Статті в журналах з теми "C]pyrazole"
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Ознайомтеся з топ-50 статей у журналах для дослідження на тему "C]pyrazole".
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Abaszadeh, Mehdi, Hassan Sheibani, and Kazem Saidi. "The Condensation of (Chlorocarbonyl)phenyl Ketene with Bisnucleophiles. Synthesis of 4-Hydroxy-5-phenylpyro-[2,3-c]pyrazol-6-ones and Formation of Pyrazolo[1,2-a]pyrazole-triones by Hydrogen Exchange in Unstable Mesoionic Compounds." Australian Journal of Chemistry 63, no. 1 (2010): 92. http://dx.doi.org/10.1071/ch09344.
Повний текст джерелаSophy, Mohamed Ahmed Elian, and Mohamed Ahmed Mahmoud Abdel Reheim. "Synthesis of Some New 1, 3, 4-Oxadiazole, Pyrazole, and Pyrimidine Bearing Thienopyrazole Moieties." Current Organic Synthesis 17, no. 8 (October 28, 2020): 661–70. http://dx.doi.org/10.2174/1570179417999200730215318.
Повний текст джерелаLindsay-Scott, Peter J., and Eloise Rivlin-Derrick. "Regiocontrolled Synthesis of 6,7-Dihydro-4H-pyrazolo[5,1-c][1,4]oxazines." Synthesis 52, no. 01 (October 8, 2019): 105–18. http://dx.doi.org/10.1055/s-0037-1610734.
Повний текст джерелаGerster, Holger, Michael Keim, and Gerhard Maas. "Cycloaddition reactions of acetylenic iminium salts and diazoacetates leading to pyrazole iminium salts." Zeitschrift für Naturforschung B 74, no. 4 (April 24, 2019): 347–55. http://dx.doi.org/10.1515/znb-2019-0001.
Повний текст джерелаBertolasi, Valerio, Paola Gilli, Valeria Ferretti, Gastone Gilli, and Cristina Fernàndez-Castaño. "Self-assembly of NH-pyrazoles via intermolecular N—H...N hydrogen bonds." Acta Crystallographica Section B Structural Science 55, no. 6 (December 1, 1999): 985–93. http://dx.doi.org/10.1107/s0108768199004966.
Повний текст джерелаMilišiūnaitė, Vaida, Rūta Paulavičiūtė, Eglė Arbačiauskienė, Vytas Martynaitis, Wolfgang Holzer, and Algirdas Šačkus. "Synthesis of 2H-furo[2,3-c]pyrazole ring systems through silver(I) ion-mediated ring-closure reaction." Beilstein Journal of Organic Chemistry 15 (March 14, 2019): 679–84. http://dx.doi.org/10.3762/bjoc.15.62.
Повний текст джерелаThirunarayanan, Ganesamoorthy, and K. Ravi. "Synthesis and Spectral Correlation Study of some 3-(3,4-dichlorophenyl)-5-(Substituted Phenyl)-4,5-dihydro-1H-Pyrazole-1-yl-Ethanones." International Letters of Chemistry, Physics and Astronomy 19 (October 2013): 44–57. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.19.44.
Повний текст джерелаLerner, Hans-Wolfram, Günter Margraf, Tonia Kretz, Olav Schiemann, Jan W. Bats, Gerd Dürner, Fabrizia Fabrizi de Biani, Piero Zanello, Michael Boltea, and Matthias Wagner. "Redox Behaviour of Pyrazolyl-Substituted 1,4-Dihydroxyarenes: Formation of the Corresponding Semiquinones, Quinhydrones and Quinones." Zeitschrift für Naturforschung B 61, no. 3 (March 1, 2006): 252–64. http://dx.doi.org/10.1515/znb-2006-0304.
Повний текст джерелаRamadan, El Sayed, Essam M. Sharshira, Ramadan I. El Sokkary, and Noussa Morsy. "Synthesis and antimicrobial evaluation of some heterocyclic compounds from 3-aryl-1-phenyl-1H-pyrazole-4-carbaldehydes." Zeitschrift für Naturforschung B 73, no. 6 (June 27, 2018): 389–97. http://dx.doi.org/10.1515/znb-2018-0009.
Повний текст джерелаÇetin, Adnan, Ishak Bildirici, and Selçuk Gümüş. "Novel Pyrazole Derivatives Having Mono/Di Chiral Centered Group as Organocatalyst for Henry Reaction." Macedonian Journal of Chemistry and Chemical Engineering 39, no. 1 (June 9, 2020): 17. http://dx.doi.org/10.20450/mjcce.2020.1954.
