Статті в журналах з теми "Covalent approaches"
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Tang, Bohan, Jiantao Zhao, Jiang-Fei Xu, and Xi Zhang. "Tuning the stability of organic radicals: from covalent approaches to non-covalent approaches." Chemical Science 11, no. 5 (2020): 1192–204. http://dx.doi.org/10.1039/c9sc06143f.
Повний текст джерелаvan Maarseveen, Jan H., Milo D. Cornelissen, and Simone Pilon. "Covalently Templated Syntheses of Mechanically Interlocked Molecules." Synthesis 53, no. 24 (October 8, 2021): 4527–48. http://dx.doi.org/10.1055/a-1665-4650.
Повний текст джерелаGeorgakilas, Vasilios, Michal Otyepka, Athanasios B. Bourlinos, Vimlesh Chandra, Namdong Kim, K. Christian Kemp, Pavel Hobza, Radek Zboril, and Kwang S. Kim. "Functionalization of Graphene: Covalent and Non-Covalent Approaches, Derivatives and Applications." Chemical Reviews 112, no. 11 (September 25, 2012): 6156–214. http://dx.doi.org/10.1021/cr3000412.
Повний текст джерелаBjij, Imane, Pritika Ramharack, Shama Khan, Driss Cherqaoui, and Mahmoud E. S. Soliman. "Tracing Potential Covalent Inhibitors of an E3 Ubiquitin Ligase through Target-Focused Modelling." Molecules 24, no. 17 (August 28, 2019): 3125. http://dx.doi.org/10.3390/molecules24173125.
Повний текст джерелаSotriffer, Christoph. "Docking of Covalent Ligands: Challenges and Approaches." Molecular Informatics 37, no. 9-10 (June 21, 2018): 1800062. http://dx.doi.org/10.1002/minf.201800062.
Повний текст джерелаKizior, Beata, Mariusz Michalczyk, Jarosław J. Panek, Wiktor Zierkiewicz, and Aneta Jezierska. "Unraveling the Nature of Hydrogen Bonds of “Proton Sponges” Based on Car-Parrinello and Metadynamics Approaches." International Journal of Molecular Sciences 24, no. 2 (January 12, 2023): 1542. http://dx.doi.org/10.3390/ijms24021542.
Повний текст джерелаSainz-Urruela, Carlos, Soledad Vera-López, María Paz San Andrés, and Ana M. Díez-Pascual. "Surface functionalization of graphene oxide with tannic acid: Covalent vs non-covalent approaches." Journal of Molecular Liquids 357 (July 2022): 119104. http://dx.doi.org/10.1016/j.molliq.2022.119104.
Повний текст джерелаSakamaki, Daisuke, Samrat Ghosh, and Shu Seki. "Dynamic covalent bonds: approaches from stable radical species." Materials Chemistry Frontiers 3, no. 11 (2019): 2270–82. http://dx.doi.org/10.1039/c9qm00488b.
Повний текст джерелаGautam, Chandkiram, and Selvam Chelliah. "Methods of hexagonal boron nitride exfoliation and its functionalization: covalent and non-covalent approaches." RSC Advances 11, no. 50 (2021): 31284–327. http://dx.doi.org/10.1039/d1ra05727h.
Повний текст джерелаNigel-Etinger, Izana, Atif Mahammed, and Zeev Gross. "Covalent versus non-covalent (biocatalytic) approaches for enantioselective sulfoxidation catalyzed by corrole metal complexes." Catalysis Science & Technology 1, no. 4 (2011): 578. http://dx.doi.org/10.1039/c1cy00046b.
Повний текст джерелаHussein, Omar A., Khairul Habib, R. Saidur, Ali S. Muhsan, Syed Shahabuddin, and Omer A. Alawi. "The influence of covalent and non-covalent functionalization of GNP based nanofluids on its thermophysical, rheological and suspension stability properties." RSC Advances 9, no. 66 (2019): 38576–89. http://dx.doi.org/10.1039/c9ra07811h.
Повний текст джерелаFairhurst, Robin A., Thomas Knoepfel, Catherine Leblanc, Nicole Buschmann, Christoph Gaul, Jutta Blank, Inga Galuba, et al. "Approaches to selective fibroblast growth factor receptor 4 inhibition through targeting the ATP-pocket middle-hinge region." MedChemComm 8, no. 8 (2017): 1604–13. http://dx.doi.org/10.1039/c7md00213k.
Повний текст джерелаAleman, Elvin A., Heidi S. Pedini, and David Rueda. "Covalent-Bond-Based Immobilization Approaches for Single-Molecule Fluorescence." Biophysical Journal 98, no. 3 (January 2010): 185a. http://dx.doi.org/10.1016/j.bpj.2009.12.990.
