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Artykuły w czasopismach na temat "Ligand design"
Apostolakist, J., i A. Caflisch. "Computational Ligand Design". Combinatorial Chemistry & High Throughput Screening 2, nr 2 (kwiecień 1999): 91–104. http://dx.doi.org/10.2174/1386207302666220203193501.
Pełny tekst źródłaCaflisch, Amedeo, Rudolf Wälchli i Claus Ehrhardt. "Computer-Aided Design of Thrombin Inhibitors". Physiology 13, nr 4 (sierpień 1998): 182–89. http://dx.doi.org/10.1152/physiologyonline.1998.13.4.182.
Pełny tekst źródłaZhang, Bihan, Jishi Chen, Yitao Cao, Osburg Jin Huang Chai i Jianping Xie. "Ligand Design in Ligand‐Protected Gold Nanoclusters". Small 17, nr 27 (28.01.2021): 2004381. http://dx.doi.org/10.1002/smll.202004381.
Pełny tekst źródłaNash, Jessica A., Matthew D. Manning, Alexey V. Gulyuk, Aleksey E. Kuznetsov i Yaroslava G. Yingling. "Gold nanoparticle design for RNA compaction". Biointerphases 17, nr 6 (listopad 2022): 061001. http://dx.doi.org/10.1116/6.0002043.
Pełny tekst źródłaDate, Richard W., Eva Fernandez Iglesias, Kathryn E. Rowe, James M. Elliott i Duncan W. Bruce. "Metallomesogens by ligand design". Dalton Trans., nr 10 (2003): 1914–31. http://dx.doi.org/10.1039/b212610a.
Pełny tekst źródłaFryzuk, Michael D. "Ligand Design Virtual Issue". Inorganic Chemistry 54, nr 20 (19.10.2015): 9671–74. http://dx.doi.org/10.1021/acs.inorgchem.5b02191.
Pełny tekst źródłaIshiguro, Masaji. "Modeling of receptor–ligand complex and ligand design". Japanese Journal of Pesticide Science 43, nr 1 (20.02.2018): 54–59. http://dx.doi.org/10.1584/jpestics.w18-20.
Pełny tekst źródłaHendrati, Diana, Erianti Siska Purnamasari, Syulastri Effendi i Santhy Wyantuti. "Pemantapan Proses Sintesis Ligan Dibutilditiokarbamat (DBDTK) Sebagai Pengekstrak Logam Tanah Jarang Berdasarkan Desain Eksperimen". ALCHEMY Jurnal Penelitian Kimia 14, nr 2 (3.09.2018): 219. http://dx.doi.org/10.20961/alchemy.14.2.15006.219-235.
Pełny tekst źródłaHendrati, Diana, Erianti Siska Purnamasari, Syulastri Effendi i Santhy Wyantuti. "Pemantapan Proses Sintesis Ligan Dibutilditiokarbamat (DBDTK) Sebagai Pengekstrak Logam Tanah Jarang Berdasarkan Desain Eksperimen". ALCHEMY Jurnal Penelitian Kimia 14, nr 1 (15.02.2018): 195. http://dx.doi.org/10.20961/alchemy.14.1.15006.195-203.
Pełny tekst źródłaHendrati, Diana, Erianti Siska Purnamasari, Syulastri Effendi i Santhy Wyantuti. "Pemantapan Proses Sistesis Ligan Dibutilditiokarbamat (DBDTK) sebagai Pengekstrak Logam Tanah Jarang berdasarkan Desain Eksperimen". ALCHEMY Jurnal Penelitian Kimia 14, nr 1 (15.02.2018): 84. http://dx.doi.org/10.20961/alchemy.14.1.15006.84-99.
Pełny tekst źródłaRozprawy doktorskie na temat "Ligand design"
Kontopidis, George A. "Immunophilin ligand design". Thesis, University of Edinburgh, 2000. http://hdl.handle.net/1842/22386.
Pełny tekst źródłaHallman, Kristina. "Asymmetric Catalysis : Ligand Design and Conformational Studies". Doctoral thesis, KTH, Chemistry, 2001. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-3275.
