Academic literature on the topic 'Halogen exchange reactions'

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Journal articles on the topic "Halogen exchange reactions"

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Bonniface, David W., John D. Scott, Michael J. Watson, et al. "Halogen exchange reactions for CFC alternatives." Green Chemistry 1, no. 1 (1999): 9–11. http://dx.doi.org/10.1039/a808021f.

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Nakada, Masahiro, Sei-ichi Tokumoto, and Minoru Hirota. "Fe3O4-Catalyzed Halogen-Exchange Reactions of Polyhalomethanes." Bulletin of the Chemical Society of Japan 60, no. 11 (1987): 3979–83. http://dx.doi.org/10.1246/bcsj.60.3979.

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Fu, Weimin, Xingya Li, and Xikui Jiang. "Base initiated halogen-exchange reactions between perhaloalkanes." Science in China Series B: Chemistry 40, no. 5 (1997): 475–84. http://dx.doi.org/10.1007/bf02875415.

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Okamoto, Masaki, Hiroyuki Tsukada, Syun Fukasawa, and Aya Sakajiri. "Synthesis of hollow and rattle-type mesoporous silica spheres by treating layered mesoporous silica with a basic solution, and using the spheres as microreactors for two-phase reactions." Journal of Materials Chemistry A 3, no. 22 (2015): 11880–90. http://dx.doi.org/10.1039/c5ta01863c.

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Iddon, Brian, and Brian Iddon. "Metallation and Metal-halogen Exchange Reactions of Imidazoles." HETEROCYCLES 23, no. 2 (1985): 417. http://dx.doi.org/10.3987/r-1985-02-0417.

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Sheppard, Tom D. "Metal-catalysed halogen exchange reactions of aryl halides." Organic & Biomolecular Chemistry 7, no. 6 (2009): 1043. http://dx.doi.org/10.1039/b818155a.

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Bonnafoux, Laurence, Nathalie Nicod, Frederic Leroux, Berengere Quissac, and Francoise Colobert. "New Vistas in Halogen/Metal Exchange Reactions: The Discrimination Between Seemingly Equal Halogens." Letters in Organic Chemistry 3, no. 2 (2006): 165–69. http://dx.doi.org/10.2174/157017806775224279.

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Abe, Hajime, and Hitomi Suzuki. "Copper-Mediated Nucleophilic Displacement Reactions of 1-Haloalkynes. Halogen-Halogen Exchange and Sulfonylation." Bulletin of the Chemical Society of Japan 72, no. 4 (1999): 787–98. http://dx.doi.org/10.1246/bcsj.72.787.

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Geherty, Maryll, James Melnyk, Keith Chomsky та David A. Hunt. "Halogen–metal exchange reactions of bromoaryl-substituted β-lactams". Tetrahedron Letters 54, № 36 (2013): 4934–36. http://dx.doi.org/10.1016/j.tetlet.2013.07.007.

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Gast, Rainer, Thomas Kaukorat, Ion Neda, and Reinhard Schmutzler. "Das 2-Halogen-5,6-benzo-1,3,2-dioxaphosphorinan-4-on-Ringsystem / The 2-Halogeno-5,6-benzo-1,3,2-dioxaphosphorinan-4-one Ring System." Zeitschrift für Naturforschung B 48, no. 7 (1993): 867–74. http://dx.doi.org/10.1515/znb-1993-0703.

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The reaction of salicylic acid with phosphorus trichloride furnished the previously known 2-chloro-5,6-benzo-1,3,2-dioxaphosphorinan-4-one heterocycle 1 which was unambiguously characterized, for the first time, by NMR spectroscopy and mass spectrometry. The fluorine and bromine analogues of 1, 2 and 3 were synthesized from 1, using exchange reactions. The iodo derivative, 4, owing to its instability, could be identified only in the reaction mixture by 1H and 31P NMR spectroscopy. The amine derivatives 5-8 were obtained from 1 using standard exchange reactions, either with silylated amines or
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Dissertations / Theses on the topic "Halogen exchange reactions"

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Khan, N. "Halogen-metal exchange reactions of polybromoimidazoles : Synthesis of thienoimidazoles." Thesis, University of Salford, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.356172.

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Jones, Sally Anne. "Alkali and alkaline earth metal fluoride mediated aromoatic halogen exchange reactions." Thesis, University of Liverpool, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.367085.

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Uenveren, Ercan. "Characterization of Cr 2 O 3 catalysts for Cl/F exchange reactions." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2004. http://dx.doi.org/10.18452/15094.

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Der Cr2O3 ist einer der wichtigsten Katalysatoren im Chlor/Fluor (Cl/F) Austauschreaktionen für die Produktion von chlorofluorocarbon (CFC) Alternativen. Es wird als ein ausgezeichneter heterogener Katalysator für Fluorierung Reaktionen gegründet. Die Dismutierung von CCl2F2 wurde verwendet, um die Wirkung von Halogenierung von Chrom(III) Oxyd auf Cl/F-Austauschreaktionen zu untersuchen und um den Unterschied zwischen den inaktiven und aktiven Katalysatoren herauszufinden. Die heterogenen Reaktionen wurden in einem tubular-flow Ni Reaktor und auch unter simulierten Reaktionsbedingungen in ein
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Machover, Sarah B. "Understanding the Solvent-free Nucleophilic Substitution Reaction Performed in the High Speed Ball Mill (HSBM): Reactions of Secondary Alkyl Halides and Alkali Metal-Halogen Salts." University of Cincinnati / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1307043848.

