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Статті в журналах з теми "Metal-mediated"
Arnold, Frances H., and Ji-Hu Zhang. "Metal-mediated protein stabilization." Trends in Biotechnology 12, no. 5 (May 1994): 189–92. http://dx.doi.org/10.1016/0167-7799(94)90081-7.
Повний текст джерелаBoyarskiy, Vadim P., Nadezhda A. Bokach, Konstantin V. Luzyanin, and Vadim Yu Kukushkin. "Metal-Mediated and Metal-Catalyzed Reactions of Isocyanides." Chemical Reviews 115, no. 7 (March 5, 2015): 2698–779. http://dx.doi.org/10.1021/cr500380d.
Повний текст джерелаKukushkin, Vadim Yu, and Armando J. L. Pombeiro. "Metal-mediated and metal-catalyzed hydrolysis of nitriles." Inorganica Chimica Acta 358, no. 1 (January 2005): 1–21. http://dx.doi.org/10.1016/j.ica.2004.04.029.
Повний текст джерелаHwang, Shyh-Lung, Pouyan Shen, Tzen-Fu Yui, and Hao-Tsu Chu. "Metal-sulfur-COH-silicate fluid mediated diamond nucleation in Kokchetav ultrahigh-pressure gneiss." European Journal of Mineralogy 15, no. 3 (June 10, 2003): 503–11. http://dx.doi.org/10.1127/0935-1221/2003/0015-0503.
Повний текст джерелаR. Cook, Gregory. "Transition Metal-Mediated Kinetic Resolution." Current Organic Chemistry 4, no. 8 (August 1, 2000): 869–85. http://dx.doi.org/10.2174/1385272810004080869.
Повний текст джерелаCook, G. R. "Transition Metal-Mediated Kinetic Resolution." Current Organic Chemistry 4, no. 8 (August 1, 2000): 2. http://dx.doi.org/10.2174/1385272003376021.
Повний текст джерелаSabatino, Valerio, V. B. Unnikrishnan, and Gonçalo J. L. Bernardes. "Transition metal mediated bioorthogonal release." Chem Catalysis 2, no. 1 (January 2022): 39–51. http://dx.doi.org/10.1016/j.checat.2021.12.007.
Повний текст джерелаSilver, S., and T. K. Misra. "Plasmid-Mediated Heavy Metal Resistances." Annual Review of Microbiology 42, no. 1 (October 1988): 717–43. http://dx.doi.org/10.1146/annurev.mi.42.100188.003441.
Повний текст джерелаHernández, Laura P., Almudena González-Álvarez, Ana I. Oliva, and Pablo Ballester. "Metal-mediated multiporphyrin functional assemblies." Journal of Porphyrins and Phthalocyanines 13, no. 04n05 (April 2009): 481–93. http://dx.doi.org/10.1142/s1088424609000693.
Повний текст джерелаGarnovskii, D. A., and Vadim Yu Kukushkin. "Metal-mediated reactions of oximes." Russian Chemical Reviews 75, no. 2 (February 28, 2006): 111–24. http://dx.doi.org/10.1070/rc2006v075n02abeh001188.
Повний текст джерелаДисертації з теми "Metal-mediated"
Howgego, David Christopher. "Metal-mediated molecular machines." Thesis, University of Edinburgh, 2013. http://hdl.handle.net/1842/7619.
Повний текст джерелаButters, Christopher. "Metal mediated organic transformations." Thesis, University of Bath, 1995. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.260230.
Повний текст джерелаTrussell, Stephen John. "Transition metal-mediated organosilicon chemistry." Thesis, Imperial College London, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.298136.
Повний текст джерелаLindup, Richard J. "Metal-mediated borylation of fluorocarbons." Thesis, University of York, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.434017.
Повний текст джерелаBaxter, John S. "Transition metal mediated annulation reactions." Thesis, University of Bristol, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.324243.
Повний текст джерелаWarner, Benjamin Peter. "Mechanisms of metal-mediated cyclizations." Thesis, Massachusetts Institute of Technology, 1995. http://hdl.handle.net/1721.1/36008.
Повний текст джерелаEriksson, Ludvig. "Transition Metal Mediated Transformations of Carboranes." Doctoral thesis, Uppsala University, Organic Chemistry, 2003. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3324.
Повний текст джерелаThis thesis describes the use of copper and palladium to mediate transformations of carboranes, especially p-carborane.