Pełny tekst źródłaThis thesis deals with the design of ligands for efficientasymmetric catalysis and studies of the conformation of theligands in the catalytically active complexes. All ligandsdeveloped contain chiral oxazoline heterocycles.
The conformations of hydroxy- and methoxy-substitutedpyridinooxazolines and bis(oxazolines) during Pd-catalysedallylic alkylations were investigated using crystallography,2D-NMR techniques and DFT calculations. A stabilising OH-Pdinteraction was discovered which might explain the differencein reactivity between the hydroxy- and methoxy-containingligands. The conformational change in the ligands due to thisinteraction may explain the different selectivities observed inthe catalytic reaction.
Polymer-bound pyridinooxazolines and bis(oxazolines) weresynthesised and employed in Pd-catalysed allylic alkylationswith results similar to those of monomeric analogues;enantioselectivities up to 95% were obtained. One polymer-boundligand could be re-used several times after removal of Pd(0).The polymer-bound bis(oxazoline) was also used in Zn-catalysedDiels-Alder reactions, but the heterogenised catalyst gavelower selectivities than a monomeric analogue.
A series of chiral dendron-containing pyridinooxazolines andbis(oxazolines) were synthesised and evaluated in Pd-catalysedallylic alkylations. The dendrons did not seem to have anyinfluence on the selectivity and little influence on the yieldwhen introduced in the pyridinooxazoline ligands. In thebis(oxazoline) series lower generation dendrimers had a postiveon the selectivity, but the selectivity and the activitydecreased with increasing generation.
Crown ether-containing ligands were investigated inpalladium-catalysed alkylations. No evidence of a possibleinteraction between the metal in the crown ether and thenucleophile was discovered.
A new type of catalyst, an oxazoline-containing palladacyclewas found to be very active in oxidations of secondary alcoholsto the corresponding aldehydes or ketones. The reactions wereperformed with air as the re-oxidant. Therefore, this is anenviromentally friendly oxidation method.
Keywords:asymmetric catalysis, chiral ligand,oxazolines, conformational study, allylic substitution,polymer-bound ligands, dendritic ligands, crown ether,oxidations, palladacycle.
Evans, P. L. "Ligand design for homogenous catalysis". Thesis, University of Oxford, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.376909.
Pełny tekst źródłaGreen, Jason. "Ligand design for copper(I) catalysis". Thesis, University of Hull, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318380.
Pełny tekst źródłaFrost, Jamie Michael. "Ligand design strategies for molecular nanomagnets". Thesis, University of Edinburgh, 2015. http://hdl.handle.net/1842/17990.
Pełny tekst źródłaBremberg, Ulf. "Asymmetric catalysis : ligand design and microwave acceleration". Doctoral thesis, KTH, Chemistry, 2000. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-2962.
Pełny tekst źródłaThis thesis deals partly with the design and synthesis ofligands for use in asymmetric catalysis, and partly with theapplication of microwave heating on metal-based asymmetriccatalytic reactions.
Enantiomerically pure pyridyl alcohols and bipyridylalcohols were synthesized from the chiral pool for future usein asymmetric catalysis. Lithiated pyridines were reacted withseveral chiral electrophiles, yielding diastereomeric mixturesthat could be separated without the use of resolutiontechniques.
New pyridino- and quinolinooxazolines were synthesized andtested in palladium-catalyzed asymmetric allylation using1,3-diphenyl-2-propenyl acetate and dimethyl malonate. Theconformational preferences of the ligands in palladiumcomplexes were studied with crystallography, 2D-NMR techniquesand DFT calculations. Conclusions about how the chirality wastransferred from the ligand to the substrate could be drawnfrom the conformational analysis.
The effect of heating Pd- and Mo-catalyzed asymmetricallylic substitution reactions was investigated with oil bathheating and microwave irradiation. With a few exceptions,ligands with high room temperature selectivity were shown toretain their selectivity on heating. Reaction rates, catalyststability and product selectivities of microwave-heatedreactions were compared with those of reactions performed inoil bath.
