Статті в журналах з теми "Aryl Compounds"
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Wang, Xi-Cun, Fang Wang, Zheng-Jun Quan, Man-Gang Wang, and Zheng Li. "An efficient and clean synthesis of 1-aroyl-3-aryl-4-substituted imidazole-2-thiones in water." Journal of Chemical Research 2005, no. 11 (November 2005): 689–90. http://dx.doi.org/10.3184/030823405774909423.
Повний текст джерелаKrutošíková, Alžbeta, Miloslava Dandárová, and Juraj Alföldi. "5-Aryl-2-furancarbaldehyde Hydrazones and Related Compounds." Collection of Czechoslovak Chemical Communications 58, no. 8 (1993): 1905–13. http://dx.doi.org/10.1135/cccc19931905.
Повний текст джерелаSoni, Love Kumar, Tamanna Narsinghani, and Rica Jain. "Synthesis and Antibacterial Screening of Some 1-Aroyl-3-aryl Thiourea Derivatives." ISRN Medicinal Chemistry 2014 (January 29, 2014): 1–6. http://dx.doi.org/10.1155/2014/393102.
Повний текст джерелаKalam, Sirisha, Rajyalaxmi I, and Olivia S. "Synthesis and In vitro P-Glycoprotein Inhibitory Activity of Novel 1,4-Dihydropyridine Derivatives." International Journal of Pharmaceutical Sciences and Nanotechnology 7, no. 3 (August 31, 2014): 2544–52. http://dx.doi.org/10.37285/ijpsn.2014.7.3.6.
Повний текст джерелаRaval, J. P., and K. R. Desai. "Synthesis of 3-Phenyl-4[4-(m-nitrophenyl)-N-2-(2’-arylureido / arylthioureido-4’-N-morpholino-s-triazin)-benzo-[6,7]-coumarins and their Applicatiions." E-Journal of Chemistry 1, no. 5 (2004): 211–15. http://dx.doi.org/10.1155/2004/873425.
Повний текст джерелаKudalkar, Gaurav P., Virendra K. Tiwari, Joshua D. Lee, and David B. Berkowitz. "A Hammett Study of Clostridium acetobutylicum Alcohol Dehydrogenase (CaADH): An Enzyme with Remarkable Substrate Promiscuity and Utility for Organic Synthesis." Synlett 31, no. 03 (January 16, 2020): 237–47. http://dx.doi.org/10.1055/s-0039-1691576.
Повний текст джерелаChandra, Priyanka, Swastika Ganguly, Rajdeep Dey, and Biswatrish Sarkar. "Synthesis, antibacterial activities, binding mode analysis and predictive ADME studies of novel 1-(aryl)-2-(1H-imidazol-1-yl)methanones." INTERNATIONAL JOURNAL OF PHARMACEUTICAL EDUCATION AND RESEARCH (IJPER) 2, no. 02 (December 30, 2020): 39–45. http://dx.doi.org/10.37021/ijper.v2i2.2.
Повний текст джерелаChandra, Priyanka, Swastika Ganguly, Rajdeep Dey, and Biswatrish Sarkar. "Synthesis, antibacterial activities, binding mode analysis and predictive ADME studies of novel 1-(aryl)-2-(1H-imidazol-1-yl)methanones." INTERNATIONAL JOURNAL OF PHARMACEUTICAL EDUCATION AND RESEARCH (IJPER) 2, no. 02 (December 30, 2020): 39–45. http://dx.doi.org/10.37021/ijper.v2i2.2.
Повний текст джерелаWang, Lizhong, Zhenjie Su, Siran Qian, Weijian Ye, and Cunde Wang. "Efficient Preparation of 2,3-Disubstituted Cyclopropane-1-Carbonitriles via Selective Decarboxylation of 1-Cyanocyclopropane-1-Carboxylates." Journal of Chemical Research 41, no. 11 (November 2017): 636–40. http://dx.doi.org/10.3184/174751917x15094552081161.
Повний текст джерелаUtri, Gerhard, Karl-Eberhard Schwarzhans, and Günter M. Allmaier. "Ferrocenyl-aryl-plumbane / Ferrocenyl-aryl-plumbanes." Zeitschrift für Naturforschung B 45, no. 6 (June 1, 1990): 755–62. http://dx.doi.org/10.1515/znb-1990-0606.