1-(1-p-carboranyl)-N-methyl-N-(2-butyl)-3-isoquinolinecarboxamide, a carborane containing analogue of the peripheral benzodiazepine receptor (PBR) ligand PK11195, has been synthesised. A key step in the reaction is the copper (I) mediated coupling of p-carborane with ethyl 1-bromo-isoquinoline-3-carboxylate.
p-Carborane has been arylated on the 2-B-atom in high yields, using the Suzuki–Miyaura reaction. Thus the reaction between 2-I-p-carborane and various arylboronic acids [1-naphthyl-, phenyl-, 4-MeO-C6H4-, 3-CH3CONH-C6H4-, 4-NC-C6H4-, 3-NO2-C6H4-], gave the corresponding 2-aryl-p-carboranes in DME solution when reacted in the presence of cesium fluoride and the catalytic Pd2(dba)3–dppb system. Under the same conditions, the boron-boron bond forming reaction of two p-carboranylboronic esters (2-[(pinacolato)boron]-p-carborane and 2-[(neopentyl glycolato)boron]-p-carborane) was also shown feasible.
p-Carborane has been vinylated on the 2-B-atom in high yields by use of the Heck reaction. The coupling between 2-I-p-carborane and various styrenes [4-H-, 4-C6H4-, 4-Cl , 4-Br-, 4-NO2-, 4-CH3O- and 4 CH3 ] resulted in the formation of the correspondingtrans-β-(2-B-p-carboranyl) styrene in DMF solution when reacted in the presence of silver phosphate and the palladacycle Herrmann´s catalyst. The reaction was shown to proceed at higher rate with electron rich than with electron deficient olefins.
The feasibility of palladium-catalysed isotopic exchange of an iodinated closo-carborane with a radioisotope of iodine has been studied. 2-I-p-carborane was selected as a model compound. It was shown, that such isotopic exchange is possible and provides a high yield (83 ± 4.2 %) during 40 min long reaction. The reaction conditions were optimised, and it was demonstrated that presence of the tetra n-butylammonium hydrogensulphate is important in order to stabilise catalyst and provide reproducibility of labelling. In this work we have modified the methodology and extended the application to a wider range of iodinated carboranes. By the use of Herrmann’s catalyst in toluene at 100 °C this [125I]-iodide labelling could be improved and extended. 2-I-p- 9-I-m-, 9-I-o-, 3-I-o-carborane, 1-phenyl-3-I-o-carborane and 1,2-diphenyl-3-I-o-carborane could be [125I]-iodide labelled in high to excellent yields within 5 minutes.This reported palladium catalyzed radio-iodination of the uncharged closo-carboranes might find use in pharmacokinetic studies of carborane derivatives.
McAlonan, Helena M. "Transition metal mediated approaches to pumiliotoxins." Thesis, Queen's University Belfast, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318792.
Повний текст джерелаShaw, Graham Andrew. "Solvent mediated synthesis of metal chalcogenides." Thesis, University College London (University of London), 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326065.
Повний текст джерелаHunter, Rupert Alexander. "Transition metal mediated synthesis of heterocycles." Thesis, University of Southampton, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.402426.
Повний текст джерелаКниги з теми "Metal-mediated"
Tanaka, Ken, ed. Transition-Metal-Mediated Aromatic Ring Construction. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118629871.
Повний текст джерелаKhosravi, Ezat, Yusuf Yagci, and Yuri Savelyev, eds. New Smart Materials via Metal Mediated Macromolecular Engineering. Dordrecht: Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-90-481-3278-2.
Повний текст джерелаFergani, Hadi Khamis. Metal-atom mediated chemical transformations: The reaction of group 13 metal atoms with arenes. Sudbury, Ont: Laurentian University, Chemistry and Biochemistry Department, 1999.
Знайти повний текст джерелаEvangelos, Manias, Malliaras George G, and Symposium A, "Defect Mediated Phenomena in Ordered Polymers" (2002 : Boston, Mass.), eds. Polymer/metal interfaces and defect mediated phenomena in ordered polymers: Symposia held December 2-6, 2002, Boston, Massachusetts, U.S.A. Warrendale, Pa: Materials Research Society, 2003.
Знайти повний текст джерелаI. Radical Cyclizations Mediated by Transition Metal Hydrides II. Study toward the Total Synthesis of Pluraflavin A III. Cytoprotective Polyacetylenes Inspired by Panaxytriol. [New York, N.Y.?]: [publisher not identified], 2012.
