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Fatty Acids in Heterocyclic Synthesis. Part XI: Facile and Convenient Routes to Synthesize Ecofriendly Polyfunctionalized Thiadiazoles, Triazole, Thiadiazolo [3,2-a] pyrimidines and Imidazo[2,1-b]thiadiazole for Pharmaceutical and Industrial Purposes. Egypt. J.Chem., (2013), 56 (5): 379-401.
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Fatty Acids in Heterocyclic Synthesis
Part XII: Synthesis of Surfactants from Pyrazole, Isoxazole, Pyrimidine and Triazine, Incorporating the 1,3,4-Thiadiazole Moiety Having Dyeing and Antimicrobial Activities.
Journal of Surfactants and Detergents, (03/2012), 15(2):179-190.
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Fatty Acids in Heterocyclic Synthesis
Part XIII: 2-Chloro-5-heptadecyl [1,3,4] thiadiazole as a Building Block for Synthesis of s-triazolo [2,4-b] thiadiazole, benzimidiazo [2,1-b] thiadiazole, thiadiazolo [2,3-b] quinazolin-5-one as well as Thiadiazole-2-yl (piperidine, pyridiazine and/or phthalazine).
OLAJ, Szappan Kozmetika, (07/2011), 60(3): 51-58.
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Fatty Acids in Heterocyclic Synthesis.
Part XIV: Synthesis of Surface Active Agents from Some Novel Class of Oxadiazole, Thiadiazole and Triazole Derivatives Having Microbiological Activities. Journal of Surfactants and Detergents, (05/2014), 17(3): 509-523.
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Nucleic Acid Targeted Therapy: G4 Oligonucleotides Downregulate HRAS in Bladder Cancer Cells through a Decoy Mechanism. ACS Med. Chem. Lett., (2015), 6 (12), 1179-1183
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Synthesis of New DNA G-Quadruplex Constructs with Anthraquinone Insertions and Their Anticoagulant Activity, Helv. Chim. Acta, (2016), 99 (2), 116-124.
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Synthesis and Molecular Modeling of Thermally Stable DNA G-Quadruplexes with Anthraquinone Insertions, EurJOC, (2017), 21, 3092-3100.
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Improved i-Motif Thermal Stability by Insertion of
Anthraquinone Monomers, Org. Biomol. Chem., (2017), 15 (31), 6613-6621.
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Novel Assemblies Based on Oligonucleotides Containing Intercalating Nucleic Acid Monomers, Nucleosides, Nucleotides & Nucleic Acids, (2020), 39 (1-3), 82-96.
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Carbazole Modified Oligonucleotides: Synthesis, Hybridization Studies and Fluorescence Properties, Org. Biomol. Chem., (2020), 18 (35), 6935-6948.
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Chemical Modifications and Design Influence the Potency of Huntingtin Anti-Gene Oligonucleotides, (2023), 33 (2), 117-131.
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