Palladium-catalyzed asymmetric allylation was studied withseveral ligand types, allylic substrates and nucleophiles. Someof the experimental procedures had to be adapted to microwaveheating conditions.
The procedure for asymmetric allylation catalyzed bybispyridylamide molybdenum complexes was developed into aone-pot microwave-mediated reaction. With microwaves, Mo(CO)6could be used as an easily-handled metal sourceand inert conditions could be omitted. Derivatives of thebispyridylamide ligandswere synthesized and tested withmolybdenum as catalysts to investigate the effects ofsubstituents on the pyridine ring.
Keywords: ligand, asymmetric catalysis, pyridylalcohols, oxazolines, conformational study, Pd-allyl, fastchemistry, microwave chemistry, Mo-allyl, bispyridylamides.
Jabri, Amir. "Mechanism and ligand design in ruthenium catalysis". Thesis, University of Ottawa (Canada), 2005. http://hdl.handle.net/10393/27208.
Pełny tekst źródłaRio, Echevarria Iria M. "Applications of surface ligand design to flotation". Thesis, University of Edinburgh, 2007. http://hdl.handle.net/1842/3457.
Pełny tekst źródłaBoas, F. Edward. "Physics-based design of protein-ligand binding /". May be available electronically:, 2008. http://proquest.umi.com/login?COPT=REJTPTU1MTUmSU5UPTAmVkVSPTI=&clientId=12498.
Pełny tekst źródłaSpeidel, Joshua A. "Computational approaches to structure based ligand design : an illustration for P/CAF bromodomain ligands /". Access full-text from WCMC, 2007. http://proquest.umi.com/pqdweb?did=1453183061&sid=21&Fmt=2&clientId=8424&RQT=309&VName=PQD.
Pełny tekst źródłaKsiążki na temat "Ligand design"
Hans-Joachim, Böhm, i Gubernator Klaus, red. Structure-based ligand design. Weinheim: Wiley-VCH, 1998.
Znajdź pełny tekst źródłaStradiotto, Mark, i Rylan J. Lundgren, red. Ligand Design in Metal Chemistry. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781118839621.
Pełny tekst źródła(Firm), Knovel, red. Engineering biosensors: Kinetics and design applications. San Diego: Academic Press, 2002.
Znajdź pełny tekst źródłaBallante, Flavio, red. Protein-Ligand Interactions and Drug Design. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1209-5.
Pełny tekst źródłaStoddard, Barry L., red. Computational Design of Ligand Binding Proteins. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3569-7.
Pełny tekst źródłaStorr, Tim, red. Ligand Design in Medicinal Inorganic Chemistry. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118697191.
Pełny tekst źródła1959-, Merz Kenneth M., Ringe Dagmar i Reynolds Charles H. 1957-, red. Drug design: Structure and ligand-based approaches. Cambridge: Cambridge University Press, 2010.
Znajdź pełny tekst źródłaDidier, Rognan, red. Ligand design for G protein-coupled receptors. Weinheim: Wiley, 2006.
Znajdź pełny tekst źródłaMerz, Kenneth M. Drug design: Structure- and ligand-based approaches. Cambridge [U.K.]: Cambridge University Press, 2010.
Znajdź pełny tekst źródłaEngineering biosensors: Kinetics and design applications. San Diego, Calif: Academic, 2002.
Znajdź pełny tekst źródłaCzęści książek na temat "Ligand design"
Wan, Qian-Hong. "Ligand Design". W Mixed-Mode Chromatography, 181–221. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-5485-5_5.
Pełny tekst źródłaSöderhjelm, Pär, Samuel Genheden i Ulf Ryde. "Quantum Mechanics in Structure-Based Ligand Design". W Protein-Ligand Interactions, 121–43. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527645947.ch7.
Pełny tekst źródłaGubernator, K., C. Broger, D. Bur, D. M. Doran, P. R. Gerber, K. Müller i T. M. Schaumann. "Structure-Based Ligand Design". W Computer Aided Drug Design in Industrial Research, 61–77. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-662-03141-4_4.
