Статті в журналах з теми "Phenyl-derivative"
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Collins, David J., Timothy C. Hughes, and Wynona M. Johnson. "Dihydro-1,2,4-triazin-6(1H)-ones. III. Oxidation Products of 1-Methyl-3-phenyl- 4,5-dihydro-1,2,4-triazin-6(1H)-one." Australian Journal of Chemistry 52, no. 10 (1999): 971. http://dx.doi.org/10.1071/ch99047.
Повний текст джерелаNardis, Sara, Daniel O. Cicero, Silvia Licoccia, Giuseppe Pomarico, Beatrice Berionni Berna, Marco Sette, Giampaolo Ricciardi, et al. "Phenyl Derivative of Iron 5,10,15-Tritolylcorrole." Inorganic Chemistry 53, no. 8 (April 3, 2014): 4215–27. http://dx.doi.org/10.1021/ic5003572.
Повний текст джерелаSaxena, N., S. Kumar, M. K. Sharma, and S. P. Mathur. "Corrosion Inhibition of Mild Steel in Nitric Acid Media by some Schiff Bases Derived from Anisalidine." Polish Journal of Chemical Technology 15, no. 1 (March 1, 2013): 61–67. http://dx.doi.org/10.2478/pjct-2013-0011.
Повний текст джерелаKrečmerová, Marcela, Hubert Hřebabecký, Milena Masojídková, and Antonín Holý. "Synthesis of 5-Phenyl-2(1H)-pyrimidinone Nucleosides." Collection of Czechoslovak Chemical Communications 61, no. 3 (1996): 458–77. http://dx.doi.org/10.1135/cccc19960458.
Повний текст джерелаZhang, Yu-yang, Jian-Ting Pan, and Jian-Yan Huang. "4-{Phenyl[4-(6-phenyl-2,2′-bipyridin-4-yl)phenyl]amino}benzaldehyde." Acta Crystallographica Section E Structure Reports Online 70, no. 8 (July 2, 2014): o840. http://dx.doi.org/10.1107/s1600536814013361.
Повний текст джерелаBöhm, Stanislav, Richard Kubík, Martin Hradilek, Jan Němeček, Michal Hušák, Bohumil Kratochvíl, and Josef Kuthan. "Sterically Crowded Heterocycles. II. Conformational Structure of 2-Phenyl-3-[(Z)-1,3-diphenyl-3-oxopropenyl]imidazo[1,2-a]pyridine and Related Compounds." Collection of Czechoslovak Chemical Communications 60, no. 1 (1995): 115–26. http://dx.doi.org/10.1135/cccc19950115.
Повний текст джерелаKonečný, Václav, Jozefína Žúžiová, Štefan Kováč, and Tibor Liptaj. "Synthesis of Novel 4-Amino-5-(disubstituted amino)-2-phenyl-2H-pyridazin-3-ones." Collection of Czechoslovak Chemical Communications 62, no. 5 (1997): 800–808. http://dx.doi.org/10.1135/cccc19970800.
Повний текст джерелаMistry, Rakesh N., and K. R. Desai. "Studies on Synthesis of Some Novel Heterocyclic Chalcone, Pyrazoline, Pyrimidine - 2 - One, Pyrimidine - 2 - Thione,para-Acetanilide Sulphonyl and Benzoyl Derivatives and their Antimicrobial Activity." E-Journal of Chemistry 2, no. 1 (2005): 30–41. http://dx.doi.org/10.1155/2005/953107.
Повний текст джерелаKhalifa, Nagy M., Ahmed M. Naglah, Mohamed A. Al-Omara, and Abd El-Galil E. Amr. "Synthesis and Reactions of New Chiral Linear Dipeptide Candidates Using Nalidixic Acid as Starting Material." Zeitschrift für Naturforschung B 69, no. 6 (June 1, 2014): 728–36. http://dx.doi.org/10.5560/znb.2014-4031.