Повний текст джерелаAlemán, Elvin A., Heidi S. Pedini, and David Rueda. "Covalent-Bond-Based Immobilization Approaches for Single-Molecule Fluorescence." ChemBioChem 10, no. 18 (December 14, 2009): 2862–66. http://dx.doi.org/10.1002/cbic.200900640.
Повний текст джерелаGottfried, Anna, and Elmar Weinhold. "Sequence-specific covalent labelling of DNA." Biochemical Society Transactions 39, no. 2 (March 22, 2011): 623–28. http://dx.doi.org/10.1042/bst0390623.
Повний текст джерелаNunes, Charneira, Morello, Rodrigues, Pereira, and Antunes. "Mass Spectrometry-Based Methodologies for Targeted and Untargeted Identification of Protein Covalent Adducts (Adductomics): Current Status and Challenges." High-Throughput 8, no. 2 (April 23, 2019): 9. http://dx.doi.org/10.3390/ht8020009.
Повний текст джерелаCuesta, Adolfo, and Jack Taunton. "Lysine-Targeted Inhibitors and Chemoproteomic Probes." Annual Review of Biochemistry 88, no. 1 (June 20, 2019): 365–81. http://dx.doi.org/10.1146/annurev-biochem-061516-044805.
Повний текст джерелаJin, Yinghua, Qi Wang, Philip Taynton, and Wei Zhang. "Dynamic Covalent Chemistry Approaches Toward Macrocycles, Molecular Cages, and Polymers." Accounts of Chemical Research 47, no. 5 (April 16, 2014): 1575–86. http://dx.doi.org/10.1021/ar500037v.
Повний текст джерелаLiu, Chuan-Zhi, Meng Yan, Hui Wang, Dan-Wei Zhang, and Zhan-Ting Li. "Making Molecular and Macromolecular Helical Tubes: Covalent and Noncovalent Approaches." ACS Omega 3, no. 5 (May 11, 2018): 5165–76. http://dx.doi.org/10.1021/acsomega.8b00681.
Повний текст джерелаHossam, Monia, Deena S. Lasheen, and Khaled A. M. Abouzid. "Covalent EGFR Inhibitors: Binding Mechanisms, Synthetic Approaches, and Clinical Profiles." Archiv der Pharmazie 349, no. 8 (June 3, 2016): 573–93. http://dx.doi.org/10.1002/ardp.201600063.
Повний текст джерелаWang, Lei, Jinkyu Han, Jessica Hoy, Fang Hu, Haiqing Liu, Molly M. Gentleman, Matthew Y. Sfeir, James A. Misewich, and Stanislaus S. Wong. "Probing differential optical and coverage behavior in nanotube–nanocrystal heterostructures synthesized by covalent versus non-covalent approaches." Dalton Transactions 43, no. 20 (2014): 7480. http://dx.doi.org/10.1039/c3dt53405g.
Повний текст джерелаBjij, Imane, Fisayo A. Olotu, Clement Agoni, Emmanuel Adeniji, Shama Khan, Ahmed El Rashedy, Driss Cherqaoui, and Mahmoud E. S. Soliman. "Covalent Inhibition in Drug Discovery: Filling the Void in Literature." Current Topics in Medicinal Chemistry 18, no. 13 (October 4, 2018): 1135–45. http://dx.doi.org/10.2174/1568026618666180731161438.
Повний текст джерелаZhang, Weiwei, Linjiang Chen, Sheng Dai, Chengxi Zhao, Cheng Ma, Lei Wei, Minghui Zhu, et al. "Reconstructed covalent organic frameworks." Nature 604, no. 7904 (April 6, 2022): 72–79. http://dx.doi.org/10.1038/s41586-022-04443-4.
Повний текст джерелаSalah, Lakhdar Sidi, Nassira Ouslimani, Dalila Bousba, Isabelle Huynen, Yann Danlée, and Hammouche Aksas. "Carbon Nanotubes (CNTs) from Synthesis to Functionalized (CNTs) Using Conventional and New Chemical Approaches." Journal of Nanomaterials 2021 (September 20, 2021): 1–31. http://dx.doi.org/10.1155/2021/4972770.
Повний текст джерелаVilímová, Iveta, Katel Hervé-Aubert, and Igor Chourpa. "Formation of miRNA Nanoprobes—Conjugation Approaches Leading to the Functionalization." Molecules 27, no. 23 (December 2, 2022): 8428. http://dx.doi.org/10.3390/molecules27238428.
