Literatura académica sobre el tema "Phosphine – Synthesis"
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Artículos de revistas sobre el tema "Phosphine – Synthesis"
Gusarova, Nina K., Svetlana N. Arbuzova y Boris A. Trofimov. "Novel general halogen-free methodology for the synthesis of organophosphorus compounds". Pure and Applied Chemistry 84, n.º 3 (17 de enero de 2012): 439–59. http://dx.doi.org/10.1351/pac-con-11-07-11.
Texto completoGhosh, Sujit, Kinkar Biswas y Basudeb Basu. "Recent Advances in Microwave Promoted C-P Cross-coupling Reactions". Current Microwave Chemistry 7, n.º 2 (6 de agosto de 2020): 112–22. http://dx.doi.org/10.2174/2213335607666200401144724.
Texto completoDas, Mrinal K., Sarbari Roy, H. Noth y A. Pidcock. "Synthesis and Characterization of Some Phosphine-Boranes and Phosphine- and Phosphite-Cyanoboranes". Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 16, n.º 1 (enero de 1986): 67–75. http://dx.doi.org/10.1080/00945718608055911.
Texto completoAlonso, Concepción, Endika Martín-Encinas, Gloria Rubiales y Francisco Palacios. "Reliable Synthesis of Phosphino- and Phosphine Sulfide-1,2,3,4-Tetrahydroquinolines and Phosphine Sulfide Quinolines". European Journal of Organic Chemistry 2017, n.º 20 (26 de mayo de 2017): 2916–24. http://dx.doi.org/10.1002/ejoc.201700258.
Texto completoPereira, Mariette M., Mário J. F. Calvete, Rui M. B. Carrilho y Artur R. Abreu. "Synthesis of binaphthyl based phosphine and phosphite ligands". Chemical Society Reviews 42, n.º 16 (2013): 6990. http://dx.doi.org/10.1039/c3cs60116a.
Texto completoGusarova, N. K., S. N. Arbusova, S. F. Malysheva, M. Ya Khil'ko, A. A. Tatarinova, V. G. Gorokhov y B. A. Trofimov. "Synthesis of primary phosphines from phosphine and arylethylenes". Russian Chemical Bulletin 44, n.º 8 (agosto de 1995): 1535. http://dx.doi.org/10.1007/bf00714449.
Texto completoMunzeiwa, Wisdom A., Bernard Omondi y Vincent O. Nyamori. "Architecture and synthesis of P,N-heterocyclic phosphine ligands". Beilstein Journal of Organic Chemistry 16 (12 de marzo de 2020): 362–83. http://dx.doi.org/10.3762/bjoc.16.35.
Texto completoChahma, M'hamed, Daniel JT Myles y Robin G. Hicks. "Synthesis, characterization, and coordination chemistry of phosphines with ethylenedioxythiophene substituents". Canadian Journal of Chemistry 83, n.º 2 (1 de febrero de 2005): 150–55. http://dx.doi.org/10.1139/v05-004.
Texto completoPedroarena, James R., Bryan P. Nell, Lev N. Zakharov y David R. Tyler. "Synthesis of Unsymmetrical Bis(phosphine) Oxides and Their Phosphines via Secondary Phosphine Oxide Precursors". Journal of Inorganic and Organometallic Polymers and Materials 30, n.º 1 (21 de agosto de 2019): 196–205. http://dx.doi.org/10.1007/s10904-019-01288-9.
Texto completoSchmalz, Hans-Günther, Mehmet Dindaroğlu y Anna Falk. "A Scalable Synthesis of Chiral Modular Phosphine-Phosphite Ligands". Synthesis 45, n.º 04 (18 de enero de 2013): 527–35. http://dx.doi.org/10.1055/s-0032-1316847.
Texto completoTesis sobre el tema "Phosphine – Synthesis"
Prabagar, Jasotha. "Synthesis of bulky phosphine ligands". Thesis, University of Oxford, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.437012.
Texto completoDai, Xuedong 1970. "Synthesis of novel phosphine ligands". Thesis, Massachusetts Institute of Technology, 1995. http://hdl.handle.net/1721.1/36078.
Texto completoTyzack, Charles Richard. "Stereocontrolled synthesis using phosphine oxides". Thesis, University of Cambridge, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.620349.
Texto completoHutton, Gordon Eric. "Stereocontrol with phosphine oxides". Thesis, University of Cambridge, 1994. https://www.repository.cam.ac.uk/handle/1810/273009.
Texto completoArmstrong, S. K. "Homoallylic amine synthesis using phosphine oxides". Thesis, University of Cambridge, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.596156.
Texto completoArmstrong, Susan Katherine. "Phosphine oxides in homoallyic amine synthesis". Thesis, University of Cambridge, 1991. https://www.repository.cam.ac.uk/handle/1810/272612.