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 джерелаIONITA, Petre. "Synthesis and characterization of a new hydrazyl free radical, a formyl-derivative of DPPH." Revue Roumaine de Chimie 66, no. 2 (2021): 205–9. http://dx.doi.org/10.33224/rrch.2021.66.2.12.
Повний текст джерелаNiemevz, Fernando, and Graciela Y. Buldain. "Phenyl biliverdin isomers obtained by chemical oxidation of iron(III) complex of 5-phenyl protoporphyrin IX." Journal of Porphyrins and Phthalocyanines 08, no. 07 (July 2004): 989–95. http://dx.doi.org/10.1142/s1088424604000350.
Повний текст джерелаRosilawati, Ila, Jumina Jumina, and M. Muchalal. "A STUDY OF THE SYNTHESIS OF VERATRYL CYANIDE REQUIRED AS AN INTERMEDIATE FOR THE PREPARATION OF C-9154 ANTIBIOTIC DERIVATIVE FROM VANILIN." Indonesian Journal of Chemistry 2, no. 2 (June 8, 2010): 125–29. http://dx.doi.org/10.22146/ijc.21925.
Повний текст джерелаNahlé, A., R. Salim, F. El Hajjaji, M. R. Aouad, M. Messali, E. Ech-chihbi, B. Hammouti, and M. Taleb. "Novel triazole derivatives as ecological corrosion inhibitors for mild steel in 1.0 M HCl: experimental & theoretical approach." RSC Advances 11, no. 7 (2021): 4147–62. http://dx.doi.org/10.1039/d0ra09679b.
Повний текст джерелаHishmat, O. H., S. S. Mabrouk, A. M. M. Nasef, N. M. A. Shayeb, and S. A. Ismail. "Derivatives of Khellinonequinone and their Aflatoxigenic Activity." Zeitschrift für Naturforschung B 43, no. 3 (March 1, 1988): 343–46. http://dx.doi.org/10.1515/znb-1988-0318.
Повний текст джерелаHuppatz, JL. "Systemic Fungicides. The Synthesis of Pyrazolo[1,5-a]pyrimidine Analogues of Carboxin." Australian Journal of Chemistry 38, no. 1 (1985): 221. http://dx.doi.org/10.1071/ch9850221.
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 джерелаCollins, David J., Timothy C. Hughes, and Wynona M. Johnson. "Dihydro-1,2,4-triazin-6(1H)-ones. II Synthesis of Several Methylated 3-Phenyl- 4,5-dihydro-1,2,4-triazin-6(1H)-ones." Australian Journal of Chemistry 52, no. 5 (1999): 379. http://dx.doi.org/10.1071/ch99012.
Повний текст джерелаClapham, Margaret L., and Christopher J. Douglas. "Two new cases of polymorphism in diagonally substituted rubrene derivatives." Acta Crystallographica Section E Crystallographic Communications 79, no. 4 (March 31, 2023): 406–9. http://dx.doi.org/10.1107/s2056989023002736.
Повний текст джерелаČervinka, Otakar, Václav Dudek, Anna Fábryová, Jiří Kolář, Juraj Lukáč, Jan Šimon, and Martin Viktorin. "Stereoselective synthesis of (±)-threo-2-amino-1-(4-nitrophenyl)-1,3-propanediol." Collection of Czechoslovak Chemical Communications 54, no. 10 (1989): 2748–52. http://dx.doi.org/10.1135/cccc19892748.
Повний текст джерелаTong, Fei, Daichi Kitagawa, Xinning Dong, Seiya Kobatake, and Christopher J. Bardeen. "Photomechanical motion of diarylethene molecular crystal nanowires." Nanoscale 10, no. 7 (2018): 3393–98. http://dx.doi.org/10.1039/c7nr09571f.
Повний текст джерелаBuchta, Vladimír, Milan Pour, Petra Kubanová, Luis Silva, Ivan Votruba, Marie Vopršálová, Radan Schiller, Helena Fáková, and Marcel Špulák. "In Vitro Activities of 3-(Halogenated Phenyl)-5-Acyloxymethyl- 2,5-Dihydrofuran-2-ones against Common and Emerging Yeasts and Molds." Antimicrobial Agents and Chemotherapy 48, no. 3 (March 2004): 873–78. http://dx.doi.org/10.1128/aac.48.3.873-878.2004.