Pełny tekst źródłaLundgren, Rylan J., i Mark Stradiotto. "Key Concepts in Ligand Design". W Ligand Design in Metal Chemistry, 1–14. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781118839621.ch1.
Pełny tekst źródłaOsten, Kimberly M., Dinesh C. Aluthge i Parisa Mehrkhodavandi. "Ligand Design in Enantioselective Ring-opening Polymerization of Lactide". W Ligand Design in Metal Chemistry, 270–307. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781118839621.ch10.
Pełny tekst źródłaCaballero, Ana, M. Mar Díaz-Requejo, Manuel R. Fructos, Juan Urbano i Pedro J. Pérez. "Modern Applications of Trispyrazolylborate Ligands in Coinage Metal Catalysis". W Ligand Design in Metal Chemistry, 308–29. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781118839621.ch11.
Pełny tekst źródłaMills, David P., i Stephen T. Liddle. "Ligand Design in Modern Lanthanide Chemistry". W Ligand Design in Metal Chemistry, 330–63. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781118839621.ch12.
Pełny tekst źródłaRyken, Scott A., Philippa R. Payne i Laurel L. Schafer. "Tight Bite AngleN,O-Chelates. Amidates, Ureates and Beyond". W Ligand Design in Metal Chemistry, 364–405. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781118839621.ch13.
Pełny tekst źródłaQuigley, Brendan L., i Robert H. Grubbs. "Catalyst Structure andCis-TransSelectivity in Ruthenium-based Olefin Metathesis". W Ligand Design in Metal Chemistry, 15–45. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781118839621.ch2.
Pełny tekst źródłaMüller, Marc-André, i Andreas Pfaltz. "Ligands for Iridium-catalyzed Asymmetric Hydrogenation of Challenging Substrates". W Ligand Design in Metal Chemistry, 46–65. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781118839621.ch3.
Pełny tekst źródłaStreszczenia konferencji na temat "Ligand design"
Rakshit, Pratyusha, Amit Konar, Archana Chowdhury, Eunjin Kim i Atulya K. Nagar. "Muti-objective evolutionary approach of ligand design for protein-ligand docking problem". W 2013 IEEE Congress on Evolutionary Computation (CEC). IEEE, 2013. http://dx.doi.org/10.1109/cec.2013.6557576.
Pełny tekst źródłaGao, Yandong, Dana Brantley-Sieders, Devi Majumdar, Jin Chen, Donna Webb i Deyu Li. "A Simple Approach to Probe the Extracellular Signaling Pathways Using Ligand Traps". W ASME 2012 Third International Conference on Micro/Nanoscale Heat and Mass Transfer. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/mnhmt2012-75106.
Pełny tekst źródłaUcan, Halil Ismet, i Aslihan Yilmaz Obali. "Design of azide-substitued polypyridine ligand". W 2017 IEEE 7th International Conference "Nanomaterials: Application & Properties" (NAP). IEEE, 2017. http://dx.doi.org/10.1109/nap.2017.8190216.
Pełny tekst źródłaTodorov, Nikolay P., i Philip M. Dean. "Computational ligand design by free energy minimization". W The third international symposium on biological physics. AIP, 1999. http://dx.doi.org/10.1063/1.59894.
Pełny tekst źródłaMaccallum, Rob, i Geoff Nitschke. "Automated Ligand Design in Simulated Molecular Docking". W The 2022 Conference on Artificial Life. Cambridge, MA: MIT Press, 2022. http://dx.doi.org/10.1162/isal_a_00482.
Pełny tekst źródłaMurray, Christopher W., David E. Clark, A. David Frenkel, Jin Li, Barry Robson, Bohdan Waszkowycz i David R. Westhead. "Ligand: A new automated system for de novo drug design". W The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47765.