Знайти повний текст джерелаTanaka, Ken. Transition-Metal-Mediated Aromatic Ring Construction. Wiley & Sons, Limited, John, 2013.
Знайти повний текст джерелаTanaka, Ken. Transition-Metal-Mediated Aromatic Ring Construction. Wiley & Sons, Incorporated, John, 2013.
Знайти повний текст джерелаTanaka, Ken. Transition-Metal-Mediated Aromatic Ring Construction. Wiley & Sons, Incorporated, John, 2013.
Знайти повний текст джерелаMetal Mediated Template Synthesis of Ligands. World Scientific Publishing Company, 2004.
Знайти повний текст джерелаTanaka, Ken. Transition-Metal-Mediated Aromatic Ring Construction. Wiley & Sons, Incorporated, John, 2013.
Знайти повний текст джерелаЧастини книг з теми "Metal-mediated"
Ciofi-Baffoni, Simone. "Metal-Mediated Interactions." In NMR of Biomolecules, 196–203. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527644506.ch10.
Повний текст джерелаChen, Chuan-Feng, and Yun Shen. "Metal-Mediated Reactions." In Helicene Chemistry, 87–115. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-53168-6_5.
Повний текст джерелаChalker, Justin M. "Metal-Mediated Bioconjugation." In Chemoselective and Bioorthogonal Ligation Reactions, 231–70. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2017. http://dx.doi.org/10.1002/9783527683451.ch8.
Повний текст джерелаFarrell, Nicholas. "Metal-Mediated Antibiotic Action." In Transition Metal Complexes as Drugs and Chemotherapeutic Agents, 168–82. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-011-7568-5_8.
Повний текст джерелаHong, Jing, Olesya A. Kharenko, Mikhail V. Tsurkan, and Michael Y. Ogawa. "Metal-Mediated Peptide Assembly." In ACS Symposium Series, 167–82. Washington, DC: American Chemical Society, 2009. http://dx.doi.org/10.1021/bk-2009-1012.ch011.
Повний текст джерелаShimizu, Makoto, Iwao Hachiya, and Junji Inanaga. "Metal Iodides-Mediated Reaction." In Iodine Chemistry and Applications, 329–51. Hoboken, NJ: John Wiley & Sons, Inc, 2014. http://dx.doi.org/10.1002/9781118909911.ch18.
Повний текст джерелаPandey, Vidya Dhar. "Cyanobacteria-Mediated Heavy Metal Remediation." In Agro-Environmental Sustainability, 105–21. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-49727-3_6.
Повний текст джерелаHerndon, James Wallace. "Utilization of Transition-Metal Carbenoids." In Transition-Metal-Mediated Aromatic Ring Construction, 425–53. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118629871.ch17.
Повний текст джерелаNishibayashi, Yoshiaki. "Cycloaromatization via Transition Metal-Cumulenylidenes." In Transition-Metal-Mediated Aromatic Ring Construction, 549–69. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118629871.ch21.
Повний текст джерелаGandon, Vincent. "Cobalt-Mediated [2 + 2 + 2] Cycloaddition." In Transition-Metal-Mediated Aromatic Ring Construction, 1–35. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118629871.ch1.
Повний текст джерелаТези доповідей конференцій з теми "Metal-mediated"
Sun, Yugang, and Younan Xia. "Polymer-mediated synthesis of metal nanostructures." In Optical Science and Technology, SPIE's 48th Annual Meeting, edited by Guozhong Cao, Younan Xia, and Paul V. Braun. SPIE, 2003. http://dx.doi.org/10.1117/12.504822.
Повний текст джерелаShahbazyan, Tigran V., and Vitaliy N. Pustovit. "Surface-plasmon-mediated energy transfer near metal nanoparticles." In SPIE NanoScience + Engineering, edited by Mark I. Stockman. SPIE, 2011. http://dx.doi.org/10.1117/12.893232.
Повний текст джерелаSu, Ding, Tian Yanhong, and He Xiaobin. "Polyol synthesis of silver nanowires with metal ions mediated." In 2013 14th International Conference on Electronic Packaging Technology (ICEPT). IEEE, 2013. http://dx.doi.org/10.1109/icept.2013.6756688.
Повний текст джерелаNaik, Gururaj V., Alex A. Welch, and Jennifer A. Dionne. "Hot-carrier mediated photon upconversion in metal/semiconductor heterostructure." In CLEO: QELS_Fundamental Science. Washington, D.C.: OSA, 2016. http://dx.doi.org/10.1364/cleo_qels.2016.fw1b.1.
