Artykuły w czasopismach na temat „Pyrazolone derivatives”
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Abd-Ella, Aly A., Saoud A. Metwally, Mokhtar A. Abd ul-Malik, Yasser A. El-Ossaily, Fathy M. Abd Elrazek, Safwat A. Aref, Youssra A. Naffea i Shaban A. A. Abdel-Raheem. "A review on recent advances for the synthesis of bioactive pyrazolinone and pyrazolidinedione derivatives". Current Chemistry Letters 11, nr 2 (2022): 157–72. http://dx.doi.org/10.5267/j.ccl.2022.2.004.
Pełny tekst źródłaEdrees, Mastoura M. "Synthesis of 4-hydrazinopyrazolo[3,4-d]pyrimidines and their Reactions with Carbonyl Compounds". Journal of Chemical Research 37, nr 1 (styczeń 2013): 6–10. http://dx.doi.org/10.3184/174751912x13543818811749.
Pełny tekst źródłaGil-Ordóñez, Marta, Camille Aubry, Cristopher Niño, Alicia Maestro i José M. Andrés. "Squaramide-Catalyzed Asymmetric Mannich Reaction between 1,3-Dicarbonyl Compounds and Pyrazolinone Ketimines: A Pathway to Enantioenriched 4-Pyrazolyl- and 4-Isoxazolyl-4-aminopyrazolone Derivatives". Molecules 27, nr 20 (17.10.2022): 6983. http://dx.doi.org/10.3390/molecules27206983.
Pełny tekst źródłaGediz Erturk, Aliye, i Hilal Omerustaoglu. "Synthesis and Cytotoxic Evaluation of Some Substituted 5-Pyrazolones and Their Urea Derivatives". Molecules 25, nr 4 (18.02.2020): 900. http://dx.doi.org/10.3390/molecules25040900.
Pełny tekst źródłaPattan, S. R., P. A. Chavan, R. A. Muluk, S. S. Dengale, S. V. Hiremath, K. D. Pansare, S. S. Vetal i J. S. Pattan. "SYNTHESIS AND BIOLOGICAL EVALUATION OF SOME HETEROCYCLES CONTAINING OXADIAZOLE AND PYRAZOLE RING FOR ANTI-BACTERIAL, ANTI-FUNGAL AND ANTI-TUBERCULAR ACTIVITIES". INDIAN DRUGS 49, nr 03 (28.03.2012): 18–24. http://dx.doi.org/10.53879/id.49.03.p0018.
Pełny tekst źródłaYang, Kai, Xiaoze Bao, Ye Yao, Jingping Qu i Baomin Wang. "Iodine-mediated cross-dehydrogenative coupling of pyrazolones and alkenes". Organic & Biomolecular Chemistry 16, nr 34 (2018): 6275–83. http://dx.doi.org/10.1039/c8ob01645c.
Pełny tekst źródłaBrogden, Rex N. "Pyrazolone Derivatives". Drugs 32, Supplement 4 (1986): 60–70. http://dx.doi.org/10.2165/00003495-198600324-00006.
Pełny tekst źródłaManojkumar, Parameswaran, Thengungal Ravi i Gopalakrishnan Subbuchettiar. "Synthesis of coumarin heterocyclic derivatives with antioxidant activity and in vitro cytotoxic activity against tumour cells". Acta Pharmaceutica 59, nr 2 (1.06.2009): 159–70. http://dx.doi.org/10.2478/v10007-009-0018-7.
Pełny tekst źródłaZhang, Wande, Shah Nawaz, Yue Huang, Wenjing Gong, Xingfu Wei, Jingping Qu i Baomin Wang. "C-4 benzofuranylation of pyrazolones by a metal-free catalyzed indirect heteroarylation strategy". Organic & Biomolecular Chemistry 19, nr 46 (2021): 10215–22. http://dx.doi.org/10.1039/d1ob01920a.
Pełny tekst źródłaBao, Xiaoze, Xingyue Wang, Jin-Miao Tian, Xinyi Ye, Baomin Wang i Hong Wang. "Recent advances in the applications of pyrazolone derivatives in enantioselective synthesis". Organic & Biomolecular Chemistry 20, nr 12 (2022): 2370–86. http://dx.doi.org/10.1039/d1ob02426d.
