Статті в журналах з теми "Pyrazole-4"
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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 джерелаHartwig de Oliveira, Daniela, Fernanda Severo Sabedra Sousa, Paloma Taborda Birmann, Ana Paula Pesarico, Diego Alves, Raquel Guimarães Jacob, and Lucielli Savegnago. "Evaluation of antioxidant activity and toxicity of sulfur- or selenium-containing 4-(arylchalcogenyl)-1H-pyrazoles." Canadian Journal of Physiology and Pharmacology 98, no. 7 (July 2020): 441–48. http://dx.doi.org/10.1139/cjpp-2019-0356.
Повний текст джерелаAlsayari, Abdulrhman, Abdullatif Bin Muhsinah, Yahya I. Asiri, Jaber Abdullah Alshehri, Yahia N. Mabkhot, Mohammad Y. Alfaifi, Serag Eldin I. Elbehairi, Mater H. Mahnashi, and Mohd Zaheen Hassan. "Arylhydrazono/Aryldiazenyl Pyrazoles: Green One-Pot Solvent-Free Synthesis and Anticancer Evaluation." Letters in Organic Chemistry 17, no. 10 (November 17, 2020): 772–78. http://dx.doi.org/10.2174/1570178617666200320104923.
Повний текст джерелаAndicsová, Anita, Angelika Lásiková, Marek Fronc, Jozef Kožíšek, and Daniel Végh. "3-(2-Heteroaryl)-pyrazolotetrazoles – a subunits for losartan-like structures." Acta Chimica Slovaca 5, no. 2 (November 1, 2012): 220–24. http://dx.doi.org/10.2478/v10188-012-0033-z.
Повний текст джерелаSrinivasa Reddy, T., Hitesh Kulhari, V. Ganga Reddy, A. V. Subba Rao, Vipul Bansal, Ahmed Kamal, and Ravi Shukla. "Synthesis and biological evaluation of pyrazolo–triazole hybrids as cytotoxic and apoptosis inducing agents." Organic & Biomolecular Chemistry 13, no. 40 (2015): 10136–49. http://dx.doi.org/10.1039/c5ob00842e.
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 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 джерелаDeacon, Glen B., Peter C. Junk, and Aron Urbatsch. "Lanthanoid and Alkaline Earth Complexes Involving New Substituted Pyrazolates." Australian Journal of Chemistry 65, no. 7 (2012): 802. http://dx.doi.org/10.1071/ch12069.
Повний текст джерелаLam, Linh, Sang H. Park, and Joseph Sloop. "Synthesis and Characterization of 3-Methyl-1-(4-(trifluoromethyl)phenyl)indeno [1,2-c]pyrazol-4(1H)-one." Molbank 2022, no. 4 (November 7, 2022): M1483. http://dx.doi.org/10.3390/m1483.
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 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 джерелаChirkova, Zhanna V., Sergey I. Filimonov, and Igor G. Abramov. "SYNTHESIS OF BENZOFURAN-5,6-DICARBONITRILES ANNELATED WITH PYRAZOLE CYCLE." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 60, no. 6 (July 19, 2017): 45. http://dx.doi.org/10.6060/tcct.2017606.5576.
Повний текст джерелаMcfadden, HG, and JL Huppatz. "Synthesis of (Pyrazol-4-yl)alkanones and Alkylpyrazole-4-Carbonitriles." Australian Journal of Chemistry 44, no. 9 (1991): 1263. http://dx.doi.org/10.1071/ch9911263.
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 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 джерелаLamie, Phoebe F. "Synthesis and Antimicrobial Activity of some Novel Isoindoline-1,3-Dione Derivatives." JOURNAL OF ADVANCES IN CHEMISTRY 8, no. 2 (March 2, 2008): 1660–66. http://dx.doi.org/10.24297/jac.v8i2.5570.
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 джерелаRue, Kelly L., Susana Herrera, Indranil Chakraborty, Alexander M. Mebel, and Raphael G. Raptis. "Completion of Crystallographic Data for the Series of 4-Halogenated-1H-pyrazoles: Crystal Structure Determination of 4-Iodo-1H-pyrazole and Spectroscopic Comparison." Crystals 13, no. 7 (July 14, 2023): 1101. http://dx.doi.org/10.3390/cryst13071101.
