Статті в журналах з теми "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, and Shaban A. A. Abdel-Raheem. "A review on recent advances for the synthesis of bioactive pyrazolinone and pyrazolidinedione derivatives." Current Chemistry Letters 11, no. 2 (2022): 157–72. http://dx.doi.org/10.5267/j.ccl.2022.2.004.
Повний текст джерелаEdrees, Mastoura M. "Synthesis of 4-hydrazinopyrazolo[3,4-d]pyrimidines and their Reactions with Carbonyl Compounds." Journal of Chemical Research 37, no. 1 (January 2013): 6–10. http://dx.doi.org/10.3184/174751912x13543818811749.
Повний текст джерелаGil-Ordóñez, Marta, Camille Aubry, Cristopher Niño, Alicia Maestro, and 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, no. 20 (October 17, 2022): 6983. http://dx.doi.org/10.3390/molecules27206983.
Повний текст джерелаGediz Erturk, Aliye, and Hilal Omerustaoglu. "Synthesis and Cytotoxic Evaluation of Some Substituted 5-Pyrazolones and Their Urea Derivatives." Molecules 25, no. 4 (February 18, 2020): 900. http://dx.doi.org/10.3390/molecules25040900.
Повний текст джерелаPattan, S. R., P. A. Chavan, R. A. Muluk, S. S. Dengale, S. V. Hiremath, K. D. Pansare, S. S. Vetal, and 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, no. 03 (March 28, 2012): 18–24. http://dx.doi.org/10.53879/id.49.03.p0018.
Повний текст джерелаYang, Kai, Xiaoze Bao, Ye Yao, Jingping Qu, and Baomin Wang. "Iodine-mediated cross-dehydrogenative coupling of pyrazolones and alkenes." Organic & Biomolecular Chemistry 16, no. 34 (2018): 6275–83. http://dx.doi.org/10.1039/c8ob01645c.
Повний текст джерелаBrogden, Rex N. "Pyrazolone Derivatives." Drugs 32, Supplement 4 (1986): 60–70. http://dx.doi.org/10.2165/00003495-198600324-00006.
Повний текст джерелаManojkumar, Parameswaran, Thengungal Ravi, and Gopalakrishnan Subbuchettiar. "Synthesis of coumarin heterocyclic derivatives with antioxidant activity and in vitro cytotoxic activity against tumour cells." Acta Pharmaceutica 59, no. 2 (June 1, 2009): 159–70. http://dx.doi.org/10.2478/v10007-009-0018-7.
Повний текст джерелаZhang, Wande, Shah Nawaz, Yue Huang, Wenjing Gong, Xingfu Wei, Jingping Qu, and Baomin Wang. "C-4 benzofuranylation of pyrazolones by a metal-free catalyzed indirect heteroarylation strategy." Organic & Biomolecular Chemistry 19, no. 46 (2021): 10215–22. http://dx.doi.org/10.1039/d1ob01920a.
Повний текст джерелаBao, Xiaoze, Xingyue Wang, Jin-Miao Tian, Xinyi Ye, Baomin Wang, and Hong Wang. "Recent advances in the applications of pyrazolone derivatives in enantioselective synthesis." Organic & Biomolecular Chemistry 20, no. 12 (2022): 2370–86. http://dx.doi.org/10.1039/d1ob02426d.
Повний текст джерелаNamera, Dipti L., Khushal M. Kapadiya, Mitesh M. Chhatrola, and Umed C. Bhoya. "Microwave Assisted Synthesis of some Novel Sulphonamide Bearing Pyrazolone Core Structure." International Letters of Chemistry, Physics and Astronomy 30 (March 2014): 116–26. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.30.116.
Повний текст джерелаNamera, Dipti L., Khushal M. Kapadiya, Mitesh M. Chhatrola, and Umed C. Bhoya. "Microwave Assisted Synthesis of some Novel Sulphonamide Bearing Pyrazolone Core Structure." International Letters of Chemistry, Physics and Astronomy 30 (March 12, 2014): 116–26. http://dx.doi.org/10.56431/p-d7mgbf.
Повний текст джерелаGadhave, Anil, Shashikant Kuchekar, and 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.