Texto completoSwor, Charles D. (Charles David) 1982. "Synthesis, coordination chemistry, and reactivity of functionalized phosphines: Toward water-soluble macrocyclic phosphine complexes". Thesis, University of Oregon, 2011. http://hdl.handle.net/1794/11264.
Texto completoMacrocyclic phosphine compounds have long been sought as ligands for transition metal complexes because of their strong binding properties. Despite considerable effort in this field, no general methods for synthesizing phosphine macrocycles or their complexes have been developed. This dissertation describes attempts to synthesize an iron complex with a water-soluble macrocyclic tetraphosphine ligand for use in separating nitrogen from natural gas. Chapter I reviews previous syntheses of macrocyclic phosphine ligands and their complexes, focusing on ligand synthesis, coordination chemistry, and demetallation of the complexes. Chapter II reports on the synthesis of water-soluble secondary bidentate phosphine ligands, their coordination chemistry with iron(II), and attempts to use these complexes as templates for forming a macrocyclic iron-phosphine complex by reactions with carbon electrophiles. Over the course of treating these iron complexes with various carbon electrophiles, an interesting reaction between bromomaleic anhydride and proton sponge was discovered. Chapter III explores the product, 4-maleicanhydrido-1,8-bis-(dimethylamino)naphthalene (MAPS). Due to its conjugated donor-acceptor network, which is disrupted upon protonation, MAPS acts as a colorimetric version of a proton sponge. The attachment of MAPS to amine-functionalized solid supports, forming solid-supported proton sponge reagents, is also described. Chapter IV discusses the synthesis of an iron(II) complex of the water-soluble phosphine 1,2-bis(di(hydroxymethyl)phosphino)ethane (DHMPE). Although unbound hydroxymethylphosphines commonly react with NH-functional amines via the phosphorus Mannich reaction, this and other complexes of DHMPE do not undergo this reaction. Further investigation with hydroxymethylphosphine-boranes suggests that the currently-accepted mechanism of the phosphorus Mannich reaction is incorrect, and an alternate mechanism is proposed. Chapter V discusses the synthesis and functionalization of copper(I) complexes of water-soluble phosphines. Unlike the complexes described in Chapter I, these complexes readily react with α,ω-dihalides or di(acyl chloride)s, forming complexes whose mass spectra correspond to those with macrocyclic phosphine ligands. Unlike most macrocyclic tetraphosphine complexes, these complexes can be demetallated by treatment with sulfide. Finally, a new synthesis of water-soluble macrocycles, based on lessons learned during the course of these investigations, is proposed. This dissertation includes previously published and unpublished co-authored material.
Committee in charge: Dr. Michael M. Haley, Chairperson; Dr. David R. Tyler, Advisor; Dr. Darren W. Johnson, Member; Dr. Shih-Yuan Liu, Member; Dr. Mark H. Reed, Outside Member
Lin, Qinghong Chemistry Faculty of Science UNSW. "Chiral phosphine synthesis by the application of directed metallation". Awarded by:University of New South Wales. School of Chemistry, 1999. http://handle.unsw.edu.au/1959.4/19347.
Texto completoPhelps, Jennifer. "Synthesis of homoleptic PT(0) acceptor phosphine complexes". Laramie, Wyo. : University of Wyoming, 2008. http://proquest.umi.com/pqdweb?did=1594481221&sid=1&Fmt=2&clientId=18949&RQT=309&VName=PQD.
Texto completoDriver, Mark Peter. "Synthesis and coordination chemistry of multidentate phosphine ligands". Thesis, Cardiff University, 2016. http://orca.cf.ac.uk/97142/.
Texto completoLibros sobre el tema "Phosphine – Synthesis"
Wiktelius, Daniel. Asymmetric synthesis of dipeptidomimetics and phosphine-boranes: Routes involving stereoselective olefination, expoxidation, and lipase-catalysed reactions. Göteborg: Göteborg University, 2007.
Buscar texto completoYaluma, A. K. Novel chiral phosphines for asymmetric synthesis. Manchester: UMIST, 1995.
Buscar texto completoButt, Afshan Hena. Syntheses of analogues of some important phosphate esters. Birmingham: University of Birmingham, 2001.
Buscar texto completoLee, Sam. Synthesis and characterization of fluorescent-labelled oligoglycols by the phosphite-triester method. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1991.
Buscar texto completoCalcium phosphates in oral biology and medicine. Basel: Karger, 1991.
Buscar texto completoToivari, Mervi. Engineering the pentose phosphate pathway of Saccharomyces cerevisiae for production of ethanol and xylitol. [Espoo, Finland]: VTT Technical Research Centre of Finland, 2007.
