Artículos de revistas sobre el tema "Thio semicarbazides"
Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros
Consulte los 39 mejores artículos de revistas para su investigación sobre el tema "Thio semicarbazides".
Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.
También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.
Explore artículos de revistas sobre una amplia variedad de disciplinas y organice su bibliografía correctamente.
Chen, Wen-Bin y Gui-Yu Jin. "Synthesis ofn-(thio)phosphoryl-n?-2-benzoxazolyl semicarbazides". Heteroatom Chemistry 12, n.º 3 (2001): 151–55. http://dx.doi.org/10.1002/hc.1024.
Texto completoHemdan, Magdy M. "Addition–cyclisation of 3-(2-thienyl)acryloyl isothiocyanate with hydrazine derivatives as a source of triazoles and thiadiazoles". Journal of Chemical Research 2009, n.º 8 (agosto de 2009): 489–91. http://dx.doi.org/10.3184/030823409x12474221035136.
Texto completoChen, Wen-Bin y Gui-Yu Jin. "ChemInform Abstract: Synthesis of N-(Thio)phosphoryl-N′-2-benzoxazolyl Semicarbazides." ChemInform 32, n.º 32 (25 de mayo de 2010): no. http://dx.doi.org/10.1002/chin.200132175.
Texto completoYogeeswari, P., D. Sriram, V. Saraswat, J. Vaigunda Ragavendran, M. Mohan Kumar, S. Murugesan, R. Thirumurugan y J. P. Stables. "Synthesis and anticonvulsant and neurotoxicity evaluation of N4-phthalimido phenyl (thio) semicarbazides". European Journal of Pharmaceutical Sciences 20, n.º 3 (noviembre de 2003): 341–46. http://dx.doi.org/10.1016/j.ejps.2003.08.002.
Texto completoWujec, Monika, Ewa Kędzierska, Edyta Kuśmierz, Tomasz Plech, Andrzej Wróbel, Agata Paneth, Jolanta Orzelska, Sylwia Fidecka y Piotr Paneth. "Pharmacological and Structure-Activity Relationship Evaluation of 4-aryl-1-Diphenylacetyl(thio)semicarbazides". Molecules 19, n.º 4 (16 de abril de 2014): 4745–59. http://dx.doi.org/10.3390/molecules19044745.
Texto completoAlshammari, Mohammed B., Ashraf A. Aly, Stefan Bräse, Martin Nieger y Lamiaa E. Abd El-Haleem. "Efficient Synthesis of Various Substituted (Thio)Ureas, Semicarbazides, Thiosemicarbazides, Thiazolidones, and Oxadiazole Derived from [2.2]Paracyclophane". ACS Omega 7, n.º 15 (6 de abril de 2022): 12879–90. http://dx.doi.org/10.1021/acsomega.2c00141.
Texto completoAwad, Ibrahim M. A., Abdu E. Abdel-Rahman y Etify A. Bakhite. "Synthesis and application of some new S-(substituted)thio- and thienoquinoline derivatives as antimicrobial agents". Collection of Czechoslovak Chemical Communications 56, n.º 8 (1991): 1749–60. http://dx.doi.org/10.1135/cccc19911749.
Texto completoAksenov, Nicolai A., Nikolai A. Arutiunov, Nikita K. Kirillov, Dmitrii A. Aksenov, Alexander V. Aksenov y Michael Rubin. "Preparation of 1,3,4-oxadiazoles and 1,3,4-thiadiazoles via chemoselective сyclocondensation of electrophilically activated nitroalkanes to (thio)semicarbazides or thiohydrazides". Chemistry of Heterocyclic Compounds 56, n.º 8 (agosto de 2020): 1067–72. http://dx.doi.org/10.1007/s10593-020-02775-5.
Texto completoEldehna, Wagdy M., Hadia Almahli, Tamer M. Ibrahim, Mohamed Fares, Tarfah Al-Warhi, Frank M. Boeckler, Adnan A. Bekhit y Hatem A. Abdel-Aziz. "Synthesis, in vitro biological evaluation and in silico studies of certain arylnicotinic acids conjugated with aryl (thio)semicarbazides as a novel class of anti-leishmanial agents". European Journal of Medicinal Chemistry 179 (octubre de 2019): 335–46. http://dx.doi.org/10.1016/j.ejmech.2019.06.051.