Повний текст джерелаAbdel Hafez, Ali A. "Synthesis of Some Heterocyclic Sulfones Related to Quinolinol." Collection of Czechoslovak Chemical Communications 58, no. 9 (1993): 2222–26. http://dx.doi.org/10.1135/cccc19932222.
Повний текст джерелаZaiter, Jamila, Hanane Achibat, Ouafa Amiri, Abderrafia Hafid, Mostafa Khouili, El Mostapha Rakib, Cláudia M. B. Neves, et al. "An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one." New Journal of Chemistry 39, no. 9 (2015): 6738–41. http://dx.doi.org/10.1039/c5nj01306b.
Повний текст джерелаEl-Ossaily, Yasser A., Nuha M. M. Alanazi, Ibrahim O. Althobaiti, Hamud A. Altaleb, Nayef S. Al-Muailkel, Mohamed Y. El-Sayed, Modather F. Hussein, et al. "Multicomponent approach to the synthesis and spectral characterization of some 3,5-pyrazolididione derivatives and evaluation as anti-inflammatory agents." Current Chemistry Letters 13, no. 1 (2024): 127–40. http://dx.doi.org/10.5267/j.ccl.2023.8.003.
Повний текст джерелаYuan, Huijun, Yao Li, Hanhui Zhao, Zhihong Yang, Xin Li, and Wenjun Li. "Asymmetric synthesis of atropisomeric pyrazole via an enantioselective reaction of azonaphthalene with pyrazolone." Chemical Communications 55, no. 84 (2019): 12715–18. http://dx.doi.org/10.1039/c9cc06360a.
Повний текст джерелаA. Almehizia, Abdulrahman, Ahmad M. Naglah, Amer A. Zen, Tamer K. Khatab, and 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, no. 4 (April 30, 2024): 1119–27. http://dx.doi.org/10.4314/bcse.v38i4.24.
Повний текст джерелаLi, Jun-Hua, and Da-Ming Du. "Enantioselective synthesis of chiral heterocycles containing both chroman and pyrazolone derivatives catalysed by a chiral squaramide." Organic & Biomolecular Chemistry 13, no. 20 (2015): 5636–45. http://dx.doi.org/10.1039/c4ob02653e.
Повний текст джерелаHamama, Wafaa S., Mohamed A. Ismail, Hana’a A. Al-Saman, and Hanafi H. Zoorob. "Convenient Selective Synthesis of Substituted Pyrido[2,3-d]pyrimidones and Annulated Derivatives." Zeitschrift für Naturforschung B 62, no. 1 (January 1, 2007): 104–10. http://dx.doi.org/10.1515/znb-2007-0115.
Повний текст джерелаHassan, Alaa A., Yusria R. Ibrahim, and Ahmed M. Shawky. "Reactions of Substituted Carbohydrazides with Electron-poor Olefins." Zeitschrift für Naturforschung B 63, no. 8 (August 1, 2008): 998–1004. http://dx.doi.org/10.1515/znb-2008-0813.
Повний текст джерелаLeleu-Chavain, Natascha, Romain Regnault, Hania Ahouari, Raphaël Le Biannic, Mostafa Kouach, Frédérique Klupsch, Romain Magnez, et al. "Antioxidant Properties and Aldehyde Reactivity of PD-L1 Targeted Aryl-Pyrazolone Anticancer Agents." Molecules 27, no. 10 (May 21, 2022): 3316. http://dx.doi.org/10.3390/molecules27103316.
Повний текст джерелаCho, Joungmo, Venkata Subbaiah Sadu, Yohan Han, Yunsoo Bae, Hwajeong Lee, and Kee-In Lee. "Structural Requirements of 1-(2-Pyridinyl)-5-pyrazolones for Disproportionation of Boronic Acids." Molecules 26, no. 22 (November 11, 2021): 6814. http://dx.doi.org/10.3390/molecules26226814.
Повний текст джерелаMahajan, Suruchi, Pankaj Chauhan, Uğur Kaya, Kristina Deckers, Kari Rissanen та Dieter Enders. "Enantioselective synthesis of pyrazolone α-aminonitrile derivatives via an organocatalytic Strecker reaction". Chemical Communications 53, № 49 (2017): 6633–36. http://dx.doi.org/10.1039/c7cc02874a.