Повний текст джерелаRizk, Sameh, Ismail M. Awheda, and Fathi A. Smida. "Synthesis and DFT Study of Newly Schiff Base and Fused Heterocyclic Compounds as Antibacterial Agent." JOURNAL OF ADVANCES IN CHEMISTRY 16 (November 7, 2019): 5395–403. http://dx.doi.org/10.24297/jac.v16i0.8499.
Повний текст джерелаHosny, Mona A., Yasser H. Zaki, Wafaa A. Mokbel, and Abdou O. Abdelhamid. "Synthesis, Characterization, Antimicrobial Activity and Anticancer of Some New Pyrazolo[1,5-a]pyrimidines and Pyrazolo[5,1-c]1,2,4-triazines." Medicinal Chemistry 16, no. 6 (September 7, 2020): 750–60. http://dx.doi.org/10.2174/1573406415666190620144404.
Повний текст джерелаDeeb, Ali, Medhat El-Mobayed, Abdel Naby Essawy, Adel Abd El-Hamid, and Atef Mohamid Abd El-Hamid. "Heterocyclic synthesis from 3-amino-4-cyanopyrazole." Collection of Czechoslovak Chemical Communications 55, no. 3 (1990): 728–33. http://dx.doi.org/10.1135/cccc19900728.
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 джерелаIBRAHIM, M. K. A., A. H. H. ELGHANDOUR, G. S. M. ABDEL-SAYED, and A. S. M. ABDEL FATTAH. "ChemInform Abstract: Synthesis of Pyrazoles and Fused Pyrazoles. Novel Synthesis of Pyrano[2,3-c]pyrazole, Thieno[2,3-c]pyrazole and Pyrazolo[3,4-b]pyridine Derivatives." ChemInform 29, no. 27 (June 21, 2010): no. http://dx.doi.org/10.1002/chin.199827039.
Повний текст джерелаRoman, Gheorghe. "2-Naphthol-pyrazole conjugates as substrates in the Mannich reaction." Zeitschrift für Naturforschung B 73, no. 5 (May 24, 2018): 275–80. http://dx.doi.org/10.1515/znb-2017-0209.
Повний текст джерелаKang, Eunsu, Hyun Tae Kim, and Jung Min Joo. "Transition-metal-catalyzed C–H functionalization of pyrazoles." Organic & Biomolecular Chemistry 18, no. 32 (2020): 6192–210. http://dx.doi.org/10.1039/d0ob01265c.
Повний текст джерелаSabah, Rusul Saad, Zahraa S. Al-Garawi, and Mahmoud N. Al-jibouri. "The utilities of pyrazolines encouraged synthesis of a new pyrazoline derivative via ring closure of chalcone, for optimistic neurodegenerative applications." Al-Mustansiriyah Journal of Science 33, no. 1 (March 10, 2022): 21–31. http://dx.doi.org/10.23851/mjs.v33i1.1067.
Повний текст джерелаRazmienė, Beatričė, Eva Řezníčková, Vaida Dambrauskienė, Radek Ostruszka, Martin Kubala, Asta Žukauskaitė, Vladimír Kryštof, Algirdas Šačkus, and Eglė Arbačiauskienė. "Synthesis and Antiproliferative Activity of 2,4,6,7-Tetrasubstituted-2H-pyrazolo[4,3-c]pyridines." Molecules 26, no. 21 (November 8, 2021): 6747. http://dx.doi.org/10.3390/molecules26216747.
Повний текст джерелаAbeed, Ahmed A. O., Talaat I. El-Emary, and Mohamed S. K. Youssef. "A Facile Synthesis and Reactions of Some Novel Pyrazole-based Heterocycles." Current Organic Synthesis 16, no. 3 (June 17, 2019): 405–12. http://dx.doi.org/10.2174/1570179416666181210160908.
Повний текст джерелаFrampton, Christopher S., Michael W. Majchrzak, and John Warkentin. "Sense of sequential 1,5-sigmatropic rearrangements of dimethyl-3,3-dialkyl-3H-pyrazole-4,5-dicarboxylates. Crystal and molecular structures of two dimethyl-4,5-dialkyl-1H-pyrazole-1,3-dicarboxylates." Canadian Journal of Chemistry 69, no. 3 (March 1, 1991): 373–78. http://dx.doi.org/10.1139/v91-057.