Texto completoFernandes, Tiago A., Vânia André, Aliaksandr S. Arol, Ângela França, Sergei Mikhalyonok, Nuno Cerca y Alexander M. Kirillov. "New silver (thio)semicarbazide derivatives: synthesis, structural features, and antimicrobial activity". New Journal of Chemistry 44, n.º 26 (2020): 10924–32. http://dx.doi.org/10.1039/d0nj02013c.
Texto completoLohar, Sisir, Sougata Sinha, Subrata Ghosh y Debasis Das. "Tri-color emission and colorimetric recognition of acetate using semicarbazide and thio-semicarbazide derivatives: Experimental and computational studies". Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 155 (febrero de 2016): 75–80. http://dx.doi.org/10.1016/j.saa.2015.10.018.
Texto completoUzbekov, Marat G. "Pathogenetic Mechanisms of Mental Disorders: Endogenous Intoxication". Biochemistry (Moscow) 88, n.º 4 (abril de 2023): 491–501. http://dx.doi.org/10.1134/s0006297923040053.
Texto completoMalhotra, Rajesh. "Novel Bioactive Thio- and Semicarbazide Ligands and Their Organosilicon (IV) Complexes". Phosphorus, Sulfur, and Silicon and the Related Elements 185, n.º 9 (25 de agosto de 2010): 1875–85. http://dx.doi.org/10.1080/10426500903348021.
Texto completoAljamali, Nagham Mahmood, Nour Abd Alrazzak Abd Allattif y Sabreen Ali Abdalrahman. "Cyclization of Multi Components Reactions and (Preparation, Investigation, Thermal Curves)". American International Journal of Multidisciplinary Scientific Research 2, n.º 1 (10 de octubre de 2018): 1–12. http://dx.doi.org/10.46281/aijmsr.v2i1.190.
Texto completoAllahverdiyeva, G. E., V. M. Ismailov, I. A. Mamedov y N. N. Yusubov. "Reactions of triethyl phosphonoacetate, bromoacetaldehyde diethyl acetal, and (diethoxyphosphoryl)acetaldehyde with thiourea and (thio)semicarbazide". Журнал общей химии 93, n.º 5 (15 de mayo de 2023): 711–16. http://dx.doi.org/10.31857/s0044460x23050062.
Texto completoSong, Gaopeng, Jianzuo Li, Hao Tian, Yasheng Li, Dekun Hu, Ying Li y Zining Cui. "Synthesis and Antitumor Activity of Novel N-Benzoyl-N'-substituted Pyrimidinyl (Thio)semicarbazide Derivatives". Letters in Drug Design & Discovery 13, n.º 4 (3 de marzo de 2016): 329–34. http://dx.doi.org/10.2174/1570180812666151003002644.
Texto completoLiang, Zhaochang, Yuping Huang, Shiben Wang y Xianqing Deng. "Synthesis and Biological Evaluation of Some Pyrazole Derivatives, Containing (Thio) Semicarbazide, as Dual Anti-Inflammatory Antimicrobial Agents". Letters in Drug Design & Discovery 16, n.º 9 (11 de septiembre de 2019): 1020–30. http://dx.doi.org/10.2174/1570180816666190325163117.
Texto completoAllahverdiyeva, G. E., V. M. Ismailov, I. A. Mamedov y N. N. Yusubov. "Reactions of Triethyl Phosphonoacetate, Bromoacetaldehyde Diethyl Acetal, and (Diethoxyphosphoryl)acetaldehyde with Thiourea and (Thio)semicarbazide". Russian Journal of General Chemistry 93, n.º 5 (mayo de 2023): 1064–68. http://dx.doi.org/10.1134/s1070363223050067.
Texto completoLi, Shaoyuan, Wenhui Ma, Xiuhua Chen, Cong Zhang, Xiao He, Yudong Shang, Yuxin Zou y Zhengjie Chen. "Fabrication of an Innovative Lead-Ions Sensitive Electrode Based on Thio-semicarbazide Derivative Modified Nanoporous Silicon". Current Environmental Engineering 3, n.º 3 (20 de diciembre de 2016): 267–72. http://dx.doi.org/10.2174/2212717803666160725152731.
Texto completoJeyashri, K. R., Y. Baby, E. Dhineshkumar, M. Seenivasan y H. Manikandan. "Synthesis, spectral and theoretical studies of some 3-benzylidene amino-1,2,3-triarylpropan-1-one thio/semicarbazide". Materials Today: Proceedings 51 (2022): 2300–2308. http://dx.doi.org/10.1016/j.matpr.2021.11.408.