Повний текст джерелаGudimani, Parashuram, Samundeeswari Lokesh Shastri, Varsha Pawar, Nagashree Uday Hebbar, Lokesh Anand Shastri, Shrinivas Joshi, Shyam Kumar Vootla, Sheela Khanapure, and Vinay Sunagar. "Synthesis, molecular docking, and biological evaluation of methyl-5-(hydroxyimino)-3-(aryl-substituted)hexanoate derivatives." European Journal of Chemistry 13, no. 2 (June 30, 2022): 151–61. http://dx.doi.org/10.5155/eurjchem.13.2.151-161.2220.
Повний текст джерелаMasri, Abdulkader, Ayaz Anwar, Naveed Ahmed Khan, Muhammad Saquib Shahbaz, Khalid Mohammed Khan, Syed Shahabuddin, and Ruqaiyyah Siddiqui. "Antibacterial Effects of Quinazolin-4(3H)-One Functionalized-Conjugated Silver Nanoparticles." Antibiotics 8, no. 4 (October 9, 2019): 179. http://dx.doi.org/10.3390/antibiotics8040179.
Повний текст джерелаLan, Jihong, Rongxiang Chen, Fangfang Duo, Menghui Hu, and Xiaoyan Lu. "Visible-Light Photocatalytic Reduction of Aryl Halides as a Source of Aryl Radicals." Molecules 27, no. 17 (August 23, 2022): 5364. http://dx.doi.org/10.3390/molecules27175364.
Повний текст джерелаGoyal, Anju, and Sandeep Jain. "Syntheses and Antibacterial Studies of Some 1-Phenyl-3-(4-(2-ethanoloxy) phenyl)-5-aryl-1H-pyrazoles." Journal of Chemistry 2013 (2013): 1–5. http://dx.doi.org/10.1155/2013/950491.
Повний текст джерелаFROHN, H. J. "ChemInform Abstract: Aryl-Xenon Compounds." ChemInform 25, no. 6 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199406285.
Повний текст джерелаAl-Khazragie, Zainab K., Bushra K. Al-Salami та Adnan J. M. Al-Fartosy. "Synthesis, Characterization, and Antioxidant, Antimicrobial and Toxic Properties of Novel Δ2 -1,3,4-thiadiazoline and Δ2 -1,3,4-selenadiazoline Derivatives". INTERNATIONAL JOURNAL OF DRUG DELIVERY TECHNOLOGY 12, № 01 (25 червня 2022): 113–26. http://dx.doi.org/10.25258/ijddt.12.1.22.
Повний текст джерелаMete, Ebru, Halise Inci Gul, Pakize Canturk, Zeki Topcu, Bulbul Pandit, Mustafa Gul, and Pui-Kai Li. "Biological Activity of 1-Aryl-3-phenethylamino-1-propanone Hydrochlorides and 3-Aroyl-4-aryl-1-phenethyl-4-piperidinols on PC-3 Cells and DNA Topoisomerase I Enzyme." Zeitschrift für Naturforschung C 65, no. 11-12 (December 1, 2010): 647–52. http://dx.doi.org/10.1515/znc-2010-11-1203.
Повний текст джерелаLittle, Vanessa Renee, and Keith Vaughan. "Synthesis and characterization of several series of 4-acyl-1-[2-aryl-1-diazenyl]piperazines." Canadian Journal of Chemistry 92, no. 9 (September 2014): 838–48. http://dx.doi.org/10.1139/cjc-2014-0242.
Повний текст джерелаOgorodnik, A. G., V. A. Yanchenko, L. S. Bobkova, N. M. Seredinska та A. M. Demchenko. "Synthesis and anаlgеsic activity 5-methyl-3-aryl[1,2,4]triazolo[4,3-a]pyrimidin-7-oles derivatives". Farmatsevtychnyi zhurnal, № 2 (14 серпня 2018): 55–61. http://dx.doi.org/10.32352/0367-3057.2.17.07.
Повний текст джерелаPeeters, Elien, Geert Hooyberghs, Stijn Robijns, Kai Waldrant, Ami De Weerdt, Nicolas Delattin, Veerle Liebens, et al. "Modulation of the Substitution Pattern of 5-Aryl-2-Aminoimidazoles Allows Fine-Tuning of Their Antibiofilm Activity Spectrum and Toxicity." Antimicrobial Agents and Chemotherapy 60, no. 11 (August 22, 2016): 6483–97. http://dx.doi.org/10.1128/aac.00035-16.