Pełny tekst źródłaNamera, Dipti L., Khushal M. Kapadiya, Mitesh M. Chhatrola i Umed C. Bhoya. "Microwave Assisted Synthesis of some Novel Sulphonamide Bearing Pyrazolone Core Structure". International Letters of Chemistry, Physics and Astronomy 30 (marzec 2014): 116–26. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.30.116.
Pełny tekst źródłaNamera, Dipti L., Khushal M. Kapadiya, Mitesh M. Chhatrola i Umed C. Bhoya. "Microwave Assisted Synthesis of some Novel Sulphonamide Bearing Pyrazolone Core Structure". International Letters of Chemistry, Physics and Astronomy 30 (12.03.2014): 116–26. http://dx.doi.org/10.56431/p-d7mgbf.
Pełny tekst źródłaGadhave, Anil, Shashikant Kuchekar i Bhausaheb Karale. "Ultrasonication-Induced Synthesis and Antimicrobial Evaluation of Some Multifluorinated Pyrazolone Derivatives". Journal of Chemistry 2013 (2013): 1–9. http://dx.doi.org/10.1155/2013/741953.
Pełny tekst źródłaAbdel Hafez, Ali A. "Synthesis of Some Heterocyclic Sulfones Related to Quinolinol". Collection of Czechoslovak Chemical Communications 58, nr 9 (1993): 2222–26. http://dx.doi.org/10.1135/cccc19932222.
Pełny tekst źródłaZaiter, Jamila, Hanane Achibat, Ouafa Amiri, Abderrafia Hafid, Mostafa Khouili, El Mostapha Rakib, Cláudia M. B. Neves i in. "An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one". New Journal of Chemistry 39, nr 9 (2015): 6738–41. http://dx.doi.org/10.1039/c5nj01306b.
Pełny tekst źródłaEl-Ossaily, Yasser A., Nuha M. M. Alanazi, Ibrahim O. Althobaiti, Hamud A. Altaleb, Nayef S. Al-Muailkel, Mohamed Y. El-Sayed, Modather F. Hussein i in. "Multicomponent approach to the synthesis and spectral characterization of some 3,5-pyrazolididione derivatives and evaluation as anti-inflammatory agents". Current Chemistry Letters 13, nr 1 (2024): 127–40. http://dx.doi.org/10.5267/j.ccl.2023.8.003.
Pełny tekst źródłaYuan, Huijun, Yao Li, Hanhui Zhao, Zhihong Yang, Xin Li i Wenjun Li. "Asymmetric synthesis of atropisomeric pyrazole via an enantioselective reaction of azonaphthalene with pyrazolone". Chemical Communications 55, nr 84 (2019): 12715–18. http://dx.doi.org/10.1039/c9cc06360a.
Pełny tekst źródłaA. Almehizia, Abdulrahman, Ahmad M. Naglah, Amer A. Zen, Tamer K. Khatab i Ashraf S. Hassan. "TCS/ZnCl2 as a controlled reagent for the Michael addition and heterocyclic cyclization based on the phenyl pyrazolone scaffold with docking validation as a Covid-19 protease inhibitor". Bulletin of the Chemical Society of Ethiopia 38, nr 4 (30.04.2024): 1119–27. http://dx.doi.org/10.4314/bcse.v38i4.24.
Pełny tekst źródłaLi, Jun-Hua, i Da-Ming Du. "Enantioselective synthesis of chiral heterocycles containing both chroman and pyrazolone derivatives catalysed by a chiral squaramide". Organic & Biomolecular Chemistry 13, nr 20 (2015): 5636–45. http://dx.doi.org/10.1039/c4ob02653e.
Pełny tekst źródłaHamama, Wafaa S., Mohamed A. Ismail, Hana’a A. Al-Saman i Hanafi H. Zoorob. "Convenient Selective Synthesis of Substituted Pyrido[2,3-d]pyrimidones and Annulated Derivatives". Zeitschrift für Naturforschung B 62, nr 1 (1.01.2007): 104–10. http://dx.doi.org/10.1515/znb-2007-0115.