Повний текст джерелаQiao, Li, Peng-Peng Cai, Zhong-Hua Shen, Hong-Ke Wu, Cheng-Xia Tan, Jian-Quan Weng, and Xing-Hai Liu. "Crystal structure and molecular docking studies of new pyrazole-4-carboxamides." Heterocyclic Communications 25, no. 1 (May 11, 2019): 66–72. http://dx.doi.org/10.1515/hc-2019-0012.
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 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 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 джерелаWarkentin, John, та John Mck R. Woollard. "Photolysis of 5,5-dibenzyl-Δ3-1,3,4-oxadiazolines". Canadian Journal of Chemistry 75, № 3 (1 березня 1997): 289–307. http://dx.doi.org/10.1139/v97-033.
Повний текст джерелаJasril, Jasril, Neni Frimayanti, Yuana Nurulita, Adel Zamri, Ihsan Ikhtiarudin, and Guntur Guntur. "5-(4-Fluorophenyl)-3-(naphthalen-1-yl)-1-phenyl-1H-pyrazole." Molbank 2021, no. 1 (March 10, 2021): M1197. http://dx.doi.org/10.3390/m1197.
Повний текст джерелаVeeranki, Krishna Chaitanya, Jalapathi Pochampally, Ravi Chandar Maroju, and Vishnu Thumma. "Synthesis of Novel 4-(3-nitro-2H-chromen-2-yl)-1,3-diphenyl-1H-pyrazole analogues." Research Journal of Chemistry and Environment 27, no. 2 (January 15, 2023): 35–38. http://dx.doi.org/10.25303/2702rjce035038.
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 джерелаErdem, Ahmet, Hasan Genc, Nejdet Sen, Rafet Kilincarslan, and Emin Erdem. "The Synthesis and Reactions of Novel Pyrazole Derivatives by 4-phenylcarbonyl-5-phenyl-2,3-dihydro-2,3-furandione Reacted with Some Hydrazones." Revista de Chimie 68, no. 1 (February 15, 2017): 143–46. http://dx.doi.org/10.37358/rc.17.1.5407.
Повний текст джерелаDotsenko, Victor V., Aminat M. Semenova, and Nicolai A. Aksenov. "New Reactions of 5-Amino-3-(Cyanomethyl)-1H-Pyrazole-4-Carbonitrile." Chemistry Proceedings 3, no. 1 (November 14, 2020): 23. http://dx.doi.org/10.3390/ecsoc-24-08398.
Повний текст джерелаDeepa, M., V. Harinadha Babu, R. Parameshwar, and B. Madhava Reddy. "Synthesis of 3-(1, 3-Diphenyl-1H-pyrazol-4-yl) Propanoic Acids Using Diimide Reduction." E-Journal of Chemistry 9, no. 1 (2012): 420–24. http://dx.doi.org/10.1155/2012/481682.
Повний текст джерелаAbdelhamid, Abdou O., Zeineb H. Ismail, and Anhar Abdel-Aziem. "Reactions with Hydrazonoyl Halides 601: Synthesis of Thieno[2′,3′:4,5] Pyrimidino[1,2-b][1,2,4,5]tetrazines, [1]benzothieno[2′,3′:4,5]pyrimidino [1,2-b][1,2,4,5]tetrazines, Pyrazolo[3′,4′:4,5]pyrimidino[1,2-b] [1,2,4,5]tetrazines and Pyrazolo[3,4-d]pyridazines." Journal of Chemical Research 2007, no. 10 (October 2007): 609–16. http://dx.doi.org/10.3184/030823407x256118.
Повний текст джерелаAbularrage, Nile S., Brian J. Levandowski, and Ronald T. Raines. "Synthesis and Diels–Alder Reactivity of 4-Fluoro-4-Methyl-4H-Pyrazoles." International Journal of Molecular Sciences 21, no. 11 (May 31, 2020): 3964. http://dx.doi.org/10.3390/ijms21113964.
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 джерелаBecerra, Diana, Hugo Rojas, and Juan-Carlos Castillo. "3-(tert-Butyl)-N-(4-methoxybenzyl)-1-methyl-1H-pyrazol-5-amine." Molbank 2021, no. 1 (March 10, 2021): M1196. http://dx.doi.org/10.3390/m1196.
