounds
inferredcites →https://doi.org/10.1016/b978-0-12-386011-8.00004-6openalex-snapshot
Advances in Heterocyclic Chemistry
inferredcites →https://doi.org/10.1021/cr00002a004openalex-snapshot
A survey of Hammett substituent constants and resonance and field parameters
inferredcites →https://doi.org/10.1021/ja00320a026openalex-snapshot
Considered stable carbocation. 250. .alpha.-Nitrodiarylmethyl cations
inferredcites →https://doi.org/10.1021/jm00354a023openalex-snapshot
Preliminary studies of mesoionic 3-(substituted-aryl)-.psi.-oxatriazoles as potential antihypertensive agents
inferredcites →https://doi.org/10.1039/p19860001171openalex-snapshot
Bromonitromethane—a versatile electrophile
inferredcites →https://doi.org/10.1070/mc1997v007n02abeh000670openalex-snapshot
Synthesis of 4-diazo-3,5-dinitropyrazole and characteristic features of its behaviour towards nucleophiles
inferredcites →https://doi.org/10.1070/rc1980v049n01abeh002443openalex-snapshot
The Chemistry of Sydnone Imines
inferredcites →https://doi.org/10.1070/rc1997v066n08abeh000317openalex-snapshot
Exogenous nitric oxide donors and inhibitors of its formation (the chemical aspects)
inferredcites →https://doi.org/10.1135/cccc19900728openalex-snapshot
Heterocyclic synthesis from 3-amino-4-cyanopyrazole
inferredcites →https://doi.org/10.1142/9789812791405_0073openalex-snapshot
α-Nitrodiarylmethyl Cations
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.4015280openalex-extracted
Lone Pair/π-Hole Interactions in the Edge-to-Face Stacking of the Criss-Cross Construction Molecule: Towards Thermally Stability, Low Sensitivity, and High Detonation Performance
inferred← citeshttps://doi.org/10.1002/chem.201903526openalex-snapshot
Straightforward Access to the Nitric Oxide Donor Azasydnone Scaffold by Cascade Reactions of Amines
inferred← citeshttps://doi.org/10.1002/chem.202002664openalex-snapshot
Tetrazole Azasydnone (C2N7O2H) And Its Salts: High‐Performing Zwitterionic Energetic Materials Containing A Unique Explosophore
inferred← citeshttps://doi.org/10.1002/chin.200008152openalex-snapshot
ChemInform Abstract: Synthesis of Mesoionic 3‐Aryl(hetaryl)‐1,2,3,4‐oxatriazol‐5‐ones Based on N‐Aryl‐ and N‐Hetarylhydrazones of Bromonitroformaldehyde.
inferred← citeshttps://doi.org/10.1007/s10593-023-03195-xopenalex-snapshot
The reactions of arylazasydnones with S- and O-nucleophiles
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Type A mesoionic compounds (1980–2020)
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Sensitivity of energetic materials: Evidence of thermodynamic factor on a large array of CHNOFCl compounds
inferred← citeshttps://doi.org/10.1016/j.enmf.2020.11.002openalex-snapshot
Azasydnones and their use in Energetic Materials
inferred← citeshttps://doi.org/10.1016/j.enmf.2025.12.005openalex-snapshot
Construction of high energy density azasydnone-pyrazole compounds
inferred← citeshttps://doi.org/10.1016/j.poly.2022.115734openalex-snapshot
Lone pair/π-hole interactions in the edge-to-face stacking of the criss-cross construction molecule: Towards thermally stability, low sensitivity, and high detonation performance
inferred← citeshttps://doi.org/10.1016/j.tca.2017.02.019openalex-snapshot
Thermal decomposition peculiarities and combustion behavior of nitropyrazoles
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.1c00469openalex-snapshot
Heterocyclic Nitrilimines and Their Use in the Synthesis of Complex High-Nitrogen Materials
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02628openalex-snapshot
Nitration of Tricyclic Compound Bis([1,2,4]triazole)[1,5-b:3′,4′-f]pyridazin-8-amine: Mechanistic Insights and Synthetic Exploration
inferred← citeshttps://doi.org/10.1039/c8ta06895jopenalex-snapshot
Azasydnone – novel “green” building block for designing high energetic compounds
inferred← citeshttps://doi.org/10.24820/ark.5550190.p011.203openalex-snapshot
The influence of electronegativity on linear and triangular three-centre bonds
inferred← citeshttps://doi.org/10.3390/molecules26185705openalex-snapshot
Recent Advances in the Synthesis and Biomedical Applications of Heterocyclic NO-Donors
inferred← citeshttps://doi.org/10.70675/61716fdczafbaz4f9fza71dz8e23f5b0bc6dopenalex-snapshot
Synthèse et réactivité de nouvelles azimines, précurseurs de triaziridines pour la propulsion spatiale
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Les mésoioniques : de nouveaux outils pour la chimie bioorthogonale
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Matériaux énergétiques polyazotés : synthèse de l’anion pentazolate par oxydation à l’iode hypervalent et réactivité des azimines en cycloaddition 1,3-dipolaire
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