Buscar texto completoHealy, Christopher. Synthetic studies on the inhibition of L-myo-inositol 1-phosphate synthase. Birmingham: University of Birmingham, 1991.
Buscar texto completoKürkçüogľu, Išin. The effect of staphylococci on the dissolution of synthetic calcium phosphate biomaterials. Birmingham: University of Birmingham, 2001.
Buscar texto completoTan, Chui Heong. Synthetic studies on the inhibition of L-myo-inositol-1-phosphate synthase. Birmingham: University of Birmingham, 1994.
Buscar texto completoLiu, George Zhigang. Studies on itaconyl bis (sodium methyl phosphate) cross-linked hemoglobin and the synthesis of acyl methyl phosphonates. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1993.
Buscar texto completoCapítulos de libros sobre el tema "Phosphine – Synthesis"
Wang, Zhiming y Ohyun Kwon. "Phosphine Organocatalysis as a Platform for Diversity-Oriented Synthesis". En Diversity-Oriented Synthesis, 97–133. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118618110.ch4.
Texto completoJohnson, Heather C., Thomas N. Hooper y Andrew S. Weller. "The Catalytic Dehydrocoupling of Amine–Boranes and Phosphine–Boranes". En Synthesis and Application of Organoboron Compounds, 153–220. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-13054-5_6.
Texto completoDahlenburg, L. "The Functionalization of Hydrocarbons by Transition Metal Phosphine Complexes: Aspects and Prospects". En Organometallics in Organic Synthesis, 37–50. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-73196-9_2.
Texto completoWeymiens, Wannes, J. Chris Slootweg y Koop Lammertsma. "Phosphine Acetylenic Macrocycles and Cages: Synthesis and Reactivity". En Phosphorus Compounds, 21–55. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-90-481-3817-3_2.
Texto completoStech, Marlitt, Nathanaël Rakotoarinoro, Tamara Teichmann, Anne Zemella, Lena Thoring y Stefan Kubick. "Synthesis of Fluorescently Labeled Antibodies Using Non-Canonical Amino Acids in Eukaryotic Cell-Free Systems". En Methods in Molecular Biology, 175–90. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1406-8_9.
Texto completoManoury, Eric y Rinaldo Poli. "Phosphine-Containing Planar Chiral Ferrocenes: Synthesis, Coordination Chemistry and Applications to Asymmetric Catalysis". En Phosphorus Compounds, 121–49. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-90-481-3817-3_5.
Texto completoLoubser, Christa, Simon Lotz y John E. Ellis. "Tricarbonyl Phosphine, Phosphite, and Arsine Derivatives of Cobalt(I)". En Inorganic Syntheses, 174–82. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132609.ch42.
Texto completoMarriott, Robert C., Jerome D. Odom, Curtis T. Sears, V. D. Bianco y S. Doronzo. "Phosphine". En Inorganic Syntheses, 1–4. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132456.ch1.
Texto completoGokhale, Sudarshan D., William L. Jolly, Sherman Thomas y Doyle Britton. "Phosphine". En Inorganic Syntheses, 56–58. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132401.ch17.
Texto completoRapko, Brian M. "Synthesis, Characterization and Actinide Extraction Behavior of Bridge-Modified Carbamoylmethyl Phosphonates and Phosphine Oxides". En Separations of f Elements, 99–123. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-1406-4_8.
Texto completoActas de conferencias sobre el tema "Phosphine – Synthesis"
He, S., H. Zhang, C. Liu, C. Yang y H. Zeng. "Phosphine-free synthesis of iron selenide nanocrytals". En 2015 IEEE International Magnetics Conference (INTERMAG). IEEE, 2015. http://dx.doi.org/10.1109/intmag.2015.7157346.
Texto completoVo-Thanh, Giang y Huong Nguyen Thi Thu. "Synthesis of Chiral Thiourea-Phosphine Organocatalysts derived from L-Proline". En The 19th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2015. http://dx.doi.org/10.3390/ecsoc-19-a058.
Texto completoEffendy, A. H. White, Abarrul Ikram, Agus Purwanto, Sutiarso, Anne Zulfia, Sunit Hendrana y Zeily Nurachman. "Synthesis and X-ray Structural Study on the Complexes of Silver(I) Halide with Tricyclohexylephosphine, Diphenyl-(2,4,6-trimethoxy)phenylphosphine, Phenyl-2,4,6-trimethoxyphenyl phosphine, and Tris(2,4,6-trimethoxy)phenylphosphine". En NEUTRON AND X-RAY SCATTERING 2007: The International Conference. AIP, 2008. http://dx.doi.org/10.1063/1.2906094.
