Статті в журналах з теми "Novel synthesis protocols"
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Voutyritsa, Errika, Ierasia Triandafillidi, Nikolaos V. Tzouras, Nikolaos F. Nikitas, Eleftherios K. Pefkianakis, Georgios C. Vougioukalakis, and Christoforos G. Kokotos. "Photocatalytic Atom Transfer Radical Addition to Olefins Utilizing Novel Photocatalysts." Molecules 24, no. 9 (April 26, 2019): 1644. http://dx.doi.org/10.3390/molecules24091644.
Повний текст джерелаBahou, Calise, Daniel A. Richards, Antoine Maruani, Elizabeth A. Love, Faiza Javaid, Stephen Caddick, James R. Baker, and Vijay Chudasama. "Highly homogeneous antibody modification through optimisation of the synthesis and conjugation of functionalised dibromopyridazinediones." Organic & Biomolecular Chemistry 16, no. 8 (2018): 1359–66. http://dx.doi.org/10.1039/c7ob03138f.
Повний текст джерелаOdaa, M. E., U. C. Okoro, and D. I. Ugwu. "Synthesis of Novel Angular Diazaphenoxazinone Derivatives via Palladium Catalyzed Buchwald-Hartwig Amidation Protocols." Asian Journal of Chemistry 27, no. 8 (2015): 3069–73. http://dx.doi.org/10.14233/ajchem.2015.18874.
Повний текст джерелаChawla, P., Garg P, Panjwani D, and S. A. Saraf. "Synthesis of Some Novel 5-Substituted Arylidene – 2, 4 –Thiazolidinediones as Bioactive Agents." International Journal of Pharmaceutical Sciences and Nanotechnology 4, no. 1 (May 31, 2011): 1373–78. http://dx.doi.org/10.37285/ijpsn.2011.4.1.10.
Повний текст джерелаGenç, Hasan, Volkan Taşdemir, İsrafil Tozlu, and Erdal Ögün. "Synthesis of Novel Tetra-Substituted Pyrazole Derivatives from 2,3- Furandione." Letters in Organic Chemistry 16, no. 11 (October 2, 2019): 891–97. http://dx.doi.org/10.2174/1570178616666190314150302.
Повний текст джерелаSalas-Reyes, V. "Chiral Synthesis of (R)-(-)(5Z)-4-Hydroxy-5-tetradecenoic Acid-4-lactone." Zeitschrift für Naturforschung B 50, no. 10 (October 1, 1995): 1537–42. http://dx.doi.org/10.1515/znb-1995-1018.
Повний текст джерелаHerlekar, Mihir, Siddhivinayak Barve, and Rakesh Kumar. "Plant-Mediated Green Synthesis of Iron Nanoparticles." Journal of Nanoparticles 2014 (October 2, 2014): 1–9. http://dx.doi.org/10.1155/2014/140614.
Повний текст джерелаGadde, Satyanarayana, Yun Cheuk Leung, Mohan Bhadbade, Belamy B. Cheung, David StC Black, and Naresh Kumar. "Synthesis of a Novel Library of 1-Substituted Pyrido[1,2-a]benzimidazoles." Australian Journal of Chemistry 73, no. 12 (2020): 1208. http://dx.doi.org/10.1071/ch20173.
Повний текст джерелаHiroto, Satoru. "Development of synthetic protocols for porphyrins and their analogs based on distorted structures — a SPP/JPP Young Investigator Award paper." Journal of Porphyrins and Phthalocyanines 24, no. 11n12 (October 21, 2020): 1258–71. http://dx.doi.org/10.1142/s1088424620500376.
Повний текст джерелаCai, Qun, Yan-Ping Zhu, Yang Gao, Jing-Jing Sun, and An-Xin Wu. "A direct method for the synthesis of indolizine derivatives from easily available aromatic ketones, pyridines, and acrylonitrile derivatives." Canadian Journal of Chemistry 91, no. 6 (June 2013): 414–19. http://dx.doi.org/10.1139/cjc-2012-0534.
Повний текст джерелаNourine, L., R. Ragab, and F. Toumani. "Decidability and Complexity of Web Service Business Protocol Synthesis." International Journal of Cooperative Information Systems 25, no. 03 (September 2016): 1650008. http://dx.doi.org/10.1142/s0218843016500088.
Повний текст джерелаWildermann, Angela, Yann Foricher, Thomas Netscher, and Werner Bonrath. "New application of indium catalysts: A novel and green concept in the fine chemicals industry." Pure and Applied Chemistry 79, no. 11 (January 1, 2007): 1839–46. http://dx.doi.org/10.1351/pac200779111839.
Повний текст джерелаForchetta, Mattia, Valeria Conte, Giulia Fiorani, Pierluca Galloni та Federica Sabuzi. "A Sustainable Improvement of ω-Bromoalkylphosphonates Synthesis to Access Novel KuQuinones". Organics 2, № 2 (3 червня 2021): 107–17. http://dx.doi.org/10.3390/org2020010.