Повний текст джерелаAbdel-Aziz, Hatem A., Hazem A. Ghabbour, Suchada Chantrapromma, and Hoong-Kun Fun. "3-Acetyl-5-phenyl-1-p-tolyl-1H-pyrazole-4-carbonitrile." Acta Crystallographica Section E Structure Reports Online 68, no. 4 (March 24, 2012): o1167. http://dx.doi.org/10.1107/s1600536812011762.
Повний текст джерелаHřebabecký, Hubert, and Jiří Beránek. "Preparation of ribosyl derivatives of 1,2,4-triazol-3(2H)-one and 5-methyl-1,2,4-triazol-3(2H)-one." Collection of Czechoslovak Chemical Communications 50, no. 3 (1985): 779–88. http://dx.doi.org/10.1135/cccc19850779.
Повний текст джерелаRahman Badal, Md Mizanur, Md Tarikul Islam, Reshma Parvin, Md Abul Khaer Morol, Md Maniruzzaman, Mohammad Abu Yousuf, and Md Ershad Halim. "Antimicrobial, Structure-Activity Relationship and Computational Studies of Some Synthesized Chalcone Derivatives." Asian Journal of Chemistry 33, no. 3 (2021): 644–50. http://dx.doi.org/10.14233/ajchem.2021.23028.
Повний текст джерелаHadanu, Ruslin, Mustofa Mustofa, and Nazudin Nazudin. "Synthesis and Antimalarial Activity of 2-Phenyl-1,10-Phenanthroline Derivative Compounds." Jurnal Natur Indonesia 15, no. 1 (July 14, 2014): 57. http://dx.doi.org/10.31258/jnat.15.1.57-62.
Повний текст джерелаFu, Zheng, Long Hua Chen, Sheng Jun Li, and Chao Yuan. "Polymerization and Characterization of N-[o-(4-phenyl-4,5-dihydro-1,3-oxazol-2-yl)phenyl] Methacrylamide." Applied Mechanics and Materials 536-537 (April 2014): 1443–46. http://dx.doi.org/10.4028/www.scientific.net/amm.536-537.1443.
Повний текст джерелаNishimura, Takahiro, Ryota Yabe, and Yusuke Ebe. "Iridium-Catalyzed Direct C–H Allylation of Ketimines." Synthesis 53, no. 17 (April 8, 2021): 3051–56. http://dx.doi.org/10.1055/a-1477-7059.
Повний текст джерелаMoreno-Fuquen, Rodolfo, Juan C. Castillo, Rodrigo Abonia, Javier Ellena, and Juan C. Tenorio. "3-(Diphenylamino)isobenzofuran-1(3H)-one." Acta Crystallographica Section E Structure Reports Online 70, no. 4 (March 29, 2014): o490. http://dx.doi.org/10.1107/s1600536814006266.
Повний текст джерелаZabiulla, S. Naveen, A. Bushra Begum, Shaukath Ara Khanum, and N. K. Lokanath. "Structural studies of a novel bioactive benzophenone derivative: (4-Chloro-2-hydroxy-phenyl)-phenyl-methanone." Molecular Crystals and Liquid Crystals 625, no. 1 (January 22, 2016): 233–37. http://dx.doi.org/10.1080/15421406.2015.1069470.
Повний текст джерелаChung, Yao-Hsien, Lei Sheng, Xing Xing, Lingling Zheng, Mengying Bian, Zhijian Chen, Lixin Xiao, and Qihuang Gong. "A pure blue emitter (CIEy ≈ 0.08) of chrysene derivative with high thermal stability for OLED." Journal of Materials Chemistry C 3, no. 8 (2015): 1794–98. http://dx.doi.org/10.1039/c4tc02669a.