Повний текст джерелаZhang, Minchang, Trevor Allen, and Ray DeCorby. "Admittance-matched plasmon-mediated tunneling through dielectric-metal-dielectric multilayers." In Optical Interference Coatings. Washington, D.C.: OSA, 2013. http://dx.doi.org/10.1364/oic.2013.ta.8.
Повний текст джерелаYang, Ziming, Yiju Liao, and Alexandria Aspin. "Dissolved metal-mediated organic carbon transformations in oceanic hydrothermal systems." In Goldschmidt2022. France: European Association of Geochemistry, 2022. http://dx.doi.org/10.46427/gold2022.9958.
Повний текст джерелаLe Guevel, Xavier, Benjamin Musnier, Karl D. Wegner, Maxime Henry, Agnes Desroches-Castan, Ute Resch-Genger, Sabine Bailly, Yves Usson, Véronique Josserand, and Jean-Luc Coll. "Surface chemistry-mediated metal nanoclusters for in vivo shortwave infrared imaging." In Colloidal Nanoparticles for Biomedical Applications XVI, edited by Marek Osiński and Antonios G. Kanaras. SPIE, 2021. http://dx.doi.org/10.1117/12.2577451.
Повний текст джерелаCiattoni, Alessandro, Andrea Marini, and Claudio Conti. "Phase-matching-free parametric oscillation mediated by monolayer transition metal dichalcogenides." In Nonlinear Optics. Washington, D.C.: OSA, 2019. http://dx.doi.org/10.1364/nlo.2019.nf1a.2.
Повний текст джерелаOno, Akira, Itaru Okamoto, Hideo Urata, Hidetake Torigoe, Hisao Saneyoshia, Jiro Kondo, and Yoshiyuki Tanaka. "Syntheses and characterizations of DNA duplexes having metal ion mediated base pairs." In XVIth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2014. http://dx.doi.org/10.1135/css201414014.
Повний текст джерелаHayashi, Gosuke, and Akimitsu Okamoto. "Metal-mediated reactions to detect 5-methylcytosine and 5-hydroxymethylcytosine in DNA." In XVIth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2014. http://dx.doi.org/10.1135/css201414088.
Повний текст джерелаЗвіти організацій з теми "Metal-mediated"
Baker, R. T. Tandem metal-mediated synthesis. Office of Scientific and Technical Information (OSTI), December 1998. http://dx.doi.org/10.2172/350837.
Повний текст джерелаSen, Ayusman. Transition metal mediated transformations of small molecules. Office of Scientific and Technical Information (OSTI), March 2017. http://dx.doi.org/10.2172/1346019.
Повний текст джерелаSen, A. [Transition metal mediated transformations of small molecules]. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/6915678.
Повний текст джерелаSen, A. Transition metal mediated transformations of small molecules. Office of Scientific and Technical Information (OSTI), May 1990. http://dx.doi.org/10.2172/6971891.
Повний текст джерелаSen, A. [Transition metal mediated transformations of small molecules]. Progress report. Office of Scientific and Technical Information (OSTI), October 1992. http://dx.doi.org/10.2172/10188286.
Повний текст джерелаNicholas, Kenneth M. Transition metal-mediated thermal and photochemical carbon dioxide conversion. Office of Scientific and Technical Information (OSTI), January 2000. http://dx.doi.org/10.2172/765234.
Повний текст джерелаDentinger, Paul M., and Srikant Pathak. Highly specific electronic signal transduction mediated by DNA/metal self-assembly. Office of Scientific and Technical Information (OSTI), November 2003. http://dx.doi.org/10.2172/918237.
Повний текст джерелаGmeiner, William H. Metal Occupancy of Zinc Finger Motifs as Determinants for Zn2+-Mediated Chemosensitization of Prostate Cancer Cells. Fort Belvoir, VA: Defense Technical Information Center, December 2013. http://dx.doi.org/10.21236/ada596731.
Повний текст джерелаNicholas, Kenneth M. Transition Metal-Mediated Thermal and Photochemical Carbon Dioxide Conversion. Final report, March 15, 1995-March 14, 1998. Office of Scientific and Technical Information (OSTI), November 1995. http://dx.doi.org/10.2172/761340.
Повний текст джерелаNicholas, K. M. Transition metal-mediated thermal and photochemical carbon dioxide activation. Progress report, March 15, 1990--March 14, 1991. Office of Scientific and Technical Information (OSTI), December 1990. http://dx.doi.org/10.2172/10172147.
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