Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 32 checked references that resolve
resolves10.1002/anie.201300117Synthesis and Characterization of a Stable, Catenated N<sub>11</sub> Energetic Salt
resolves10.1002/ejic.2013013634‐(1‐Amino‐5‐aminotetrazolyl)methyleneimino‐3‐methylfuroxan and Its Derivatives: Synthesis, Characterization, and Energetic Properties
resolves10.1002/anie.201408127Bis(nitroamino‐1,2,4‐triazolates): <i>N</i>‐Bridging Strategy Toward Insensitive Energetic Materials
resolves10.1002/chem.201402762<i>N</i>‐Diazo‐Bridged Nitroazoles: Catenated Nitrogen‐Atom Chains Compatible with Nitro Functionalities
resolves10.1002/chem.201404991Energetic <i>N</i>,<i>N</i>′‐Ethylene‐Bridged Bis(nitropyrazoles): Diversified Functionalities and Properties
resolves10.1039/c1jm10340g4-Amino-3,5-dinitropyrazolate salts—highly insensitive energetic materials
resolves10.1002/chem.201202483Nitrogen‐Rich Bis‐1,2,4‐triazoles—A Comparative Study of Structural and Energetic Properties
resolves10.1002/chem.201300691The Chemistry of 5‐(Tetrazol‐1‐yl)‐2<i>H</i>‐tetrazole: An Extensive Study of Structural and Energetic Properties
resolves10.1002/asia.201300063Synthesis and Characterization of 5‐(1,2,4‐Triazol‐3‐yl)tetrazoles with Various Energetic Functionalities
resolves10.1002/anie.201412303Energetic Materials with Promising Properties: Synthesis and Characterization of 4,4′‐Bis(5‐nitro‐1,2,3‐2<i>H</i>‐triazole) Derivatives
resolves10.1002/ejic.201200221Insensitive Nitrogen‐Rich Energetic Compounds Based on the 5,5′‐Dinitro‐3,3′‐bi‐1,2,4‐triazol‐2‐ide Anion
resolves10.1021/jo01337a030Synthesis of 3(5)-(1'-pyrazolyl)pyrazoles from 1,4-dinitropyrazole by cine substitution reaction. Structure determination
resolves10.1021/jo00437a024Pyrazoles. 15. Nucleophilic substitution reactions on N-nitropyrazoles
resolves10.1007/s11172-010-0024-4Nitropyrazoles 14. Synthesis of 1,3,4-trinitropyrazole and its behavior in the nucleophilic substitution reactions. General method of synthesis of 5-substituted 3,4-dinitropyrazoles
resolves10.1002/anie.201507456From <i>N</i>‐Nitro to <i>N</i>‐Nitroamino: Preparation of High‐Performance Energetic Materials by Introducing Nitrogen‐Containing Ions
resolves10.1021/ja404164jA Study of Dinitro-bis-1,2,4-triazole-1,1′-diol and Derivatives: Design of High-Performance Insensitive Energetic Materials by the Introduction of N-Oxides
resolves10.1002/chem.201301339A Study of 5‐(1,2,4‐Triazol‐<i>C</i>‐yl)tetrazol‐1‐ols: Combining the Benefits of Different Heterocycles for the Design of Energetic Materials
resolves10.1039/c2ta01359b4-Chloro-3,5-dinitropyrazole: a precursor for promising insensitive energetic compounds
resolves10.1021/tx00020a019Molecular recognition between oligopeptides and nucleic acids: DNA binding selectivity of a series of 1,2,4-triazole-containing lexitropsins
The 4 references without a DOI — listed, not checked
no DOI — not checkedC5TA09803C-(cit7b)/*[position()=1]
no DOI — not checkedhttp://webbook.nist.gov/chemistry/
no DOI — not checkedG. M. Sheldrick , SADABS: Area Detector Absorption Correction , University of Göttingen , Germany , 2001
no DOI — not checkedC5TA09803C-(cit28)/*[position()=1]
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