Relevant bibliographies by topics / Phosphine – Synthesis

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Phosphine – Synthesis'

Author: Grafiati
Published: 4 June 2021
Last updated: 10 February 2022

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Journal articles on the topic "Phosphine – Synthesis"

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Gusarova, Nina K., Svetlana N. Arbuzova, and Boris A. Trofimov. "Novel general halogen-free methodology for the synthesis of organophosphorus compounds." Pure and Applied Chemistry 84, no. 3 (January 17, 2012): 439–59. http://dx.doi.org/10.1351/pac-con-11-07-11.

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The use of novel general halogen-free methodology for the synthesis of phosphines, phosphine chalcogenides, and phosphinic acids from elemental phosphorus and alkenes and alkynes in the superbase suspensions is described.
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Ghosh, Sujit, Kinkar Biswas, and Basudeb Basu. "Recent Advances in Microwave Promoted C-P Cross-coupling Reactions." Current Microwave Chemistry 7, no. 2 (August 6, 2020): 112–22. http://dx.doi.org/10.2174/2213335607666200401144724.

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: Organophosphorous compounds are of potential importance in diverse fields. They are often used as intermediates for making functionalized phosphine ligands as well as find vast applications in the areas of industrial, agricultural and biological chemistry. The microwave-assisted synthesis of C-P bonds has become increasingly popular because of its various advantages over conventional heating in the perspectives of green chemistry. : This review article has primarily focused on the synthesis of various organophosphorous molecules via microwave promoted C-P cross-coupling reactions under metal-catalyzed or metal–free conditions over the last two decades. The synthesis of phosphine ligands on 4,4′-bisquinolone structural framework, disubstituted phosphinic acid esters, vinyl phosphines, aryl- and vinylphosphonates, sugar and nucleoside phosphonates, aminobisphosphonates, triphenyl phosphines, water-soluble tertiary phosphine oxides and many other potentially useful organophosphorous compounds have been illustrated critically. The Hirao reaction, Michaelis-Arbuzov reaction and Sandmeyer type of reactions are generally involved in creating C-P bonds. The role of various metal catalysts, solvents, bases, additives and temperature in different literatures are carefully discussed.
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Das, Mrinal K., Sarbari Roy, H. Noth, and A. Pidcock. "Synthesis and Characterization of Some Phosphine-Boranes and Phosphine- and Phosphite-Cyanoboranes." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 16, no. 1 (January 1986): 67–75. http://dx.doi.org/10.1080/00945718608055911.

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Alonso, Concepción, Endika Martín-Encinas, Gloria Rubiales, and Francisco Palacios. "Reliable Synthesis of Phosphino- and Phosphine Sulfide-1,2,3,4-Tetrahydroquinolines and Phosphine Sulfide Quinolines." European Journal of Organic Chemistry 2017, no. 20 (May 26, 2017): 2916–24. http://dx.doi.org/10.1002/ejoc.201700258.

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Pereira, Mariette M., Mário J. F. Calvete, Rui M. B. Carrilho, and Artur R. Abreu. "Synthesis of binaphthyl based phosphine and phosphite ligands." Chemical Society Reviews 42, no. 16 (2013): 6990. http://dx.doi.org/10.1039/c3cs60116a.

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Gusarova, N. K., S. N. Arbusova, S. F. Malysheva, M. Ya Khil'ko, A. A. Tatarinova, V. G. Gorokhov, and B. A. Trofimov. "Synthesis of primary phosphines from phosphine and arylethylenes." Russian Chemical Bulletin 44, no. 8 (August 1995): 1535. http://dx.doi.org/10.1007/bf00714449.

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Munzeiwa, Wisdom A., Bernard Omondi, and Vincent O. Nyamori. "Architecture and synthesis of P,N-heterocyclic phosphine ligands." Beilstein Journal of Organic Chemistry 16 (March 12, 2020): 362–83. http://dx.doi.org/10.3762/bjoc.16.35.