Повний текст джерелаRaied, Mustafa Shakir, Abed Saoud Shaimaa, Faruk Hussain Dhuha, Fahad Ali Khalid, Shawqi Algburi Firas, and Salman Jasim Husam. "Synthesis, Antioxidant ability and Docking study for new 4,4'-((2-(Aryl)-1H-benzo[d]imidazole-1,3(2H)-diyl)bis(methylene))diphenol)." Research Journal of Chemistry and Environment 26, no. 10 (September 25, 2022): 28–36. http://dx.doi.org/10.25303/2610rjce028036.
Повний текст джерелаNancy, Sakshi Chaudhary, Deepak Kumar, and Archana. "Synthesis and Anti-inflammatory Activity of Newer Indolyl Pyrazolines and Indolyl Isoxazolines." Asian Journal of Organic & Medicinal Chemistry 7, no. 1 (2022): 79–83. http://dx.doi.org/10.14233/ajomc.2022.ajomc-p365.
Повний текст джерелаRawat, Bhupender Singh, and S. C. Mehra. "SYNTHESIS OF SOME NEW 1, 3-DI METHYL SUBSTITUTED GUANIDINE WITH POSSIBLE ANTIBACTERIAL AND ANTIFUNGAL ACTIVITY." Green Chemistry & Technology Letters 2, no. 3 (June 26, 2016): 138–40. http://dx.doi.org/10.18510/gctl.2016.233.
Повний текст джерелаAdachi, Ryutaro, Tsuyoshi Ishii, Shinichi Matsumoto, Takuya Satou, Junichi Sakamoto, and Tomohiro Kawamoto. "Discovery of Human Intestinal MGAT Inhibitors Using High-Throughput Mass Spectrometry." SLAS DISCOVERY: Advancing the Science of Drug Discovery 22, no. 4 (October 8, 2016): 360–65. http://dx.doi.org/10.1177/1087057116673181.
Повний текст джерелаYao, Yun-Xin, Nan-Nan Jia, Ya-Nan Cao, Xing-Xiu Chen, Feng Gao, and Xiao-Xia Liang. "Copper-Catalyzed Synthesis, Bio-Evaluation, and in Silico Studies of 2-Aryl-N-alkylbenzimidazoles as Neuroprotective Agents." Catalysts 8, no. 10 (September 30, 2018): 433. http://dx.doi.org/10.3390/catal8100433.
Повний текст джерелаSingh, A. "SYNTHESIS OF NOVEL QUINAZOLIN-4(3H)-ONYL AZETIDINONES AS POTENTIAL ANTICONVULSANT AGENTS." INDIAN DRUGS 54, no. 11 (November 28, 2017): 22–27. http://dx.doi.org/10.53879/id.54.11.10766.
Повний текст джерелаJaradat, Nidal, Mohammed Hawash, and Murad Abualhasan. "Synthesis and Biological Evaluation of Benzodioxol Derivatives as Cyclooxygenase Inhibitors." Letters in Drug Design & Discovery 17, no. 9 (September 11, 2020): 1117–25. http://dx.doi.org/10.2174/1570180817999200420114402.
Повний текст джерелаHeidari, Alireza. "Interaction between Cadmium Oxide (CdO) Nanoparticles Aggregation Linked to DNA/RNA and Aryl Mercaptanes With Various Chain Length." Academic Journal of Chemistry, no. 72 (April 28, 2022): 23–29. http://dx.doi.org/10.32861/ajc.72.23.29.
Повний текст джерелаWanare, Rajendra K., Yogesh V. Punatkar, and Ravin M. Jugade. "SYNTHESIS, POLAROGRAPHIC AND ANTIMICROBIAL STUDIES OF BENZISOXAZOLYLN- GLUCOSIDES." Journal of Advanced Scientific Research 12, no. 04 Suppl 1 (December 31, 2021): 281–87. http://dx.doi.org/10.55218/jasr.s1202112432.