Повний текст джерелаKim, Mi-Sun, Lauriane A. Buisson, Dean A. Heathcote, Haipeng Hu, D. Christopher Braddock, Anthony G. M. Barrett, Philip G. Ashton-Rickardt, and James P. Snyder. "Approaches to design non-covalent inhibitors for human granzyme B (hGrB)." Org. Biomol. Chem. 12, no. 44 (September 23, 2014): 8952–65. http://dx.doi.org/10.1039/c4ob01874e.
Повний текст джерелаZhang, Yanmin, Danfeng Zhang, Haozhong Tian, Yu Jiao, Zhihao Shi, Ting Ran, Haichun Liu, et al. "Identification of Covalent Binding Sites Targeting Cysteines Based on Computational Approaches." Molecular Pharmaceutics 13, no. 9 (August 10, 2016): 3106–18. http://dx.doi.org/10.1021/acs.molpharmaceut.6b00302.
Повний текст джерелаEconomopoulos, Solon P., and Nikos Tagmatarchis. "Multichromophores Onto Graphene: Supramolecular Non-Covalent Approaches for Efficient Light Harvesting." Journal of Physical Chemistry C 119, no. 15 (April 6, 2015): 8046–53. http://dx.doi.org/10.1021/acs.jpcc.5b00731.
Повний текст джерелаSetaro, Antonio, Alphonse Fiebor, Mohsen Adeli, and Stephanie Reich. "Novel Covalent Approaches to Control the Doping Level within Carbon Nanotubes." ECS Meeting Abstracts MA2020-01, no. 7 (May 1, 2020): 701. http://dx.doi.org/10.1149/ma2020-017701mtgabs.
Повний текст джерелаPikabea, Aintzane, and Jacqueline Forcada. "Novel approaches for the preparation of magnetic nanogels via covalent bonding." Journal of Polymer Science Part A: Polymer Chemistry 55, no. 21 (August 3, 2017): 3573–86. http://dx.doi.org/10.1002/pola.28740.
Повний текст джерелаMartínez‐Abadía, Marta, and Aurelio Mateo‐Alonso. "Structural Approaches to Control Interlayer Interactions in 2D Covalent Organic Frameworks." Advanced Materials 32, no. 40 (August 30, 2020): 2002366. http://dx.doi.org/10.1002/adma.202002366.
Повний текст джерелаJamshidiha, Mostafa, Thomas Lanyon-Hogg, Charlotte L. Sutherell, Gregory B. Craven, Montse Tersa, Elena De Vita, Delia Brustur, et al. "Identification of the first structurally validated covalent ligands of the small GTPase RAB27A." RSC Medicinal Chemistry 13, no. 2 (2022): 150–55. http://dx.doi.org/10.1039/d1md00225b.
Повний текст джерелаBartkowski, Michał, and Silvia Giordani. "Supramolecular chemistry of carbon nano-onions." Nanoscale 12, no. 17 (2020): 9352–58. http://dx.doi.org/10.1039/d0nr01713b.
Повний текст джерелаHoyas Pérez, Nadia, and James E. M. Lewis. "Synthetic strategies towards mechanically interlocked oligomers and polymers." Organic & Biomolecular Chemistry 18, no. 35 (2020): 6757–80. http://dx.doi.org/10.1039/d0ob01583k.
Повний текст джерелаDzhardimalieva, Gulzhian I., Bal C. Yadav, Sarkyt E. Kudaibergenov, and Igor E. Uflyand. "Basic Approaches to the Design of Intrinsic Self-Healing Polymers for Triboelectric Nanogenerators." Polymers 12, no. 11 (November 4, 2020): 2594. http://dx.doi.org/10.3390/polym12112594.
Повний текст джерелаGorka, Alexander P., Roger R. Nani, and Martin J. Schnermann. "Cyanine polyene reactivity: scope and biomedical applications." Organic & Biomolecular Chemistry 13, no. 28 (2015): 7584–98. http://dx.doi.org/10.1039/c5ob00788g.
Повний текст джерелаNicholls, Robert A., Robbie P. Joosten, Fei Long, Marcin Wojdyr, Andrey Lebedev, Eugene Krissinel, Lucrezia Catapano, Marcus Fischer, Paul Emsley, and Garib N. Murshudov. "Modelling covalent linkages in CCP4." Acta Crystallographica Section D Structural Biology 77, no. 6 (May 19, 2021): 712–26. http://dx.doi.org/10.1107/s2059798321001753.
Повний текст джерелаBrogi, Simone, Roberta Ibba, Sara Rossi, Stefania Butini, Vincenzo Calderone, Sandra Gemma, and Giuseppe Campiani. "Covalent Reversible Inhibitors of Cysteine Proteases Containing the Nitrile Warhead: Recent Advancement in the Field of Viral and Parasitic Diseases." Molecules 27, no. 8 (April 15, 2022): 2561. http://dx.doi.org/10.3390/molecules27082561.