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Langgaard, Kristensen Jesper. "Metalation, halogen-metal exchange and Pd(0) catalyzed cross-coupling reactions : application to the synthesis of substituted aromatic and heteroaromatic systems /." [Cph.] : Department of Medicinal Chemistry, Royal Danish School of Pharmacy, 2001. http://www.dfh.dk/phd/defences/previous2002.htm.

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Yang, Xiaoyin. "Synthesis of New Functionalized Organocopper Reagents via a Halogen-Copper Exchange Reaction." Diss., lmu, 2005. http://nbn-resolving.de/urn:nbn:de:bvb:19-46863.

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Tiwari, Rohit. "COMPUTATIONAL AND SYNTHETIC STUDIES ON ANTIMETABOLITES FOR ANTICANCER-, ANTIVIRAL-,AND ANTIBIOTIC DRUG DISCOVERY." The Ohio State University, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=osu1267819591.

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Bonnet, Béatrice. "Synthèse et réactivité des èneacétals mono et dihalogénés. Etude de la compétition entre la réaction d'échange halogène-métal et la réaction de métallation." Rouen, 1994. http://www.theses.fr/1994ROUES024.

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Le but de cette thèse est la synthèse des acétals mono et dihalogénés suivie de l'étude de leur réactivité. Elle comprend une étude des différents facteurs influençant la compétition entre les réactions d'échange halogène-métal et de métallation observée à partir de ces composés par action du tertiobutyllithium. La stabilité des carbénoïdes et leur réactivité dépendent de la nature de l'halogène et sont influencées par la présence de sels de lithium. Cette étude a conduit à deux nouveaux réactifs de prénylation. La condensation des lithioacétals obtenus par échange halogène métal à partir de l
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Mongin, Florence. "Régiosélectivité des réactions de bromation, d'échange halogène-métal et de couplage croisé sur des dérivés de la 8-hydroxyquinoléine. Application à la synthèse de pyridocarbazoles." Rouen, 1994. http://www.theses.fr/1994ROUES063.

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Les 8-hydroxy et 8-méthoxyquinoléines étudiées peuvent subir une réaction de bromation ; ainsi sont obtenues des quinoléines diversement substituées par des atomes de brome en position 3, 5 et 7. A partir des 5,7-dibromoquinoléines substituées en position 8, un échange brome-lithium sélectif a été réalisé ; la nature du substituant en position 8 modifie l'orientation de cette réaction. La réaction de couplage croisé, appliquée à diverses bromo-8-méthoxyquinoléines, permet de greffer différents groupements. Dans le cas de dibromoquinoléines, une bonne régiosélectivité a été observée. Enfin, de
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Yang, Xiaoyin [Verfasser]. "Synthesis of new functionalized organocopper reagents via a halogen-copper exchange reaction / von Xiaoyin Yang." 2005. http://d-nb.info/978062752/34.

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Books on the topic "Halogen exchange reactions"

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Khan, Nazir. Halogen-metal exchange reactions of polybromoimidazoles; synthesis of thienoimidazoles. University of Salford, 1985.

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2

Rosyk, Peter John. Some halogen-metal exchange reactions of polybromothiophens: Synthesis of thienothiophens. University of Salford, 1986.

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3

Kreutz, Martin. Halogen-Metall-Austausch bei Bromnaphthalinen: Synthese, Struktur, und Reaktionsweisen mono- und polylithiierter Naphthaline. A.S. Intemann, 1991.

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Book chapters on the topic "Halogen exchange reactions"

1

Edwards, D. A. "By Halogen Exchange." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145180.ch56.

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Mews, R. "From Metathetical Reactions (Halogen-Halogen Exchange)." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145173.ch106.

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Koten, G. Van. "By Metal-Halogen Exchange." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145258.ch73.

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Lee, W. D. "By Homogeneous and Heterogeneous Halogen Exchange." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145173.ch291.

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Wardell, J. L. "By Halogen-Lithium Exchange with Organic Halides1-2." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145258.ch9.

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Noorbatcha, I., B. Arifin, and S. M. Zain. "Ab Initio Quantum Chemical Studies of Six-Center Bond Exchange Reactions Among Halogen and Halogen Halide Molecules." In Computational Science – ICCS 2007. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-72586-2_48.

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7

Prakash, G. K. S., and J. Hu. "Halogen-Exchange Reactions." In Three Carbon-Heteroatom Bonds: Amides and Derivatives; Peptides; Lactams. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-022-00753.

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von Angerer, S. "Halogen-Exchange Reactions." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-00858.

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von Angerer, S. "Halogen-Exchange Reactions." In Science of Synthesis Knowledge Updates KU 2011/1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-116-00367.

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Sai Krishna Murthy, A., R. Tardivel, and R. Grée. "Halogen-Exchange Reactions." In Fluorine. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-034-00211.

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