Повний текст джерелаBhat, Mashooq Ahmad, Ahmad M. Naglah, Azmat Ali Khan, and Abdullah Al-Dhfyan. "Synthesis, molecular modelling and antibacterial activity of 4-aryl-thiosemicarbazides." Polish Journal of Chemical Technology 24, no. 1 (March 1, 2022): 39–46. http://dx.doi.org/10.2478/pjct-2022-0006.
Повний текст джерелаHeidari, Alireza. "Biomedical and Biochemical Approaches and Strategies for Targeting and Delivery of Cadmium Oxide (CdO) Nanoparticles Aggregation Linked to DNA/RNA by Aryl Mercaptanes with Various Chain Length." Biomedicine and Chemical Sciences 1, no. 4 (October 1, 2022): 215–24. http://dx.doi.org/10.48112/bcs.v1i4.149.
Повний текст джерелаHeidari, Alireza. "A New Viewpoint and Outlook on Aryl Mercaptans as Strong Nucleophiles with Various Chain Length Linked to DNA/RNA and Cadmium Oxide (CdO) Nanoparticles Sandwiched Complex." Asian Journal of Engineering and Applied Technology 10, no. 2 (November 5, 2021): 34–38. http://dx.doi.org/10.51983/ajeat-2021.10.2.3073.
Повний текст джерелаClaridge, Robert P., Ross W. Millar, John P. B. Sandall, and Claire Thompson. "Preparation of a Series of N-Aryl-S,S-diphenylsulfilimines by Nucleophilic Attack of S,S-Diphenyl-sulfilimine on Activated Halogenoaromatic Compounds." Journal of Chemical Research 23, no. 8 (August 1999): 520. http://dx.doi.org/10.1177/174751989902300833.
Повний текст джерелаAshok, D., and K. Aravind. "Microwave Assisted Synthesis of New 1-{2, 4-Dihydroxy-5-[5-(aryl)-1-pyridine/pyrimidine-4-carbonyl)-4, 5-dihydro-1H-pyrazol-3-yl]-phenyl}-3-(aryl)-propenones and their Antibacterial Activity." E-Journal of Chemistry 6, no. 2 (2009): 323–31. http://dx.doi.org/10.1155/2009/982746.
Повний текст джерелаMa, Shuchao, Ben Ouyang, Linan Wang, and Lei Yao. "Design and Biological Evaluation of 3-Aryl-4-alkylpyrazol-5-amines Based on the Target Fishing." Current Computer-Aided Drug Design 16, no. 5 (November 9, 2020): 564–70. http://dx.doi.org/10.2174/1573409915666191003123900.
Повний текст джерелаMacaev, Fliur. "What Can Be Done with the Acetyl Group of Aryl-1-Ethanones?" Chemistry Journal of Moldova 1, no. 1 (December 2006): 36–49. http://dx.doi.org/10.19261/cjm.2006.01(1).10.
Повний текст джерелаNagaki, Aiichiro, and Yosuke Ashikari. "Homogeneous Catalyzed Aryl–Aryl Cross-Couplings in Flow." Synthesis 53, no. 11 (January 18, 2021): 1879–88. http://dx.doi.org/10.1055/a-1360-7798.
Повний текст джерелаKansagara, N. N., V. R. Dangar, and V. R. Shah. "Synthesis, Characterization and Antimicrobial Evaluation of Schiff’s Base and Aryl Aminomethyl Derivatives." International Letters of Chemistry, Physics and Astronomy 64 (February 2016): 89–94. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.64.89.
Повний текст джерелаKansagara, N. N., V. R. Dangar, and V. R. Shah. "Synthesis, Characterization and Antimicrobial Evaluation of Schiff’s Base and Aryl Aminomethyl Derivatives." International Letters of Chemistry, Physics and Astronomy 64 (February 15, 2016): 89–94. http://dx.doi.org/10.56431/p-5z8xff.
Повний текст джерелаLi, Jun, Constantin G. Daniliuc, Gerald Kehr, and Gerhard Erker. "A convenient route to internally phosphane-stabilized aryltriborane(7) compounds." Chemical Communications 54, no. 89 (2018): 12606–9. http://dx.doi.org/10.1039/c8cc06728g.