Повний текст джерелаShyshkina, Olena O., Volodymyr V. Medviediev, Oleg V. Shishkin, Andrii I. Kysil, and Yulian M. Volovenko. "Unexpected synthesis of pyrazolone derivatives." Tetrahedron 71, no. 8 (February 2015): 1283–86. http://dx.doi.org/10.1016/j.tet.2014.12.082.
Повний текст джерелаAchuthanandhan, Jyothi, and Baskar Lakshmanan. "Docking studies of tetra substituted pyrazolone derivatives as potential antiviral agents." JOURNAL OF PHARMACEUTICAL CHEMISTRY 5, no. 2 (December 20, 2018): 5–8. http://dx.doi.org/10.14805/jphchem.2018.art103.
Повний текст джерелаParveen, Mehtab, Shaista Azaz, Ali Mohammed Malla, Faheem Ahmad, Musheer Ahmad, and 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, no. 1 (2016): 148–62. http://dx.doi.org/10.1039/c5ra21146h.
Повний текст джерелаAhmed, Badie, and Jasim Abdullah. "Ultrasound Assisted Synthesis Of Pyrazolone Derivatives." JOURNAL OF EDUCATION AND SCIENCE 26, no. 5 (December 1, 2013): 57–63. http://dx.doi.org/10.33899/edusj.2013.163055.
Повний текст джерелаPavlov, P. T., A. F. Goleneva, A. E. Lesnov, and T. S. Prokhorova. "Biological activity of some pyrazolone derivatives." Pharmaceutical Chemistry Journal 32, no. 7 (July 1998): 370–72. http://dx.doi.org/10.1007/bf02645994.
Повний текст джерелаIshihara, Yoshimi, Takeyuki Ito, Hiroshi Saito, and Jiro Takano. "Reaction of acridine with pyrazolone derivatives." Journal of Heterocyclic Chemistry 42, no. 5 (July 2005): 963–67. http://dx.doi.org/10.1002/jhet.5570420533.
Повний текст джерелаZonouz, Adeleh Moshtaghi, Masoumeh Beiranvand, Rahim Mohammad-Rezaei, and Soheila Naderi. "Green and Efficient Synthesis of Fluorescent Bis(pyrazolyl)methanes in Choline Chloride/Urea Deep Eutectic Solvent." Letters in Organic Chemistry 17, no. 7 (July 7, 2020): 548–54. http://dx.doi.org/10.2174/1570178617666191111121813.
Повний текст джерелаKashinath, Dhurke, Kota Sathish, and 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, no. 02 (April 13, 2021): 123–33. http://dx.doi.org/10.1055/a-1480-9837.
Повний текст джерелаGuo, Jixi, Yucai Zhang, Dianzeng Jia, Mingxi Guo, and Yinhua Li. "Design and synthesis of reversible solid-state photochromic pyrazolones by introducing a pyridine ring." Photochemical & Photobiological Sciences 15, no. 10 (2016): 1222–26. http://dx.doi.org/10.1039/c6pp00119j.
Повний текст джерелаWang, Jun, Guan-Cheng Xu, Yan-Ping Zhang, Hua-Ying Luo, Jin-Yao Li, Li Zhang, and 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, no. 6 (2019): 2529–39. http://dx.doi.org/10.1039/c8nj02695e.
Повний текст джерелаDeyab, M. A., A. S. Fouda, M. M. Osman, and S. Abdel-Fattah. "Mitigation of acid corrosion on carbon steel by novel pyrazolone derivatives." RSC Advances 7, no. 71 (2017): 45232–40. http://dx.doi.org/10.1039/c7ra08761f.
Повний текст джерелаAo, Chaoqun, Jingjing Huang, Xinfang Xu, Shikun Jia, Zhenghui Kang, and Wenhao Hu. "A Rh-catalyzed three-component reaction for the diastereoselective synthesis of pyrazolone derivatives with contiguous quaternary stereocenters." Organic & Biomolecular Chemistry 18, no. 18 (2020): 3466–70. http://dx.doi.org/10.1039/d0ob00482k.
Повний текст джерелаMarzouk, Magda Ismail, Galal Hosni Sayed, Mohamed Said Abd ElHalim, and Salma Yehia Mansour. "Synthesis and characterization of novel pyrazolone derivatives." European Journal of Chemistry 5, no. 1 (March 31, 2014): 24–32. http://dx.doi.org/10.5155/eurjchem.5.1.24-32.870.