Повний текст джерелаSundaresan, K., V. Priyadarshini, and K. Tharini. "Synthesis, characterization and thrombolytic activity of n-benzyl piperidin 4-one phenyl hydrazone." Journal of Drug Delivery and Therapeutics 9, no. 2 (March 15, 2019): 180–82. http://dx.doi.org/10.22270/jddt.v9i2.2393.
Повний текст джерелаRaghuvarman, B., R. Sivakumar, K. Gokula Krishnan, V. Thanikachalam, and S. Aravindhan. "(E)-1,3-Dimethyl-2,6-diphenylpiperidin-4-oneO-(phenoxycarbonyl)oxime." Acta Crystallographica Section E Structure Reports Online 70, no. 6 (May 24, 2014): o713. http://dx.doi.org/10.1107/s1600536814010526.
Повний текст джерелаJiang, Rong, Shuang Wang, and Jinping Li. "Cucurbit[7]uril–tetraphenylethene host–guest system induced emission activity." RSC Advances 6, no. 6 (2016): 4478–82. http://dx.doi.org/10.1039/c5ra24264a.
Повний текст джерелаGuillon, Jean, Solène Savrimoutou, Sandra Rubio, Stéphane Moreau, Noël Pinaud, Mathieu Marchivie, and Vanessa Desplat. "1-Phenyl-8-[[4-(pyrrolo[1,2-a]quinoxalin-4-yl)phenyl]methyl]-1,3,8-triazaspiro[4.5]decan-4-one: Synthesis, Crystal Structure and Anti-Leukemic Activity." Molbank 2020, no. 1 (January 29, 2020): M1113. http://dx.doi.org/10.3390/m1113.
Повний текст джерелаLiu, Xin-Hua, Bao-An Song, Pinaki S. Bhadury, Hai-Liang Zhu, Ping Cui, Ke-Ke Hou, and Hong-Li Xu. "Novel 5-(3-(Substituted)-4,5-dihydroisoxazol-5-yl)-2-methoxyphenyl Derivatives: Synthesis and Anticancer Activity." Australian Journal of Chemistry 61, no. 11 (2008): 864. http://dx.doi.org/10.1071/ch07395.
Повний текст джерелаRichter, C., C. Schneider, M. T. Quick, P. Volz, R. Mahrwald, J. Hughes, B. Dick, U. Alexiev, and N. P. Ernsting. "Dual-fluorescence pH probe for bio-labelling." Physical Chemistry Chemical Physics 17, no. 45 (2015): 30590–97. http://dx.doi.org/10.1039/c5cp05454k.
Повний текст джерелаGopa, N., E. Porchezhian, and G. V. S. Rama Sarma. "ANALGESIC AND ANTI-INFLAMMATORY ACTIVITIES OF 2-PHENYL (6, 8-DISUBSTITUTED 3,4-DIHYDRO-4-OXOQUINAZLIN-3-YCL) ACETO ACETAMIDES AND THEIR ß (4-SUBSTITUTED PHENYL) AZO ANALOGS." Scientia Pharmaceutica 69, no. 1 (March 30, 2001): 27–32. http://dx.doi.org/10.3797/scipharm.aut-01-04.
Повний текст джерелаŠimo, Ondrej, Alfonz Rybár, and Juraj Alföldi. "Synthesis of 4-Alkyl- or 4-Phenyl-7-methyl-1,2-dihydro-7H-imidazo[1,2,3-cd]purine-6,8-diones." Collection of Czechoslovak Chemical Communications 63, no. 3 (1998): 407–15. http://dx.doi.org/10.1135/cccc19980407.
Повний текст джерелаZhao, Yanfei, Matthias Georg Schwab, Adam Kiersnowski, Wojciech Pisula, Martin Baumgarten, Long Chen, Klaus Müllen, and Chen Li. "Trifluoromethyl-functionalized bathocuproine for polymer solar cells." Journal of Materials Chemistry C 4, no. 21 (2016): 4640–46. http://dx.doi.org/10.1039/c6tc00780e.