Pełny tekst źródłaHassan, Alaa A., Yusria R. Ibrahim i Ahmed M. Shawky. "Reactions of Substituted Carbohydrazides with Electron-poor Olefins". Zeitschrift für Naturforschung B 63, nr 8 (1.08.2008): 998–1004. http://dx.doi.org/10.1515/znb-2008-0813.
Pełny tekst źródłaLeleu-Chavain, Natascha, Romain Regnault, Hania Ahouari, Raphaël Le Biannic, Mostafa Kouach, Frédérique Klupsch, Romain Magnez i in. "Antioxidant Properties and Aldehyde Reactivity of PD-L1 Targeted Aryl-Pyrazolone Anticancer Agents". Molecules 27, nr 10 (21.05.2022): 3316. http://dx.doi.org/10.3390/molecules27103316.
Pełny tekst źródłaCho, Joungmo, Venkata Subbaiah Sadu, Yohan Han, Yunsoo Bae, Hwajeong Lee i Kee-In Lee. "Structural Requirements of 1-(2-Pyridinyl)-5-pyrazolones for Disproportionation of Boronic Acids". Molecules 26, nr 22 (11.11.2021): 6814. http://dx.doi.org/10.3390/molecules26226814.
Pełny tekst źródłaMahajan, Suruchi, Pankaj Chauhan, Uğur Kaya, Kristina Deckers, Kari Rissanen i Dieter Enders. "Enantioselective synthesis of pyrazolone α-aminonitrile derivatives via an organocatalytic Strecker reaction". Chemical Communications 53, nr 49 (2017): 6633–36. http://dx.doi.org/10.1039/c7cc02874a.
Pełny tekst źródłaShyshkina, Olena O., Volodymyr V. Medviediev, Oleg V. Shishkin, Andrii I. Kysil i Yulian M. Volovenko. "Unexpected synthesis of pyrazolone derivatives". Tetrahedron 71, nr 8 (luty 2015): 1283–86. http://dx.doi.org/10.1016/j.tet.2014.12.082.
Pełny tekst źródłaAchuthanandhan, Jyothi, i Baskar Lakshmanan. "Docking studies of tetra substituted pyrazolone derivatives as potential antiviral agents". JOURNAL OF PHARMACEUTICAL CHEMISTRY 5, nr 2 (20.12.2018): 5–8. http://dx.doi.org/10.14805/jphchem.2018.art103.
Pełny tekst źródłaParveen, Mehtab, Shaista Azaz, Ali Mohammed Malla, Faheem Ahmad, Musheer Ahmad i Mayank Gupta. "An SiO2/ZnBr2 mediated expeditious approach to 3-methyl-1-phenyl-1H-pyrazol-5(4H)-one derivatives in water under microwave irradiation". RSC Advances 6, nr 1 (2016): 148–62. http://dx.doi.org/10.1039/c5ra21146h.
Pełny tekst źródłaAhmed, Badie, i Jasim Abdullah. "Ultrasound Assisted Synthesis Of Pyrazolone Derivatives". JOURNAL OF EDUCATION AND SCIENCE 26, nr 5 (1.12.2013): 57–63. http://dx.doi.org/10.33899/edusj.2013.163055.
Pełny tekst źródłaPavlov, P. T., A. F. Goleneva, A. E. Lesnov i T. S. Prokhorova. "Biological activity of some pyrazolone derivatives". Pharmaceutical Chemistry Journal 32, nr 7 (lipiec 1998): 370–72. http://dx.doi.org/10.1007/bf02645994.
Pełny tekst źródłaIshihara, Yoshimi, Takeyuki Ito, Hiroshi Saito i Jiro Takano. "Reaction of acridine with pyrazolone derivatives". Journal of Heterocyclic Chemistry 42, nr 5 (lipiec 2005): 963–67. http://dx.doi.org/10.1002/jhet.5570420533.
Pełny tekst źródłaZonouz, Adeleh Moshtaghi, Masoumeh Beiranvand, Rahim Mohammad-Rezaei i Soheila Naderi. "Green and Efficient Synthesis of Fluorescent Bis(pyrazolyl)methanes in Choline Chloride/Urea Deep Eutectic Solvent". Letters in Organic Chemistry 17, nr 7 (7.07.2020): 548–54. http://dx.doi.org/10.2174/1570178617666191111121813.