Повний текст джерелаRadini, Ibrahim. "Design, Synthesis, and Antimicrobial Evaluation of Novel Pyrazoles and Pyrazolyl 1,3,4-Thiadiazine Derivatives." Molecules 23, no. 9 (August 21, 2018): 2092. http://dx.doi.org/10.3390/molecules23092092.
Повний текст джерелаDe Crescentini, L., F. R. Perrulli, G. Favi, S. Santeusanio, G. Giorgi, O. A. Attanasi, and 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, no. 37 (2016): 8674–78. http://dx.doi.org/10.1039/c6ob01595f.
Повний текст джерелаLi, Jun-Hua, and Da-Ming Du. "Correction: Enantioselective synthesis of chiral heterocycles containing both chroman and pyrazolone derivatives catalysed by a chiral squaramide." Organic & Biomolecular Chemistry 13, no. 26 (2015): 7337. http://dx.doi.org/10.1039/c5ob90099a.
Повний текст джерелаMOHAMMAD, Abeer Essa, Munther Abduljaleel MUHAMMAD-ALI, and 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, no. 42 (October 11, 2022): 12–28. http://dx.doi.org/10.52571/ptq.v19.n42.2022.02_munther_pgs_12_28.pdf.
Повний текст джерелаRegnault, Romain, Frédérique Klupsch, Hassiba El-Bouazzati, Romain Magnez, Raphaël Le Biannic, Natascha Leleu-Chavain, Hania Ahouari, et al. "Novel PD-L1-Targeted Phenyl-Pyrazolone Derivatives with Antioxidant Properties." Molecules 28, no. 8 (April 15, 2023): 3491. http://dx.doi.org/10.3390/molecules28083491.
Повний текст джерелаSun, Bing-Bing, Jun-Bo Chen, Jun-Qi Zhang, Xiao-Peng Yang, Hao-Peng Lv, Zheng Wang, and Xing-Wang Wang. "Organo-catalyzed asymmetric cascade annulation reaction for the construction of bi-spirocyclic pyrazolone and oxindole derivatives." Organic Chemistry Frontiers 7, no. 5 (2020): 796–809. http://dx.doi.org/10.1039/d0qo00001a.
Повний текст джерелаArora, Kishor. "In-Silico QSAR Studies of Some Pyrazolone Compounds." European Journal of Advanced Chemistry Research 4, no. 4 (October 18, 2023): 1–8. http://dx.doi.org/10.24018/ejchem.2023.4.4.148.
Повний текст джерелаEl-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, № 8 (1 травня 2016): 311–17. http://dx.doi.org/10.24297/jac.v12i8.2840.
Повний текст джерелаEl-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, № 1 (19 квітня 2008): 311–17. http://dx.doi.org/10.24297/jac.v4i1.960.
Повний текст джерелаAshtekar, Harsha, Prarambh S. R. Dwivedi, Natasha Aggarwal, Zeena Fernandes, and 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, no. 01 (March 25, 2023): 1–9. http://dx.doi.org/10.25258/ijddt.13.1.01.
Повний текст джерелаYoon, Sanghyun, Byunghun Choi, Md Morshedur Rahman, Santosh Kumar, Shekh Md Mamun Kabir, and 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, no. 24 (December 14, 2019): 4209. http://dx.doi.org/10.3390/ma12244209.
Повний текст джерелаPégurier, Cécile, Philippe Collart, Pierre Danhaive, Sabine Defays, Michel Gillard, Frédéric Gilson, Thierry Kogej, et al. "Pyrazolone methylamino piperidine derivatives as novel CCR3 antagonists." Bioorganic & Medicinal Chemistry Letters 17, no. 15 (August 2007): 4228–31. http://dx.doi.org/10.1016/j.bmcl.2007.05.035.
Повний текст джерелаWang, Jin-Jun, Bing-Zhu Yin, Gui-Ji Jiang, and Kimiaki Imafuku. "Synthesis of isochroman-fused pyrazolone and pyrimidine derivatives." Journal of Heterocyclic Chemistry 27, no. 5 (July 1990): 1181–84. http://dx.doi.org/10.1002/jhet.5570270504.
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