Texto completoHajalsiddig, Tawassl Tajelsir Hassan y Ahmed Elsadig Mohammed Saeed. "Synthesis of new 6-substituent 2-phenyl and 2-(furan-2-yl)-3-phenyl-quinoline-4-carboxylic acid derivatives". European Journal of Chemistry 10, n.º 1 (31 de marzo de 2019): 57–63. http://dx.doi.org/10.5155/eurjchem.10.1.57-63.1816.
Texto completoTumosienė, Ingrida, Kristina Kantminienė, Arnas Klevinskas, Vilma Petrikaitė, Ilona Jonuškienė y Vytautas Mickevičius. "Antioxidant and Anticancer Activity of Novel Derivatives of 3-[(4-Methoxyphenyl)amino]propanehydrazide". Molecules 25, n.º 13 (29 de junio de 2020): 2980. http://dx.doi.org/10.3390/molecules25132980.
Texto completoXu, Yan, Ran Dang, Jianguo Guan, Zhi Xu, Shijia Zhao y Yuanqiang Hu. "Isatin-(thio)semicarbazide/oxime-1H -1,2,3-triazole-coumarin Hybrids: Design, Synthesis, and in vitro Anti-mycobacterial Evaluation". Journal of Heterocyclic Chemistry 55, n.º 4 (12 de febrero de 2018): 1069–73. http://dx.doi.org/10.1002/jhet.3104.
Texto completoXu, Zhi, Xufeng Song, Yuanqiang Hu, Min Qiang y Zaosheng Lv. "Design, Synthesis andIn VitroAnti-mycobacterial Activities of 8-OMe Ciprofloxacin-1H-1,2,3-triazole-isatin-(thio) Semicarbazide/Oxime Hybrids". Journal of Heterocyclic Chemistry 55, n.º 1 (4 de octubre de 2017): 192–98. http://dx.doi.org/10.1002/jhet.3024.
Texto completoJournal, Baghdad Science. "Synthesis and Characterization of 1,3,4-Oxadiazoles Derived From 9-Fluorenone". Baghdad Science Journal 10, n.º 2 (2 de junio de 2013): 449–61. http://dx.doi.org/10.21123/bsj.10.2.449-461.
Texto completoDawood, Rafid Saad. "Synthesis and Characterization of 1,3,4-Oxadiazoles Derived From 9-Fluorenone". Baghdad Science Journal 10, n.º 2 (2 de junio de 2013): 449–61. http://dx.doi.org/10.21123/bsj.2013.10.2.449-461.
Texto completoKrátký, Martin, Šárka Štěpánková, Klára Konečná, Katarína Svrčková, Jana Maixnerová, Markéta Švarcová, Ondřej Janďourek, František Trejtnar y Jarmila Vinšová. "Novel Aminoguanidine Hydrazone Analogues: From Potential Antimicrobial Agents to Potent Cholinesterase Inhibitors". Pharmaceuticals 14, n.º 12 (26 de noviembre de 2021): 1229. http://dx.doi.org/10.3390/ph14121229.
Texto completoSilva, Bianca N. M., Policarpo A. Sales Junior, Alvaro J. Romanha, Silvane M. F. Murta, Camilo H. S. Lima, Magaly G. Albuquerque, Eliane D'Elia et al. "Synthesis of New Thiosemicarbazones and Semicarbazones Containing the 1,2,3-1H-triazole-isatin Scaffold: Trypanocidal, Cytotoxicity, Electrochemical Assays, and Molecular Docking". Medicinal Chemistry 15, n.º 3 (12 de abril de 2019): 240–56. http://dx.doi.org/10.2174/1573406414666180912120502.
Texto completoKalinina, V., Y. Gryzunov, N. Smolina, M. Uzbekov, E. Misionzhnik y G. Dobretsov. "Disturbance of neurotransmitters monoamines and indices of reducing-oxidizing processes in patient with the first episode of schizophrenia (FES)". European Psychiatry 26, S2 (marzo de 2011): 1412. http://dx.doi.org/10.1016/s0924-9338(11)73117-0.