Texto completoSun, Niefeng, Luhong Mao, K. Sankaranarayanan, Xiaolong Zhou, Weilian Guo, Xiawan Wu y Tongnian Sun. "Synthesis of indium phosphide polycrystalline". En 2008 9th International Conference on Solid-State and Integrated-Circuit Technology (ICSICT). IEEE, 2008. http://dx.doi.org/10.1109/icsict.2008.4734636.
Texto completoSoares, Liliana A., Helena D. de Salles y Paulo H. Schneider. "Highly enantioselective arylation of aromatic aldehydes, promoted by chiral phosphinite ligands". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0018-1.
Texto completoEfimov, V. A. y O. G. Chakhmakhcheva. "Phosphono-PNAs: Synthesis, properties and applications". En XIIth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2002. http://dx.doi.org/10.1135/css200205135.
Texto completoReigosa Chamorro, Francisco, Adolfo Fernández-Figueiras, Fátima Lucio, José Manuel Vila, María Teresa Pereira, Pablo Frieiro y Paula Munín. "Reactivity of functionalized thiosemicarbazone complexes towards phosphines". En The 21st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04744.
Texto completoKIM, J. W., Y. H. CHO, H. J. CHOI y M. S. JHON. "SYNTHESIS AND ELECTRORHEOLOGY OF PHOSPHATE CELLULOSE SUSPENSIONS". En Proceedings of the Eighth International Conference. WORLD SCIENTIFIC, 2002. http://dx.doi.org/10.1142/9789812777546_0083.
Texto completoMunín, Paula, Francisco Reigosa, Fatima Lucio, Pablo Romaris, Juan Ortigueira, Jose Vila y Maria Pereira. "Synthesis and study of the stability of phosphane palladacycles". En The 22nd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2018. http://dx.doi.org/10.3390/ecsoc-22-05765.
Texto completoMarra, Roberta K. F., Alice M. R. Bernardino, Marcos C. de Souza, Gilberto A. Romeiro, María J. Iglesias y Fernando López-Ortiz. "Synthesis of new hemilabile ligands based on phosphinic amide and pyrazolo[1,5-c]quanazoline moieties Applications in coordination chemistry". En 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201381913053.
Texto completoInformes sobre el tema "Phosphine – Synthesis"
Boyd, Bruce A. y Robert H. Neilson. Synthesis of (1,3-Disilylpropenyl)Phosphines. Fort Belvoir, VA: Defense Technical Information Center, enero de 1989. http://dx.doi.org/10.21236/ada204375.
Texto completoLi, B. L., P. Mukherjee y R. H. Neilson. Reactions of an Azidoborane with Phosphines: Synthesis of N-Boryliminophosphoranes. Fort Belvoir, VA: Defense Technical Information Center, enero de 1989. http://dx.doi.org/10.21236/ada204049.
Texto completoCzarnik, Anthony W. Synthetic Catalysts that Hydrolyze Phosphate and Carboxylate Esters. Fort Belvoir, VA: Defense Technical Information Center, septiembre de 1992. http://dx.doi.org/10.21236/ada256420.
Texto completoYusufoglu, Yusuf. Synthesis and characterization of carbonated hydroxyapatite and bioinspired polymer-calcium phosphate nanocomposites. Office of Scientific and Technical Information (OSTI), enero de 2009. http://dx.doi.org/10.2172/976271.
Texto completoWells, Richard L., Mark F. Self, Andrew T. McPhail, Steven R. Aubuchon y Richard C. Woudenberg. Synthesis, Characterization, and Thermal Decomposition of [Cl2GAP(SIME3)2]2, A Potential Precursor to Gallium Phosphide. Fort Belvoir, VA: Defense Technical Information Center, abril de 1993. http://dx.doi.org/10.21236/ada264047.
Texto completoSerne, R. J., W. J. Martin, V. L. LeGore, C. W. Lindenmeier, S. B. McLaurine, P. F. C. Martin y R. O. Lokken. Leach tests on grouts made with actual and trace metal-spiked synthetic phosphate/sulfate waste. Office of Scientific and Technical Information (OSTI), octubre de 1989. http://dx.doi.org/10.2172/5391748.
Texto completoPeng, Xiang-Dong. CATALYST ACTIVITY MAINTENANCE FOR THE LIQUID PHASE SYNTHESIS GAS-TO-DIMETHYL ETHER PROCESS PART II: DEVELOPMENT OF ALUMINUM PHOSPHATE AS THE DEHYDRATION CATALYST FOR THE SINGLE-STEP LIQUID PHASE SYNGAS-TO-DME PROCESS. Office of Scientific and Technical Information (OSTI), mayo de 2002. http://dx.doi.org/10.2172/801222.
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