Повний текст джерелаXu, Li-Wen, and Chun-Gu Xia. "A Catalytic Enantioselective Aza-Michael Reaction: Novel Protocols for Asymmetric Synthesis of ?-Amino Carbonyl Compounds." European Journal of Organic Chemistry 2005, no. 4 (February 2005): 633–39. http://dx.doi.org/10.1002/ejoc.200400619.
Повний текст джерелаUsui, Kenji, Shin-ichiro Yokota, Kazuya Iwata, and Yoshio Hamada. "Novel Purification Process for Amyloid Beta Peptide(1-40)." Processes 8, no. 4 (April 15, 2020): 464. http://dx.doi.org/10.3390/pr8040464.
Повний текст джерелаZhang, Rui, Huaiwei Ding, Xiangling Pu, Zhiping Qian, and Yan Xiao. "Recent Advances in the Synthesis of Sulfides, Sulfoxides and Sulfones via C-S Bond Construction from Non-Halide Substrates." Catalysts 10, no. 11 (November 17, 2020): 1339. http://dx.doi.org/10.3390/catal10111339.
Повний текст джерелаDanishefsky, Samuel J., Harold G. Selnick, David M. Armistead, and Francine E. Wincott. "The total synthesis of avermectin A1a. New protocols for the synthesis of novel 2-deoxypyranose systems and their axial glycosides." Journal of the American Chemical Society 109, no. 26 (December 1987): 8119–20. http://dx.doi.org/10.1021/ja00260a046.
Повний текст джерелаZamora, P. P. Zamora. "Theoretical study of Aniline-Thiophene based Polymers." JOURNAL OF ADVANCES IN CHEMISTRY 6, no. 2 (April 24, 2017): 982–89. http://dx.doi.org/10.24297/jac.v6i2.6582.
Повний текст джерелаAvila-Ortiz, Claudia Gabriela, and Eusebio Juaristi. "Novel Methodologies for Chemical Activation in Organic Synthesis under Solvent-Free Reaction Conditions." Molecules 25, no. 16 (August 6, 2020): 3579. http://dx.doi.org/10.3390/molecules25163579.
Повний текст джерелаBehera, Archanamayee, and Suvarn Kulkarni. "Chemical Synthesis of Rare, Deoxy-Amino Sugars Containing Bacterial Glycoconjugates as Potential Vaccine Candidates." Molecules 23, no. 8 (August 10, 2018): 1997. http://dx.doi.org/10.3390/molecules23081997.
Повний текст джерелаSteingruber, H. Sebastián, Pamela Mendioroz, María A. Volpe, and Darío C. Gerbino. "Direct Arylation-Based Synthesis of Carbazoles Using an Efficient Palladium Nanocatalyst under Microwave Irradiation." Chemistry Proceedings 3, no. 1 (November 14, 2020): 70. http://dx.doi.org/10.3390/ecsoc-24-08314.
Повний текст джерелаÖzil, Musa, Güven Tacal, Nimet Baltaş, and Mustafa Emirik. "Synthesis and Molecular Docking Studies of Novel Triazole Derivatives as Antioxidant Agents." Letters in Organic Chemistry 17, no. 4 (March 25, 2020): 309–20. http://dx.doi.org/10.2174/1570178616666190828200207.
Повний текст джерелаGill, Manjinder, Dinesh Tanwar, and Anjali Ratan. "Facile One-Pot Synthesis of Substituted Hydantoins from Carbamates." Synlett 28, no. 17 (August 3, 2017): 2285–90. http://dx.doi.org/10.1055/s-0036-1588468.
Повний текст джерелаHong. "“Cell-Free Synthetic Biology”: Synthetic Biology Meets Cell-Free Protein Synthesis." Methods and Protocols 2, no. 4 (October 8, 2019): 80. http://dx.doi.org/10.3390/mps2040080.
Повний текст джерелаLusardi, Matteo, Aldo Profumo, Chiara Rotolo, Erika Iervasi, Camillo Rosano, Andrea Spallarossa, and Marco Ponassi. "Regioselective Synthesis, Structural Characterization, and Antiproliferative Activity of Novel Tetra-Substituted Phenylaminopyrazole Derivatives." Molecules 27, no. 18 (September 8, 2022): 5814. http://dx.doi.org/10.3390/molecules27185814.
Повний текст джерелаTurner, Nicholas J. "The Application of Enzymes in the Synthesis of Amino Acids, Peptides and Carbohydrates." Current Organic Chemistry 1, no. 1 (May 1997): 21–36. http://dx.doi.org/10.2174/1385272801666220121183432.