Повний текст джерелаMandour, Adel, Eslam El-Sawy, Manal Ebaid, and Seham Hassan. "Synthesis and potential biological activity of some novel 3-[(N-substituted indol-3-yl)methyleneamino]-6-amino-4-aryl-pyrano(2,3-c)pyrazole-5-carbonitriles and 3,6-diamino-4-(N-substituted indol-3-yl)pyrano(2,3-c)pyrazole-5-carbonitriles." Acta Pharmaceutica 62, no. 1 (March 1, 2012): 15–30. http://dx.doi.org/10.2478/v10007-012-0007-0.
Повний текст джерелаUsami, Yoshihide, Kodai Sumimoto, Azusa Kishima, Yuya Tatsui, Hiroki Yoneyama, and Shinya Harusawa. "Synthesis of Dihydropyrano[3,2-c]pyrazoles via Double Bond Migration and Ring-Closing Metathesis." Molecules 24, no. 2 (January 15, 2019): 296. http://dx.doi.org/10.3390/molecules24020296.
Повний текст джерелаDodiya, Dipti, Amit Trivedi, Samir Jarsania, Shailesh Vaghasia, and Viresh Shah. "Characterization and biological evaluation of some novel pyrazolo[3',4':4,5]thieno[2,3-d]pyrimidin-8-ones synthesized via the Gewald reaction." Journal of the Serbian Chemical Society 73, no. 7 (2008): 683–90. http://dx.doi.org/10.2298/jsc0807683d.
Повний текст джерелаDotsenko, Victor V., Vladimir A. Dushenko, Nikolai A. Aksenov, Inna V. Aksenova, and Evgeniy E. Netreba. "The First Synthesis of [1,2]oxaphosphinino[6,5-c]pyrazoles by Thiophosphorylation of 6-Aminopyrano[2,3-c]pyrazole-5-Carbonitriles." Proceedings 9, no. 1 (November 14, 2018): 26. http://dx.doi.org/10.3390/ecsoc-22-05680.
Повний текст джерелаRastogi, Sameer, Tarun Virmani, Charan Deshwal, and Joyti Gupta. "Novel Synthesis of Functionally Substituted Pyrazole and Biological Evaluation." Volume 1, Issue 1 : October 2015 – December 2015 1, no. 1 (November 15, 2015): 18–22. http://dx.doi.org/10.32463/rphs.2015.v01i01.04.
Повний текст джерелаMokhonova, Inna D., Evgenij A. Maksimov, Irina V. Ledenyona, Alevtina Y. Yegorova, and Khidmet S. Shikhaliev. "Reactions of 3H-furan-2-ones and 2H-chromen-2-ones with pyrazole-3(5)-diazonium salts." Heterocyclic Communications 24, no. 4 (August 28, 2018): 183–85. http://dx.doi.org/10.1515/hc-2017-0192.
Повний текст джерелаKulkarni, Pravin S., Swapnil R. Sarda, Amol U. Khandebharad, Mazahar Farooqui, and Brijmohan R. Agrawal. "Synthesis and Biological Screening of Novel 5-(5-Aryl-1-phenyl-1H-pyrazol-3-yl)-3-aryl-1,2,4-oxadiazole Derivatives." Asian Journal of Chemistry 34, no. 1 (2021): 209–15. http://dx.doi.org/10.14233/ajchem.2022.23497.
Повний текст джерелаBustos, Carlos, Luis Alvarez-Thon, Tania Oportus, Angela Mesías-Salazar, and Ricardo Baggio. "On substituted pyrazole derivatives. II. (E)-1-(4-{[1-(4-Fluorophenyl)-3,5-dimethyl-1H-pyrazol-4-yl]diazenyl}phenyl)ethanone and (E)-1-(4-chlorophenyl)-3,5-dimethyl-4-[2-(2-nitrophenyl)diazenyl]-1H-pyrazole." Acta Crystallographica Section C Structural Chemistry 71, no. 1 (January 1, 2015): 53–58. http://dx.doi.org/10.1107/s2053229614024619.
Повний текст джерелаFrey, Guido D., Wolfgang W. Schoeller, and Eberhardt Herdtweck. "Solid-state and Calculated Electronic Structure of 4-Acetylpyrazole." Zeitschrift für Naturforschung B 69, no. 7 (July 1, 2014): 839–43. http://dx.doi.org/10.5560/znb.2014-4064.