Texto completoBhandarkar, Subodh y Bhavana Khobragade. "Synthesis and Biological Study of 2-( 5-aryl-4,5-dihydro-1-substituted-pyrazol-3-yl )-Substituted-Naphthalene-1-Ol". Advanced Materials Research 1110 (junio de 2015): 306–10. http://dx.doi.org/10.4028/www.scientific.net/amr.1110.306.
Texto completoPROKOF'EVA, A. F., ZH Z. SAPOZHNIKOVA, L. A. POKROVSKAYA, V. N. VOLKOVA, V. V. NEGREBETSKII, G. V. GOLOVKIN y N. N. MEL'NIKOV. "ChemInform Abstract: Phosphorus-Containing Triazinylhydrazines and Triazinyl(thio)semicarbazides. Synthesis and Properties." ChemInform 20, n.º 24 (13 de junio de 1989). http://dx.doi.org/10.1002/chin.198924218.
Texto completo"Synthesis and Evaluation of Antimicrobial Activities of New Functional Derivatives of 3-[5-(4-Nitrophenyl)-2-Furyl]-4-Pyrazole-Carbaldehydes". Biointerface Research in Applied Chemistry 11, n.º 4 (2 de enero de 2021): 12159–69. http://dx.doi.org/10.33263/briac114.1215912169.
Texto completoPanja, Anangamohan, Mainak Das, Narayan Ch Jana, Paula Brandão, Rosa Maria Gomila, Joaquin Ortega-Castro, Antonio Frontera y Partha Pratim Ray. "Combined experimental and theoretical studies on a conformationally diverse (thio)semicarbazone based semiconducting materials". CrystEngComm, 2023. http://dx.doi.org/10.1039/d3ce00137g.
Texto completoGultekin, Ergün, Olcay Bekircan, Yakup Kolcuoğlu y Atilla Akdemir. "Synthesis of new 1,2,4‐triazole–(thio)semicarbazide hybrid molecules: Their tyrosinase inhibitor activities and molecular docking analysis". Archiv der Pharmazie, 26 de abril de 2021. http://dx.doi.org/10.1002/ardp.202100058.
Texto completode Mello, Debora, Juliana Malavolta, Roberto Santos, Leonardo Lopes, Sidnei Moura, Darlene Flores y Alex Flores. "Efficient Synthesis and Antimicrobial Activities of Long Alkyl Chain Trifluoromethyl1H-pyrazol-1-(thio)carboxamides and Trifluoromethyl-1H-pyrazol-1-yl-thiazoles". Journal of the Brazilian Chemical Society, 2021. http://dx.doi.org/10.21577/0103-5053.20200241.
Texto completo"THE UTILITY OF 1-CYANOACETYL-4-(4-ETHOXYPHENYL) THIO-SEMICARBAZIDE FOR SYNTHESIS OF PYRAZOLE, TRIAZOLE, THIAZOLE, PYRIDINE AND CHROMENE DERIVATIVES". Al-Azhar Bulletin of Science 22, Issue 1-A (1 de junio de 2011): 85–97. http://dx.doi.org/10.21608/absb.2011.7179.
Texto completoAl-Majidi, Suaad, M. H., Halah, A. R. Ibrahim y Yasser, A. H. AL-issa. "Synthesis and Identification of Some New Derivatives of ([Benzyl Thio) Benzimidazole -N- (Methylene-5-Yl)] - 4,5- Di Substituted 1,2,4-Triazole and Evaluation of Their Activity as Antimicrobial and Anti-Inflammatory Agents". Iraqi Journal of Science, 29 de abril de 2021, 1054–65. http://dx.doi.org/10.24996/ijs.2021.62.4.2.
Texto completoHady, Ahmad Ayad, Mayada F. Darweesh y Ahmad A. Motar. "The Antibacterial of Essential Fatty Acid Semicarbazide Extracted from Flaxseed Oil Against Some Nosocomial Infection Bacteria in Iraq". International Journal of Current Pharmaceutical Review and Research 8, n.º 01 (25 de febrero de 2017). http://dx.doi.org/10.25258/ijcprr.v8i01.9086.
Texto completoJyothi, P., V. Sumalatha y D. Rajitha. "Cobalt (II) complexes with N-methyl thio semicarbazide Schiff bases: Synthesis, Spectroscopic investigation, Cytotoxicity, DNA binding and incision, anti-bacterial and anti-fungal studies". Inorganic Chemistry Communications, septiembre de 2022, 110029. http://dx.doi.org/10.1016/j.inoche.2022.110029.
Texto completo