Pełny tekst źródłaKashinath, Dhurke, Kota Sathish i Sakkani Nagaraju. "Synthesis of Spiro Pyrazolone-Oxindole and Bicyclic Pyrazolone Derivatives via Solvent-Dependent Regioselective Aza-1,4/1,6-Michael and Intramolecular Cycloaddition under Catalyst-Free Conditions". SynOpen 05, nr 02 (13.04.2021): 123–33. http://dx.doi.org/10.1055/a-1480-9837.
Pełny tekst źródłaGuo, Jixi, Yucai Zhang, Dianzeng Jia, Mingxi Guo i Yinhua Li. "Design and synthesis of reversible solid-state photochromic pyrazolones by introducing a pyridine ring". Photochemical & Photobiological Sciences 15, nr 10 (2016): 1222–26. http://dx.doi.org/10.1039/c6pp00119j.
Pełny tekst źródłaWang, Jun, Guan-Cheng Xu, Yan-Ping Zhang, Hua-Ying Luo, Jin-Yao Li, Li Zhang i Dian-Zeng Jia. "Copper(ii) complexes with 4-acyl pyrazolone derivatives and diimine coligands: synthesis, structural characterization, DNA binding and antitumor activity". New Journal of Chemistry 43, nr 6 (2019): 2529–39. http://dx.doi.org/10.1039/c8nj02695e.
Pełny tekst źródłaDeyab, M. A., A. S. Fouda, M. M. Osman i S. Abdel-Fattah. "Mitigation of acid corrosion on carbon steel by novel pyrazolone derivatives". RSC Advances 7, nr 71 (2017): 45232–40. http://dx.doi.org/10.1039/c7ra08761f.
Pełny tekst źródłaAo, Chaoqun, Jingjing Huang, Xinfang Xu, Shikun Jia, Zhenghui Kang i Wenhao Hu. "A Rh-catalyzed three-component reaction for the diastereoselective synthesis of pyrazolone derivatives with contiguous quaternary stereocenters". Organic & Biomolecular Chemistry 18, nr 18 (2020): 3466–70. http://dx.doi.org/10.1039/d0ob00482k.
Pełny tekst źródłaMarzouk, Magda Ismail, Galal Hosni Sayed, Mohamed Said Abd ElHalim i Salma Yehia Mansour. "Synthesis and characterization of novel pyrazolone derivatives". European Journal of Chemistry 5, nr 1 (31.03.2014): 24–32. http://dx.doi.org/10.5155/eurjchem.5.1.24-32.870.
Pełny tekst źródłaRadini, Ibrahim. "Design, Synthesis, and Antimicrobial Evaluation of Novel Pyrazoles and Pyrazolyl 1,3,4-Thiadiazine Derivatives". Molecules 23, nr 9 (21.08.2018): 2092. http://dx.doi.org/10.3390/molecules23092092.
Pełny tekst źródłaDe Crescentini, L., F. R. Perrulli, G. Favi, S. Santeusanio, G. Giorgi, O. A. Attanasi i F. Mantellini. "Reactions of 1,2-diaza-1,3-butadienes with propargyl alcohol as an approach to novel bi-heterocyclic systems". Organic & Biomolecular Chemistry 14, nr 37 (2016): 8674–78. http://dx.doi.org/10.1039/c6ob01595f.
Pełny tekst źródłaLi, Jun-Hua, i Da-Ming Du. "Correction: Enantioselective synthesis of chiral heterocycles containing both chroman and pyrazolone derivatives catalysed by a chiral squaramide". Organic & Biomolecular Chemistry 13, nr 26 (2015): 7337. http://dx.doi.org/10.1039/c5ob90099a.
Pełny tekst źródłaMOHAMMAD, Abeer Essa, Munther Abduljaleel MUHAMMAD-ALI i Ekhlas Qanber JASIM. "SYNTHESIS, DOCKING STUDY, AND BIOLOGICAL EVALUATION OF 4-AMINOANTIPYRINE-ISONIAZID DERIVATIVES AS A HYBRID ANTIBACTERIAL AND ANALGESIC AGENTS". Periódico Tchê Química 19, nr 42 (11.10.2022): 12–28. http://dx.doi.org/10.52571/ptq.v19.n42.2022.02_munther_pgs_12_28.pdf.