Повний текст джерелаHarris, Christopher M., Sage E. Foley, Eric R. Goedken, Mark Michalak, Sara Murdock, and Noel S. Wilson. "Merits and Pitfalls in the Characterization of Covalent Inhibitors of Bruton’s Tyrosine Kinase." SLAS DISCOVERY: Advancing the Science of Drug Discovery 23, no. 10 (July 10, 2018): 1040–50. http://dx.doi.org/10.1177/2472555218787445.
Повний текст джерелаOstrem, Jonathan M. L., and Kevan M. Shokat. "Targeting KRAS G12C with Covalent Inhibitors." Annual Review of Cancer Biology 6, no. 1 (April 11, 2022): 49–64. http://dx.doi.org/10.1146/annurev-cancerbio-041621-012549.
Повний текст джерелаKumar, Sushil, Gergo Ignacz, and Gyorgy Szekely. "Synthesis of covalent organic frameworks using sustainable solvents and machine learning." Green Chemistry 23, no. 22 (2021): 8932–39. http://dx.doi.org/10.1039/d1gc02796d.
Повний текст джерелаCui, Daling, Dmitrii F. Perepichka, Jennifer M. MacLeod, and Federico Rosei. "Surface-confined single-layer covalent organic frameworks: design, synthesis and application." Chemical Society Reviews 49, no. 7 (2020): 2020–38. http://dx.doi.org/10.1039/c9cs00456d.
Повний текст джерелаWei, Ying, Yongxia Yan, Xiaoyan Li, Linghai Xie, and Wei Huang. "Covalent nanosynthesis of fluorene-based macrocycles and organic nanogrids." Organic & Biomolecular Chemistry 20, no. 1 (2022): 73–97. http://dx.doi.org/10.1039/d1ob01558c.
Повний текст джерелаMarekha, Bogdan A., Oleg N. Kalugin, and Abdenacer Idrissi. "Non-covalent interactions in ionic liquid ion pairs and ion pair dimers: a quantum chemical calculation analysis." Physical Chemistry Chemical Physics 17, no. 26 (2015): 16846–57. http://dx.doi.org/10.1039/c5cp02197a.
Повний текст джерелаPlet, Benoît, Adéline Delcambre, Stéphane Chaignepain, and Jean-Marie Schmitter. "Affinity ranking of peptide–polyphenol non-covalent assemblies by mass spectrometry approaches." Tetrahedron 71, no. 20 (May 2015): 3007–11. http://dx.doi.org/10.1016/j.tet.2015.02.015.
Повний текст джерелаVoice, Angus, Gary Tresadern, Herman van Vlijmen, and Adrian Mulholland. "Limitations of Ligand-Only Approaches for Predicting the Reactivity of Covalent Inhibitors." Journal of Chemical Information and Modeling 59, no. 10 (September 9, 2019): 4220–27. http://dx.doi.org/10.1021/acs.jcim.9b00404.
Повний текст джерелаZhu, Congzhi, Alexander J. Kalin та Lei Fang. "Covalent and Noncovalent Approaches to Rigid Coplanar π-Conjugated Molecules and Macromolecules". Accounts of Chemical Research 52, № 4 (3 квітня 2019): 1089–100. http://dx.doi.org/10.1021/acs.accounts.9b00022.
Повний текст джерелаChen, Xinyi, Keyu Geng, Ruoyang Liu, Ke Tian Tan, Yifan Gong, Zhongping Li, Shanshan Tao, Qiuhong Jiang, and Donglin Jiang. "Covalent Organic Frameworks: Chemical Approaches to Designer Structures and Built‐In Functions." Angewandte Chemie International Edition 59, no. 13 (March 23, 2020): 5050–91. http://dx.doi.org/10.1002/anie.201904291.
Повний текст джерелаMcAulay, Kirsten, Alan Bilsland, and Marta Bon. "Reactivity of Covalent Fragments and Their Role in Fragment Based Drug Discovery." Pharmaceuticals 15, no. 11 (November 8, 2022): 1366. http://dx.doi.org/10.3390/ph15111366.
Повний текст джерелаGonzález-Sálamo, Javier, Gabriel Jiménez-Skrzypek, Cecilia Ortega-Zamora, Miguel Ángel González-Curbelo, and Javier Hernández-Borges. "Covalent Organic Frameworks in Sample Preparation." Molecules 25, no. 14 (July 20, 2020): 3288. http://dx.doi.org/10.3390/molecules25143288.
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