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 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 джерелаYang, Pengju, Hongwei Yang, Ying Zhao, Jie Tang, and Guangbin Cheng. "Novel polynitro azoxypyrazole-based energetic materials with high performance." Dalton Transactions 50, no. 45 (2021): 16499–503. http://dx.doi.org/10.1039/d1dt03357c.
Повний текст джерелаBharathi, R. "In vitro and molecular docking studies of an antiinflammatory scaffold with human peroxiredoxin 5 and tyrosine kinase receptor." Bioinformation 16, no. 11 (November 30, 2020): 929–36. http://dx.doi.org/10.6026/97320630016929.
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 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 джерелаVah, Luka, Tadej Medved, Uroš Grošelj, Marina Klemenčič, Črtomir Podlipnik, Bogdan Štefane, Jernej Wagger, Marko Novinec, and Jurij Svete. "Regioselective Synthesis of 5- and 3-Hydroxy-N-Aryl-1H-Pyrazole-4-Carboxylates and Their Evaluation as Inhibitors of Plasmodium falciparum Dihydroorotate Dehydrogenase." Molecules 27, no. 15 (July 25, 2022): 4764. http://dx.doi.org/10.3390/molecules27154764.
Повний текст джерелаTangeti, Venkata S., Kattaru R. Babu, Dasari Vasundhara, K. V. V. V. Satyanarayana, Himabindu Mylapalli, and Kaja S. P. Kumar. "One Pot Synthesis of Novel Substituted 2',4'-Dihydrospiro[chroman-2,3'-pyrazol]-4- one Derivatives." Current Organic Synthesis 15, no. 2 (April 24, 2018): 267–74. http://dx.doi.org/10.2174/1570179414666171011161836.
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 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 джерелаAlsayari, Abdulrhman, Yahya I. Asiri, Abdullatif Bin Muhsinah, and Mohd Zaheen Hassan. "Synthesis and antimicrobial activity of aryldiazenyl/arylhydrazono pyrazoles." Journal of Chemical Research 45, no. 11-12 (November 2021): 1093–99. http://dx.doi.org/10.1177/17475198211057461.
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 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 джерелаEl-Naggar, Mohamed, Amira S. Abd El-All, Shweekar I. A. El-Naem, Mohamed M. Abdalla та Huda R. M. Rashdan. "New Potent 5α- Reductase and Aromatase Inhibitors Derived from 1,2,3-Triazole Derivative". Molecules 25, № 3 (5 лютого 2020): 672. http://dx.doi.org/10.3390/molecules25030672.
Повний текст джерелаUrbonavičius, Arminas, Graziana Fortunato, Emilija Ambrazaitytė, Elena Plytninkienė, Aurimas Bieliauskas, Vaida Milišiūnaitė, Renzo Luisi, Eglė Arbačiauskienė, Sonata Krikštolaitytė, and Algirdas Šačkus. "Synthesis and Characterization of Novel Heterocyclic Chalcones from 1-Phenyl-1H-pyrazol-3-ol." Molecules 27, no. 12 (June 10, 2022): 3752. http://dx.doi.org/10.3390/molecules27123752.
Повний текст джерелаAtiya, Rana N., Zahraa L. Razzaq, Widad I. Yahya, and Helen M. Neamah. "Synthesis, Characterization and Studying Biological Activity of Heterocyclic Compounds." INTERNATIONAL JOURNAL OF DRUG DELIVERY TECHNOLOGY 13, no. 01 (March 25, 2023): 205–11. http://dx.doi.org/10.25258/ijddt.13.1.31.
Повний текст джерелаMatulevičiūtė, Gita, Eglė Arbačiauskienė, Neringa Kleizienė, Vilija Kederienė, Greta Ragaitė, Miglė Dagilienė, Aurimas Bieliauskas, Vaida Milišiūnaitė, Frank Sløk, and Algirdas Šačkus. "Synthesis and Characterization of Novel Methyl (3)5-(N-Boc-piperidinyl)-1H-pyrazole-4-carboxylates." Molecules 26, no. 13 (June 22, 2021): 3808. http://dx.doi.org/10.3390/molecules26133808.
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