Повний текст джерелаHerfindo, Noval, Riska Prasetiawati, Daniel Sialagan, Neni Frimayanti та Adel Zamri. "Synthesis, Antiproliferative Activity and Molecular Docking Studies of 1,3,5-Triaryl Pyrazole Compound as Estrogen α Receptor Inhibitor Targeting MCF-7 Cells Line". Molekul 15, № 1 (23 березня 2020): 18. http://dx.doi.org/10.20884/1.jm.2020.15.1.585.
Повний текст джерелаHafez, Hend N., and Abdel-Rhman B. A. El-Gazzar. "Synthesis of pyranopyrazolo N-glycoside and pyrazolopyranopyrimidine C-glycoside derivatives as promising antitumor and antimicrobial agents." Acta Pharmaceutica 65, no. 3 (September 1, 2015): 215–33. http://dx.doi.org/10.1515/acph-2015-0022.
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 джерелаTaguchi, Alexander, Oleksandr Kokhan, and Colin Wraight. "Pyrazole Cytochrome C Complexes." Biophysical Journal 102, no. 3 (January 2012): 466a—467a. http://dx.doi.org/10.1016/j.bpj.2011.11.2559.
Повний текст джерелаDing, Zhengwei, Qitao Tan, Mingchun Gao, and Bin Xu. "Copper-catalyzed aerobic cascade cycloamination and acyloxylation: a direct approach to 4-acyloxy-1H-pyrazoles." Organic & Biomolecular Chemistry 13, no. 16 (2015): 4642–46. http://dx.doi.org/10.1039/c5ob00409h.
Повний текст джерелаAbunada, Nada M., Hamdi M. Hassaneen, Ahmed S. M. Abu Samaha, and Omar A. Miqdad. "Synthesis and antimicrobial evaluation of some new pyrazole, pyrazoline and chromeno[3,4-c]pyrazole derivatives." Journal of the Brazilian Chemical Society 20, no. 5 (2009): 975–87. http://dx.doi.org/10.1590/s0103-50532009000500024.
Повний текст джерелаDalal, Kiran S., Yogesh A. Tayade, Yogesh B. Wagh, Darshak R. Trivedi, Dipak S. Dalal, and Bhushan L. Chaudhari. "Bovine serum albumin catalyzed one-pot, three-component synthesis of dihydropyrano[2,3-c]pyrazole derivatives in aqueous ethanol." RSC Advances 6, no. 18 (2016): 14868–79. http://dx.doi.org/10.1039/c5ra13014j.
Повний текст джерелаBiswas, Swapan Kumar, and Debasis Das. "One-pot Synthesis of Pyrano[2,3-c]pyrazole Derivatives via Multicomponent Reactions (MCRs) and their Applications in Medicinal Chemistry." Mini-Reviews in Organic Chemistry 19, no. 5 (August 2022): 552–68. http://dx.doi.org/10.2174/1570193x19666211220141622.
Повний текст джерелаPrhavc, Marija, and Jože Kobe. "SYNTHESIS OF PYRAZOLO[4,3-C]PYRIDINE C-RIBONUCLEOSIDESVIAAN EFFECTIVE TETRAZOLE TO PYRAZOLE TRANSFORMATION." Nucleosides and Nucleotides 15, no. 11-12 (November 1996): 1779–95. http://dx.doi.org/10.1080/07328319608002732.
Повний текст джерелаSikandar, Sana, Ameer Fawad Zahoor, Sajjad Ahmad, Muhammad Naveed Anjum, Mirza Nadeem Ahmad, and Muhammad Sami Ullah Shah. "L-Cysteine Catalyzed Environmentally Benign One-pot Multicomponent Approach Towards the Synthesis of Dihydropyrano[2,3-c]pyrazole Derivatives." Current Organic Synthesis 17, no. 6 (September 25, 2020): 457–63. http://dx.doi.org/10.2174/1570179417666200511092332.
Повний текст джерелаHrynyshyn, Yevhenii, Hanna Musiichuk, Olena Komarovska-Porokhnyavets, Oksana Is’kiv, Nataliia Moskalenko, Maryna Stasevych, Nazar Tsyzoryk, and Mykhailo Vovk. "Synthesis and Antimicrobial Activity of 4-Arylthio- and 4 Alkylthiofunctionalized Pyrazolo[1,5-a]pyrazines." Ukrainian Chemistry Journal 85, no. 1 (February 15, 2019): 58–66. http://dx.doi.org/10.33609/0041-6045.85.1.2019.58-66.