Повний текст джерелаIhnatova, Tetiana, Andriy Kaplaushenko, Yuliia Frolova, and Evheniy Pryhlo. "Synthesis and antioxidant properties of some new 5-phenethyl-3-thio-1,2,4-triazoles." Pharmacia 68, no. 1 (January 8, 2021): 129–33. http://dx.doi.org/10.3897/pharmacia.68.e53320.
Повний текст джерелаIhnatova, Tetiana, Andriy Kaplaushenko, Yuliia Frolova, and Evheniy Pryhlo. "Synthesis and antioxidant properties of some new 5-phenethyl-3-thio-1,2,4-triazoles." Pharmacia 68, no. 1 (January 8, 2021): 129–33. http://dx.doi.org/10.3897/pharmacia.68.e53320.
Повний текст джерелаEdr, Antonín, Dominika Wrobel, Alena Krupková, Lucie Červenková Šťastná, Petra Cuřínová, Aleš Novák, Jan Malý, et al. "Adaptive Synthesis of Functional Amphiphilic Dendrons as a Novel Approach to Artificial Supramolecular Objects." International Journal of Molecular Sciences 23, no. 4 (February 14, 2022): 2114. http://dx.doi.org/10.3390/ijms23042114.
Повний текст джерелаOrlandin, Andrea, Ivan Guryanov, Lucia Ferrazzano, Barbara Biondi, Francesca Biscaglia, Claudia Storti, Marzio Rancan, Fernando Formaggio, Antonio Ricci, and Walter Cabri. "Carbodiimide-Mediated Beckmann Rearrangement of Oxyma-B as a Side Reaction in Peptide Synthesis." Molecules 27, no. 13 (June 30, 2022): 4235. http://dx.doi.org/10.3390/molecules27134235.
Повний текст джерелаAbdelazeem, Ahmed H., Yasser M. A. Mohamed, Ahmed M. Gouda, Hany A. Omar, and Majed M. Al Robaian. "Novel Thymohydroquinone Derivatives as Potential Anticancer Agents: Design, Synthesis, and Biological Screening." Australian Journal of Chemistry 69, no. 11 (2016): 1277. http://dx.doi.org/10.1071/ch16102.
Повний текст джерелаKumar, Amit, Muhammad Omar Shaikh, and Cheng-Hsin Chuang. "Silver Nanowire Synthesis and Strategies for Fabricating Transparent Conducting Electrodes." Nanomaterials 11, no. 3 (March 10, 2021): 693. http://dx.doi.org/10.3390/nano11030693.
Повний текст джерелаBhosale, Rohit Rajendra, A. S. Kulkarni, S. S. Gilda, N. H. Aloorkar, R. A. Osmani, and B. R. Harkare. "Innovative Eco-friendly Approaches for Green Synthesis of Silver Nanoparticles." International Journal of Pharmaceutical Sciences and Nanotechnology 7, no. 1 (February 28, 2014): 2328–37. http://dx.doi.org/10.37285/ijpsn.2014.7.1.3.
Повний текст джерелаSultana, Shameem, and Rangapuram Vasanthi. "Synthesis and Antimicrobial Evaluation of Pyrazole-4-carboxamide Derivatives." Asian Journal of Chemistry 34, no. 9 (2022): 2222–26. http://dx.doi.org/10.14233/ajchem.2022.23834.
Повний текст джерелаEghbali, Paria, Bilal Nişancı, and Önder Metin. "Graphene hydrogel supported palladium nanoparticles as an efficient and reusable heterogeneous catalysts in the transfer hydrogenation of nitroarenes using ammonia borane as a hydrogen source." Pure and Applied Chemistry 90, no. 2 (February 23, 2018): 327–35. http://dx.doi.org/10.1515/pac-2017-0714.
Повний текст джерелаJaved, Salim, Mahipal Bodugam, Jessica Torres, Arghya Ganguly та Paul R. Hanson. "Modular Synthesis of Novel Macrocycles Bearing α,β-Unsaturated Chemotypes through a Series of One-Pot, Sequential Protocols". Chemistry - A European Journal 22, № 20 (5 квітня 2016): 6755–58. http://dx.doi.org/10.1002/chem.201601004.
Повний текст джерелаBozhanova, Nina, Mikhail Baranov, Nadezhda Baleeva, Alexey Gavrikov, and Alexander Mishin. "Red-Shifted Aminated Derivatives of GFP Chromophore for Live-Cell Protein Labeling with Lipocalins." International Journal of Molecular Sciences 19, no. 12 (November 28, 2018): 3778. http://dx.doi.org/10.3390/ijms19123778.
Повний текст джерелаValsami-Jones, E., D. Berhanu, A. Dybowska, S. Misra, A. R. Boccaccini, T. D. Tetley, S. N. Luoma, and J. A. Plant. "Nanomaterial synthesis and characterization for toxicological studies: TiO2 case study." Mineralogical Magazine 72, no. 1 (February 2008): 515–19. http://dx.doi.org/10.1180/minmag.2008.072.1.515.
