At the dated check, the references listed below either did not resolve in
Crossref or DataCite, or carried a retraction notice. Each one is shown with the
registry record that put it there.
The 44 checked references that resolve
resolves10.1346/CCMN.2010.0580204Density Functional Theory (DFT) Study of the Hydration Steps of Na<sup>+</sup>/Mg<sup>2+</sup>/Ca<sup>2+</sup>/Sr<sup>2+</sup>/Ba<sup>2+</sup>-Exchanged Montmorillonites
resolves10.1007/s11244-015-0500-zConceptual Process Design and Techno-Economic Assessment of Ex Situ Catalytic Fast Pyrolysis of Biomass: A Fixed Bed Reactor Implementation Scenario for Future Feasibility
resolves10.15446/ing.investig.v36n1.52855Improvements in the synthesis of zeolites with low Si/Al ratio from Venezuelan sodium silicate for an environmentally friendly process
resolves10.1007/s10854-018-0545-4Nanosecond laser-irradiation assisted the improvement of structural, optical and thermal properties of polyvinyl pyrrolidone/carboxymethyl cellulose blend filled with gold nanoparticles
resolves10.1016/j.jmrt.2019.01.011Different time's Nd:YAG laser-irradiated PVA/Ag nanocomposites: structural, optical, and electrical characterization
resolves10.1007/s12633-018-9890-4Nanosecond Laser Irradiation as New Route for Silver Nanoparticles Precipitation in Glassy Matrix
resolves10.1007/s10904-018-0890-zNanosecond Pulsed Laser Ablation in Liquids as New Route for Preparing Polyvinyl Carbazole/Silver Nanoparticles Composite: Spectroscopic and Thermal Studies
resolves10.1021/jm990946nAntimalarial, Antitrypanosomal, and Antileishmanial Activities and Cytotoxicity of Bis(9-amino-6-chloro-2-methoxyacridines): Influence of the Linker
resolves10.1016/S0020-1693(98)00035-8Intercalator-linked cisplatin: synthesis and antitumor activity of cis-dichloroplatinum(II) complexes connected to acridine and phenylquinolines by one methylene chain
resolves10.1021/jm980687mStructure−Activity Relationships for Substituted Bis(acridine-4-carboxamides): A New Class of Anticancer Agents
resolves10.1039/a701401eSynthesis and laser properties of 9-alkyl-3,3,6,6-tetramethyl-1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione derivatives
resolves10.1016/S0223-5234(02)01374-0Vasorelaxing properties of some phenylacridine type potassium channel openers in isolated rabbit thoracic arteries
resolves10.1016/j.molcata.2006.12.039HClO4–SiO2 and PPA–SiO2 catalyzed efficient one-pot Knoevenagel condensation, Michael addition and cyclo-dehydration of dimedone and aldehydes in acetonitrile, aqueous and solvent free conditions: Scope and limitations
resolves10.1016/j.dyepig.2007.02.001Solvent-free synthesis of aryl-14H-dibenzo[a,j]xanthenes and 1,8-dioxo-octahydro-xanthenes using silica sulfuric acid as catalyst
resolves10.1002/aoc.1488ZrOCl<sub>2</sub>·8H<sub>2</sub>O: a highly efficient catalyst for the synthesis of 1,8‐dioxo‐octahydroxanthene derivatives under solvent‐free conditions
resolves10.1016/S1872-2067(15)61005-1Ultrasound assisted multicomponent reactions: A green method for the synthesis of N-substituted 1,8-dioxo-decahydroacridines using β-cyclodextrin as a supramolecular reusable catalyst in water
resolves10.1002/jhet.5570320139Synthesis and conformational study of acridine derivatives related to 1,4‐dihydropyridines
resolves10.1002/jhet.5570410519One‐Pot synthesis of a novel compound <i>N</i>‐hydroxydecahydroacridine under microwave irradiation
resolves10.1081/SCC-120005427A CONVENIENT SYNTHESIS OF 9-ARYL-3,3,6,6-TETRAMETHYL-1,2,3,4,5,6,7,8,9,10-DECAHYDROACRIDINE-1,8-DIONES UNDER MICROWAVE IRRADIATION WITHOUT SOLVENT
resolves10.1016/j.molcata.2005.11.048Amberlyst-15: An efficient reusable heterogeneous catalyst for the synthesis of 1,8-dioxo-octahydroxanthenes and 1,8-dioxo-decahydroacridines
resolves10.1007/s11051-013-2026-2A highly efficient nano-Fe3O4 encapsulated-silica particles bearing sulfonic acid groups as a solid acid catalyst for synthesis of 1,8-dioxo-octahydroxanthene derivatives
resolves10.1016/j.catcom.2017.03.017An efficient route to 1,8-dioxo-octahydroxanthenes and -decahydroacridines using a sulfated zirconia catalyst
resolves10.1016/j.catcom.2007.09.0231-Methylimidazolium triflouroacetate ([Hmim]TFA): An efficient reusable acidic ionic liquid for the synthesis of 1,8-dioxo-octahydroxanthenes and 1,8-dioxo-decahydroacridines
resolves10.1016/j.jfluchem.2009.02.014Brønsted acidic imidazolium salts containing perfluoroalkyl tails catalyzed one-pot synthesis of 1,8-dioxo-decahydroacridines in water
resolves10.5012/bkcs.2013.34.8.2367Immobilization of L-Lysine on Zeolite 4A as an Organic-Inorganic Composite Basic Catalyst for Synthesis of α,β-Unsaturated Carbonyl Compounds under Mild Conditions
resolves10.1002/aoc.4783V<sub>2</sub>O<sub>5</sub> based quadruple nano‐perovskite as a new catalyst for the synthesis of bis and tetrakis heterocyclic compounds
resolves10.1007/s12633-017-9747-2Evaluation of the Optical and Structural Properties of Constructed Bis-indole Derivatives Using (Sm2O3/SiO2) Catalyst
resolves10.1007/s12633-016-9421-0New Approach for Tetrachlorosilane Promoted One-Pot, Condensation Reaction for Tetrahydrobenzo[a]Xanthene-11-Ones with Docking Validation as Aurora Kinase Inhibitor
resolves10.1186/s40360-018-0196-3A newly developed oxime K203 is the most effective reactivator of tabun-inhibited acetylcholinesterase
resolves10.2174/1570180812666150918191550Flexibility in the Molecular Design of Acetylcholinesterase Reactivators: Probing Representative Conformations by Chemometric Techniques and Docking/QM Calculations
resolves10.1080/07391102.2013.765361Reactivation steps by 2-PAM of tabun-inhibited human acetylcholinesterase: reducing the computational cost in hybrid QM/MM methods
resolves10.1080/07391102.2016.1178173Mechanistic studies of new oximes reactivators of human butyryl cholinesterase inhibited by cyclosarin and sarin
The 10 references without a DOI — listed, not checked
no DOI — not checkedN.Iwasaki M.Kato T.Ogawa M.Hosoi U.S. Patent Application no. 15/520 2017 985.
no DOI — not checkedQ.Li R. D.Partridge U.S. Patent Application No. 14/966 2016 407.
no DOI — not checkede_1_2_5_12_1
no DOI — not checkede_1_2_5_15_1
no DOI — not checkede_1_2_5_30_1
no DOI — not checkede_1_2_5_36_1
no DOI — not checkede_1_2_5_37_1
no DOI — not checkede_1_2_5_47_1
no DOI — not checkedThe Molecular Operating E.; Chemical Computing Group I.; Montreal QC. In. 2016.
no DOI — not checkede_1_2_5_56_1
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