Повний текст джерелаVarghese, Beena, Saleh N. Al-Busafi, Fakhr Eldin O. Suliman, and Salma Al-Kindy. "Study on the Reactivity of Amino Acid Chemosensor, NPFNP, with Ethanol: Structural Elucidation through Single Crystal XRD and DFT Calculations." Sultan Qaboos University Journal for Science [SQUJS] 22, no. 1 (January 1, 2017): 16. http://dx.doi.org/10.24200/squjs.vol22iss1pp16-28.
Повний текст джерелаArslan, Tayfun, Zekeriya Biyiklioglu, and Murat Şentürk. "The synthesis of axially disubstituted silicon phthalocyanines, their quaternized derivatives and first inhibitory effect on human cytosolic carbonic anhydrase isozymes hCA I and II." RSC Advances 8, no. 19 (2018): 10172–78. http://dx.doi.org/10.1039/c7ra13674a.
Повний текст джерелаJacobsen, NW, and SE Rose. "1,2,4-Triazines. II. New Zwitterionic Methylation Products of Some 1,2,4-Triazin-5(2H)-Ones and Their Identification by Carbon-13 Nuclear Magnetic Resonance Spectroscopy." Australian Journal of Chemistry 40, no. 5 (1987): 967. http://dx.doi.org/10.1071/ch9870967.
Повний текст джерелаSalem, Marwa S., Rasha A. Hussein, and Wael M. El-Sayed. "Substitution at Phenyl Rings of Chalcone and Schiff Base Moieties Accounts for their Antiproliferative Activity." Anti-Cancer Agents in Medicinal Chemistry 19, no. 5 (June 27, 2019): 620–26. http://dx.doi.org/10.2174/1871520619666190225122338.
Повний текст джерелаMann, Garima, K. Ganesh Kadiyala, M. Thirumal, Anjani Kumar Tiwari, and Anupama Datta. "Receptor mapping using methoxy phenyl piperazine derivative: Preclinical PET imaging." Bioorganic Chemistry 117 (December 2021): 105429. http://dx.doi.org/10.1016/j.bioorg.2021.105429.
Повний текст джерелаMann, Garima, K. Ganesh Kadiyala, M. Thirumal, Anjani Kumar Tiwari, and Anupama Datta. "Receptor mapping using methoxy phenyl piperazine derivative: Preclinical PET imaging." Bioorganic Chemistry 117 (December 2021): 105429. http://dx.doi.org/10.1016/j.bioorg.2021.105429.
Повний текст джерелаIino, Hiroaki, and Jun-Ichi Hanna. "Liquid crystal and crystal structures of a phenyl-benzothienobenzothiophene derivative." Molecular Crystals and Liquid Crystals 647, no. 1 (April 13, 2017): 37–43. http://dx.doi.org/10.1080/15421406.2017.1289427.
Повний текст джерелаStakhira, P., S. Khomyak, V. Cherpak, D. Volyniuk, J. Simokaitiene, A. Tomkeviciene, N. A. Kukhta, et al. "Blue organic light-emitting diodes based on pyrazoline phenyl derivative." Synthetic Metals 162, no. 3-4 (March 2012): 352–55. http://dx.doi.org/10.1016/j.synthmet.2011.12.017.
Повний текст джерелаMazumder, Kishor, Md Emran Hossain, Asma Aktar, Mohammad Mohiuddin, Kishore Kumar Sarkar, Biswajit Biswas, Md Abdullah Aziz, Md Ahsan Abid, and Koichi Fukase. "In Silico Analysis and Experimental Evaluation of Ester Prodrugs of Ketoprofen for Oral Delivery: With a View to Reduce Toxicity." Processes 9, no. 12 (December 9, 2021): 2221. http://dx.doi.org/10.3390/pr9122221.
Повний текст джерелаFun, Hoong-Kun, Suchada Chantrapromma, Weerawat Sripet, Pumsak Ruanwas, and Nawong Boonnak. "4-Bromo-N-phenylbenzamide." Acta Crystallographica Section E Structure Reports Online 68, no. 4 (March 31, 2012): o1269—o1270. http://dx.doi.org/10.1107/s1600536812013487.
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