Повний текст джерелаAbdelazeem, Ahmed H., Yasser M. A. Mohamed, Ahmed M. Gouda, Hany A. Omar, and Majed M. Al Robaian. "Corrigendum to: Novel Thymohydroquinone Derivatives as Potential Anticancer Agents: Design, Synthesis, and Biological Screening." Australian Journal of Chemistry 70, no. 6 (2017): 755. http://dx.doi.org/10.1071/ch16102_co.
Повний текст джерелаGrillo, Alessandro, and Bruno Mattia Bizzarri. "Catalytic Enantioselective Diels Alder Reaction: Application in the Synthesis of Antiviral Agents." Catalysts 12, no. 2 (January 25, 2022): 150. http://dx.doi.org/10.3390/catal12020150.
Повний текст джерелаTaherkhorsand, Hasti, and Mohammad Nikpassand. "One-pot Synthesis of Novel 2-pyrazolo-3-phenyl-1,3-thiazolidine-4-ones Using DSDABCOC as an Effective Media." Combinatorial Chemistry & High Throughput Screening 21, no. 1 (March 20, 2018): 65–69. http://dx.doi.org/10.2174/1386207321666180124094055.
Повний текст джерелаRamachandran, P. Veeraraghavan, and Thomas E. Burghardt. "Recent developments in the chiral synthesis of homoallylic amines via organoboranes." Pure and Applied Chemistry 78, no. 7 (January 1, 2006): 1397–406. http://dx.doi.org/10.1351/pac200678071397.
Повний текст джерелаKumar, Suresh, Bhavna Saroha, Gourav Kumar, Ekta Lathwal, Sanjeev Kumar, Badri Parshad, Meena Kumari, Naveen Kumar, Mabel M. Mphahlele-Makgwane, and Peter R. Makgwane. "Recent Developments in Nanocatalyzed Green Synthetic Protocols of Biologically Potent Diverse O-Heterocycles—A Review." Catalysts 12, no. 6 (June 15, 2022): 657. http://dx.doi.org/10.3390/catal12060657.
Повний текст джерелаGuo, Juan, Huan Guo, Jin Liu, Fangrui Zhong та Yuzhou Wu. "Manganese(II) Oxidizing Bacteria as Whole-Cell Catalyst for β-Keto Ester Oxidation". International Journal of Molecular Sciences 21, № 5 (2 березня 2020): 1709. http://dx.doi.org/10.3390/ijms21051709.
Повний текст джерелаMumtaz, Saira, Mark J. Robertson, and Michael Oelgemöller. "Recent Advances in Photodecarboxylations Involving Phthalimides." Australian Journal of Chemistry 71, no. 9 (2018): 634. http://dx.doi.org/10.1071/ch18220.
Повний текст джерелаFranzén, Robert, and Youjun Xu. "Review on green chemistry Suzuki cross coupling in aqueous media." Canadian Journal of Chemistry 83, no. 3 (March 1, 2005): 266–72. http://dx.doi.org/10.1139/v05-048.
Повний текст джерелаHeywood, Brigid R. "Crystal tectonics: Novel routes to the ordered aggregation and self assembly of inorganic solids." Proceedings, annual meeting, Electron Microscopy Society of America 52 (1994): 424–25. http://dx.doi.org/10.1017/s0424820100169857.
Повний текст джерелаRyckmans, Thomas, Martin P. Edwards, Val A. Horne, Ana Monica Correia, Dafydd R. Owen, Lisa R. Thompson, Isabelle Tran, Michelle F. Tutt, and Tim Young. "Rapid assessment of a novel series of selective CB2 agonists using parallel synthesis protocols: A Lipophilic Efficiency (LipE) analysis." Bioorganic & Medicinal Chemistry Letters 19, no. 15 (August 2009): 4406–9. http://dx.doi.org/10.1016/j.bmcl.2009.05.062.
Повний текст джерелаZiarani, Ghodsi M., Fatemeh Mohajer, Razieh Moradi, and Parisa Mofatehnia. "The Molecular Diversity Scope of Urazole in the Synthesis of Organic Compounds." Current Organic Synthesis 16, no. 7 (December 26, 2019): 953–67. http://dx.doi.org/10.2174/1570179416666190925162215.
Повний текст джерелаBoodida, Sathyanarayana, Parandhama Gudla, and Srinivasula Reddy Maddula. "An Efficient, Novel Synthetic Route to (R)-Salmeterol Xinafoate and Facile Synthetic Protocols for Preparation of its Process Related Potential Impurities." Asian Journal of Chemistry 34, no. 12 (2022): 3333–52. http://dx.doi.org/10.14233/ajchem.2022.26887.
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