Works matching DE "ACRIDINIUM compounds"
Results: 19
Acridinium Ester Chemiluminescence: Methyl Substitution on the Acridine Moiety.
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- Journal of Oleo Science, 2021, v. 70, n. 11, p. 1677, doi. 10.5650/jos.ess21186
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Optical characteristics of the colored dissolved organic matter on the East Siberian shelf.
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- Doklady Earth Sciences, 2015, v. 465, n. 2, p. 1293, doi. 10.1134/S1028334X15120120
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Preparation of an Acridinium Ester-Labeled Antibody and Its Application in GoldMag Nanoparticle-Based, Ultrasensitive Chemiluminescence Immunoassay for the Detection of Human Epididymis Protein 4.
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- Micromachines, 2017, v. 8, n. 5, p. 149, doi. 10.3390/mi8050149
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Study of the synthesis of novel trisubstituted acridines.
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- ARKIVOC: Online Journal of Organic Chemistry, 2015, v. 2015, p. 134, doi. 10.3998/ark.5550190.p009.033
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Electrochemiluminescence of Acridines.
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- Electroanalysis, 2016, v. 28, n. 11, p. 2672, doi. 10.1002/elan.201600209
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Lattice energetics and thermochemistry of acridine derivatives and substituted acridinium trifluoromethanesulphonates.
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- Journal of Thermal Analysis & Calorimetry, 2017, v. 129, n. 3, p. 1613, doi. 10.1007/s10973-017-6306-4
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The synthesis of dialkylaminonitrile derivatives of 2-formylbenzoic acid by the Strecker reaction in an aqueous medium.
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- Journal of Chemical Research, 2016, v. 40, n. 6, p. 371, doi. 10.3184/174751916X14636641348012
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Design, Synthesis and Antibacterial Activity Evaluation of 9-phenyl-10-(2-phenylalkyl) acridinium bromide: A Novel Acridine Based Antibacterial Agent.
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- Current Trends in Biotechnology & Pharmacy, 2014, v. 8, n. 2, p. 114
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Natural Compounds from Herbs that can Potentially Execute as Autophagy Inducers for Cancer Therapy.
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- International Journal of Molecular Sciences, 2017, v. 18, n. 7, p. 1412, doi. 10.3390/ijms18071412
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Phenolic Esters of O-Desmethylvenlafaxine with Improved Oral Bioavailability and Brain Uptake.
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- Molecules, 2013, v. 18, n. 12, p. 14920, doi. 10.3390/molecules181214920
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OxymaPure/DIC: An Efficient Reagent for the Synthesis of a Novel Series of 4-[2-(2-Acetylaminophenyl)-2-oxo-acetylamino] Benzoyl Amino Acid Ester Derivatives.
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- Molecules, 2013, v. 18, n. 12, p. 14747, doi. 10.3390/molecules181214747
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Novel Oxidative Ugi Reaction for the Synthesis of Highly Active, Visible‐Light, Imide‐Acridinium Organophotocatalysts.
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- Chemistry - A European Journal, 2018, v. 24, n. 48, p. 12509, doi. 10.1002/chem.201802830
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Synthesis of Novel Imidazo[1,2- a]pyridin-2-amines from Arylamines and Nitriles via Sequential Addition and I<sub>2</sub>/KI-Mediated Oxidative Cyclization.
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- Chemistry - A European Journal, 2016, v. 22, n. 22, p. 7617, doi. 10.1002/chem.201600849
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Stereoselective Synthesis of 2‐Deoxyglycosides from Glycals by Visible‐Light‐Induced Photoacid Catalysis.
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- Angewandte Chemie, 2018, v. 130, n. 21, p. 6228, doi. 10.1002/ange.201800909
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Frustrated Lewis Pair Mediated 1,2-Hydrocarbation of Alkynes.
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- Angewandte Chemie, 2017, v. 129, n. 31, p. 9330, doi. 10.1002/ange.201705100
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Oxygenation and chlorination of aromatic hydrocarbons with hydrochloric acid photosensitized by 9-mesityl-10-methylacridinium under visible light irradiation.
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- Research on Chemical Intermediates, 2013, v. 39, n. 1, p. 205, doi. 10.1007/s11164-012-0643-5
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Crystal and Molecular Structures of Four Organic Acid-Base Adducts from Hexamethylenetetramine, N, N, N, N-Tetramethylethylenediamine, and Organic Acids.
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- Journal of Chemical Crystallography, 2016, v. 46, n. 4, p. 188, doi. 10.1007/s10870-016-0647-x
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Measurements of chlorinated volatile organic compounds emitted from office printers and photocopiers.
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- Environmental Science & Pollution Research, 2015, v. 22, n. 7, p. 5241, doi. 10.1007/s11356-014-3672-3
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A green synthesis of chemiluminescent N-sulfopropyl acridinium esters in ionic liquids without using the carcinogen 1,3-propane sultone.
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- Green Chemistry Letters & Reviews, 2013, v. 6, n. 3, p. 237, doi. 10.1080/17518253.2013.768708
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