Повний текст джерелаKantlehner, Willi, Jochen Mezger, Rüdiger Stieglitz, Kai Edelmann, Hansjörg Lehmann, Markus Vettel, Ralf Kreß, Wolfgang Frey, and Sebastian Ladendorf. "Orthoamide, LXV [1]. Kondensationsreaktionen von Amidinen, Guanidinen, Hydrazin und Hydrazin-Derivaten mit Orthoamiden von Alkincarbonsäuren / Orthoamides,LXV [1]. Condensation Reactions of Amidines, Guanidines, Hydrazine and Hydrazine Derivatives with Orthoamides of Alkyne Carboxylic Acids." Zeitschrift für Naturforschung B 62, no. 8 (August 1, 2007): 1015–29. http://dx.doi.org/10.1515/znb-2007-0804.
Повний текст джерелаZhang, Shijie, Zhenguo Gao, Di Lan, Qian Jia, Ning Liu, Jiaoqiang Zhang, and Kaichang Kou. "Recent Advances in Synthesis and Properties of Nitrated-Pyrazoles Based Energetic Compounds." Molecules 25, no. 15 (July 30, 2020): 3475. http://dx.doi.org/10.3390/molecules25153475.
Повний текст джерелаWang, Yu-Feng, Chun-Hua Yu та Run-Qiang Zhu. "An iron(III) complex salt containing pyrazole as both ligand and counter-ion: bis(1H-pyrazol-2-ium) pentacyanido(1H-pyrazole-κN 2)ferrate(III)". Acta Crystallographica Section C Structural Chemistry 70, № 5 (9 квітня 2014): 437–39. http://dx.doi.org/10.1107/s2053229614007128.
Повний текст джерелаMague, Joel T., Shaaban K. Mohamed, Mehmet Akkurt, Talaat I. El-Emary, and Mustafa R. Albayati. "Crystal structure of 5-(4,5-dihydro-1H-imidazol-2-yl)-3-methyl-1-phenyl-1H-pyrazolo[3,4-b]pyrazin-6-amine." Acta Crystallographica Section E Structure Reports Online 70, no. 11 (October 31, 2014): o1212—o1213. http://dx.doi.org/10.1107/s160053681402354x.
Повний текст джерелаHassan, Alaa A., Nasr K. Mohamed, Ahmed M. Shawkya, and Dietrich Döpp. "Pyrazole, pyrazolo[1,2-c]-1,3,4-thiadiazole and thiadiazepine derivatives from thiosemicarbazides." Arkivoc 2003, no. 1 (July 10, 2003): 118–28. http://dx.doi.org/10.3998/ark.5550190.0004.114.
Повний текст джерелаKoraiem, Ahmed I. M. "The synthesis of pyrazolo- and isoxazolo-[3,4-c]-pyrazole hemiazadicarbocyanine dyes." Journal of Chemical Technology and Biotechnology. Chemical Technology 34, no. 2 (May 29, 2007): 43–50. http://dx.doi.org/10.1002/jctb.5040340202.
Повний текст джерелаSharma, Naresh, Sanjay Parihar, R. N. Jadeja, Rajni Kant, and Vivek K. Gupta. "Crystal structure of (Z)-1-(3,4-dichlorophenyl)-3-methyl-4-[(naphthalen-1-ylamino)(p-tolyl)methylidene]-1H-pyrazol-5(4H)-one." Acta Crystallographica Section E Structure Reports Online 70, no. 9 (August 1, 2014): o955—o956. http://dx.doi.org/10.1107/s1600536814017140.
Повний текст джерелаSu, Ping, Xue-gang Song, Ren-qiang Sun, and Xing-man Xu. "Hydrogen bonding in the crystal structure of the molecular salt of pyrazole–pyrazolium picrate." Acta Crystallographica Section E Crystallographic Communications 72, no. 6 (May 27, 2016): 861–63. http://dx.doi.org/10.1107/s2056989016008215.
Повний текст джерелаPalka, Barbara, Angela Di Capua, Maurizio Anzini, Gyté Vilkauskaité, Algirdas Šačkus, and Wolfgang Holzer. "Synthesis of trifluoromethyl-substituted pyrazolo[4,3-c]pyridines – sequential versus multicomponent reaction approach." Beilstein Journal of Organic Chemistry 10 (July 31, 2014): 1759–64. http://dx.doi.org/10.3762/bjoc.10.183.
Повний текст джерела