Повний текст джерелаDrapak, Iryna, Borys Zimenkovsky, Lina Perekhoda, Мargarita Suleyman, Hanna Yeromina, Natalia Skaletska, Natalya Seredynska, and Anatoly Demchenko. "Search for angiotensin II receptor antagonists among 4-aryl-n-(aryl)-3-(prop-2-en-1-yl)-2,3-dihydro-1,3-thiazol-2-imine derivatives." Pharmacia 66, no. 4 (December 31, 2019): 181–86. http://dx.doi.org/10.3897/pharmacia.66.e36808.
Повний текст джерелаMiller-Clark, Lyndsy A., Peter E. Christ, and Tong Ren. "Diruthenium aryl compounds – tuning of electrochemical responses and solubility." Dalton Transactions 51, no. 2 (2022): 580–86. http://dx.doi.org/10.1039/d1dt03957a.
Повний текст джерелаNguyen, Thanh Vinh. "A RESEARCH ON SYNTHESIS OF N-ARYL AZACYCLOALKANE UNDER MICROWAVE IRRADIATION." Journal of Science and Technique 17, no. 4 (September 27, 2022): 14–21. http://dx.doi.org/10.56651/lqdtu.jst.v17.n04.400.
Повний текст джерелаBoyer, Jérémie, Vania Bernardes-Génisson, and Françoise Nepveu. "Access to Unsymmetrical 1,2-Diketone Intermediates via Benzeneseleninic Anhydride-Promoted Oxidation: Application to Indolone-N-Oxide Synthesis." Journal of Chemical Research 2003, no. 8 (August 2003): 507–8. http://dx.doi.org/10.3184/030823403103174731.
Повний текст джерелаLapadatescu, Carmen, Christian Giniès, Jean-Luc Le Quéré, and Pascal Bonnarme. "Novel Scheme for Biosynthesis of Aryl Metabolites from l-Phenylalanine in the FungusBjerkandera adusta." Applied and Environmental Microbiology 66, no. 4 (April 1, 2000): 1517–22. http://dx.doi.org/10.1128/aem.66.4.1517-1522.2000.
Повний текст джерелаBaranano, David, Grace Mann, and John F. Hartwig. "Nickel and Palladium-Catalyzed Cross-Couplings that Form Carbon-Heteroatom and Carbon-Element Bonds." Current Organic Chemistry 1, no. 3 (September 1997): 287–305. http://dx.doi.org/10.2174/1385272801666220124194647.
Повний текст джерелаGribanov, Pavel S., Dmitry A. Loginov, Dmitry A. Lypenko, Artem V. Dmitriev, Sergey I. Pozin, Alexey E. Aleksandrov, Alexey R. Tameev, Igor L. Martynov, Andrey Yu Chernyadyev, and Sergey N. Osipov. "New Unsymmetrically Substituted Benzothiadiazole-Based Luminophores: Synthesis, Optical, Electrochemical Studies, Charge Transport, and Electroluminescent Characteristics." Molecules 26, no. 24 (December 15, 2021): 7596. http://dx.doi.org/10.3390/molecules26247596.
Повний текст джерелаMashweu, Adelaide R., Varsha P. Chhiba-Govindjee, Moira L. Bode, and Dean Brady. "Substrate Profiling of the Cobalt Nitrile Hydratase from Rhodococcus rhodochrous ATCC BAA 870." Molecules 25, no. 1 (January 6, 2020): 238. http://dx.doi.org/10.3390/molecules25010238.
Повний текст джерелаDemchenko, Sergii, Roman Lesyk, Oleh Yadlovskyi, Johannes Zuegg, Alysha G. Elliott, Iryna Drapak, Yuliia Fedchenkova, Zinaida Suvorova, and Anatolii Demchenko. "Synthesis, Antibacterial and Antifungal Activity of New 3-Aryl-5H-pyrrolo[1,2-a]imidazole and 5H-Imidazo[1,2-a]azepine Quaternary Salts." Molecules 26, no. 14 (July 13, 2021): 4253. http://dx.doi.org/10.3390/molecules26144253.
Повний текст джерелаNaveena Kumari, H. M., Manjunath Harihara Mathada, Mahesh Kumar, K. T. Suda, and K. M. Basavaraja. "Synthesis, Characterization, Antimicrobial Screening of 5-Bromobenzofuranyl Aryl Ureas and Carbamates." Asian Journal of Organic & Medicinal Chemistry 4, no. 4 (2019): 232–35. http://dx.doi.org/10.14233/ajomc.2019.ajomc-p215.
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