Pełny tekst źródłaJomeh, Sina, i Mina Hoorfar. "Numerical Investigation of the Effect of Geometric and Physiochemical Parameters on Biomolecule Capture Efficiency". W ASME 2010 8th International Conference on Nanochannels, Microchannels, and Minichannels collocated with 3rd Joint US-European Fluids Engineering Summer Meeting. ASMEDC, 2010. http://dx.doi.org/10.1115/fedsm-icnmm2010-30531.
Pełny tekst źródła"Deep Belief Networks for Ligand-Based Virtual Screening of Drug Design". W 2016 the 6th International Workshop on Computer Science and Engineering. WCSE, 2016. http://dx.doi.org/10.18178/wcse.2016.06.115.
Pełny tekst źródłaRichards, Christopher, i Geraint Jones. "Virtual Planar Chirality. A New Approach to Catalyst and Ligand Design". W The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01873.
Pełny tekst źródłaFiguerola-Asencio, Laura, Paula Morales, Dow P. Hurst, Pingwei Zhao, Patricia H. Reggio, Mary E. Abood i Nadine Jagerovic. "Ligand-based drug design approaches for the identification of novel GPR55 modulators". W 6th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07487.
Pełny tekst źródłaRaporty organizacyjne na temat "Ligand design"
Szigethy, Geza. Rational Ligand Design for U(VI) and Pu(IV). Office of Scientific and Technical Information (OSTI), sierpień 2009. http://dx.doi.org/10.2172/972716.
Pełny tekst źródłaRafaeli, Ada, i Russell Jurenka. Molecular Characterization of PBAN G-protein Coupled Receptors in Moth Pest Species: Design of Antagonists. United States Department of Agriculture, grudzień 2012. http://dx.doi.org/10.32747/2012.7593390.bard.
Pełny tekst źródłaClark, Aurora Sue, Nathalie Wall i Paul Benny. Rapid Computer Aided Ligand Design and Screening of Precious Metal Extractants from TRUEX Raffinate with Experimental Validation. Office of Scientific and Technical Information (OSTI), listopad 2015. http://dx.doi.org/10.2172/1232661.
Pełny tekst źródłaJha, Ramesh, Sang-Min Shin i Taraka Dale. Rosetta Comparative Modeling and Ligand Docking for a Transcription Factor Library Design to Select Biosensor for an Anthropogenic Molecule. Office of Scientific and Technical Information (OSTI), czerwiec 2022. http://dx.doi.org/10.2172/1871442.
Pełny tekst źródłaAltstein, Miriam, i Ronald J. Nachman. Rational Design of Insect Control Agent Prototypes Based on Pyrokinin/PBAN Neuropeptide Antagonists. United States Department of Agriculture, sierpień 2013. http://dx.doi.org/10.32747/2013.7593398.bard.
Pełny tekst źródłaRafaeli, Ada, Russell Jurenka i Chris Sander. Molecular characterisation of PBAN-receptors: a basis for the development and screening of antagonists against Pheromone biosynthesis in moth pest species. United States Department of Agriculture, styczeń 2008. http://dx.doi.org/10.32747/2008.7695862.bard.
Pełny tekst źródłaMarshall, G. R. De novo design of ligands for metal separation. 1998 annual progress report. Office of Scientific and Technical Information (OSTI), czerwiec 1998. http://dx.doi.org/10.2172/13746.
Pełny tekst źródłaEyal, Yoram, i Sheila McCormick. Molecular Mechanisms of Pollen-Pistil Interactions in Interspecific Crossing Barriers in the Tomato Family. United States Department of Agriculture, maj 2000. http://dx.doi.org/10.32747/2000.7573076.bard.
Pełny tekst źródłaGottesfeld, Joel M. Inhibition of Estrogen Receptor-Dependent Gene Transcription By a Designed Ligant. Fort Belvoir, VA: Defense Technical Information Center, lipiec 1998. http://dx.doi.org/10.21236/ada357673.
Pełny tekst źródłaAltstein, Miriam, i Ronald Nachman. Rationally designed insect neuropeptide agonists and antagonists: application for the characterization of the pyrokinin/Pban mechanisms of action in insects. United States Department of Agriculture, październik 2006. http://dx.doi.org/10.32747/2006.7587235.bard.
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