Pełny tekst źródłaRegnault, Romain, Frédérique Klupsch, Hassiba El-Bouazzati, Romain Magnez, Raphaël Le Biannic, Natascha Leleu-Chavain, Hania Ahouari i in. "Novel PD-L1-Targeted Phenyl-Pyrazolone Derivatives with Antioxidant Properties". Molecules 28, nr 8 (15.04.2023): 3491. http://dx.doi.org/10.3390/molecules28083491.
Pełny tekst źródłaSun, Bing-Bing, Jun-Bo Chen, Jun-Qi Zhang, Xiao-Peng Yang, Hao-Peng Lv, Zheng Wang i Xing-Wang Wang. "Organo-catalyzed asymmetric cascade annulation reaction for the construction of bi-spirocyclic pyrazolone and oxindole derivatives". Organic Chemistry Frontiers 7, nr 5 (2020): 796–809. http://dx.doi.org/10.1039/d0qo00001a.
Pełny tekst źródłaArora, Kishor. "In-Silico QSAR Studies of Some Pyrazolone Compounds". European Journal of Advanced Chemistry Research 4, nr 4 (18.10.2023): 1–8. http://dx.doi.org/10.24018/ejchem.2023.4.4.148.
Pełny tekst źródłaEl-Mahdy, Kamelia. "Synthesis of Some New Tetracyclic Pyrimidine Derivatives Using Exocyclic α,β-Unsaturated Ketone and Evaluation of Their Antitumor Activities". JOURNAL OF ADVANCES IN CHEMISTRY 12, nr 8 (1.05.2016): 311–17. http://dx.doi.org/10.24297/jac.v12i8.2840.
Pełny tekst źródłaEl-Mahdy, Kamelia. "Synthesis of Some New Tetracyclic Pyrimidine Derivatives Using Exocyclic α,β-Unsaturated Ketone and Evaluation of Their Antitumor Activities". JOURNAL OF ADVANCES IN CHEMISTRY 4, nr 1 (19.04.2008): 311–17. http://dx.doi.org/10.24297/jac.v4i1.960.
Pełny tekst źródłaAshtekar, Harsha, Prarambh S. R. Dwivedi, Natasha Aggarwal, Zeena Fernandes i Nimmy Varghese. "In-silico Validation of Pyrazolone Derivatives as the Potent Scaff old for Modulating Protein Abnormalities Associated with Parkinson’s Disease". INTERNATIONAL JOURNAL OF DRUG DELIVERY TECHNOLOGY 13, nr 01 (25.03.2023): 1–9. http://dx.doi.org/10.25258/ijddt.13.1.01.
Pełny tekst źródłaYoon, Sanghyun, Byunghun Choi, Md Morshedur Rahman, Santosh Kumar, Shekh Md Mamun Kabir i Joonseok Koh. "Dyeing of Polyester with 4-Fluorosulfonylphenylazo-5-pyrazolone Disperse Dyes and Application of Environment-Friendly Aftertreatment for Their High Color Fastness". Materials 12, nr 24 (14.12.2019): 4209. http://dx.doi.org/10.3390/ma12244209.
Pełny tekst źródłaPégurier, Cécile, Philippe Collart, Pierre Danhaive, Sabine Defays, Michel Gillard, Frédéric Gilson, Thierry Kogej i in. "Pyrazolone methylamino piperidine derivatives as novel CCR3 antagonists". Bioorganic & Medicinal Chemistry Letters 17, nr 15 (sierpień 2007): 4228–31. http://dx.doi.org/10.1016/j.bmcl.2007.05.035.
Pełny tekst źródłaWang, Jin-Jun, Bing-Zhu Yin, Gui-Ji Jiang i Kimiaki Imafuku. "Synthesis of isochroman-fused pyrazolone and pyrimidine derivatives". Journal of Heterocyclic Chemistry 27, nr 5 (lipiec 1990): 1181–84. http://dx.doi.org/10.1002/jhet.5570270504.
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