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Diverse P,N-phosphine ligands reported to date have performed exceptionally well as auxiliary ligands in organometallic catalysis. Phosphines bearing 2-pyridyl moieties prominently feature in literature as compared to phosphines with five-membered N-heterocycles. This discussion seeks to paint a broad picture and consolidate different synthetic protocols and techniques for N-heterocyclic phosphine motifs. The introduction provides an account of P,N-phosphine ligands, and their structural and coordination benefits from combining heteroatoms with different basicity in one ligand. The body discusses the synthetic protocols which focus on P–C, P–N-bond formation, substrate and nucleophile types and different N-heterocycle construction strategies. Selected references are given in relation to the applications of the ligands.
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Chahma, M'hamed, Daniel JT Myles, and Robin G. Hicks. "Synthesis, characterization, and coordination chemistry of phosphines with ethylenedioxythiophene substituents." Canadian Journal of Chemistry 83, no. 2 (February 1, 2005): 150–55. http://dx.doi.org/10.1139/v05-004.

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The preparation of several new phosphines bearing one or more 3,4-ethylenedioxythiophene (EDOT) units as substituents linked at the 2-thienyl position is described. The phosphines were prepared by reaction of lithiated EDOT intermediates with appropriate chlorophosphines to afford (3,4-ethylenedioxy-2-thienyl)diphenylphosphine (1), (bis(3,4-ethylenedioxy-2-thienyl)phenylphosphine (2), tris(3,4-ethylenedioxy-2-thienyl)phosphine (3), 2,5-bis(diphenylphosphino)-3,4-ethylenedioxythiophene (4), and 2-diphenylphosphino-5-mesitylthio-3,4-ethylenedioxythiophene (5). Molybdenum carbonyl complexes of compounds 1–3 were prepared by reaction of the phosphine ligands with cis-Mo(CO)4(pip)2. In all cases, spectroscopic evidence is fully consistent with the phosphines acting as monodentate, P-bound ligands. Electrochemical studies on the phosphines as well as their metal complexes indicate that the normal electrochemical redox robustness of the EDOT group is dramatically decreased by the presence of phosphine substituents: all compounds exhibited irreversible oxidation processes and no evidence of electropolymerization was observed for the phosphines bearing two or three EDOT groups. Key words: phosphines, thiophene, 3,4-ethylenedioxythiophene, EDOT, electrochemistry, coordination complexes.
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Pedroarena, James R., Bryan P. Nell, Lev N. Zakharov, and 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, no. 1 (August 21, 2019): 196–205. http://dx.doi.org/10.1007/s10904-019-01288-9.

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Schmalz, Hans-Günther, Mehmet Dindaroğlu, and Anna Falk. "A Scalable Synthesis of Chiral Modular Phosphine-Phosphite Ligands." Synthesis 45, no. 04 (January 18, 2013): 527–35. http://dx.doi.org/10.1055/s-0032-1316847.

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Dissertations / Theses on the topic "Phosphine – Synthesis"

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Prabagar, Jasotha. "Synthesis of bulky phosphine ligands." Thesis, University of Oxford, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.437012.

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Dai, Xuedong 1970. "Synthesis of novel phosphine ligands." Thesis, Massachusetts Institute of Technology, 1995. http://hdl.handle.net/1721.1/36078.

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Tyzack, Charles Richard. "Stereocontrolled synthesis using phosphine oxides." Thesis, University of Cambridge, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.620349.

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Hutton, Gordon Eric. "Stereocontrol with phosphine oxides." Thesis, University of Cambridge, 1994. https://www.repository.cam.ac.uk/handle/1810/273009.

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Armstrong, S. K. "Homoallylic amine synthesis using phosphine oxides." Thesis, University of Cambridge, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.596156.

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This thesis will describe the development of a new route to homoallylic amines 9, in four steps from alcohols 1, or acetals 2, which may themselves have to be synthesised. The synthesis is stereoselective, and generates E-9 and Z-9 quite separately, thereby avoiding the sometimes difficult separation of these isomers. Alkenes 3, readily available from alcohols 1 or acetals 2, undergo regio- and stereo-selective 1,3-dipolar cycloadditions with nitrile oxides 4 or nitrones 6. The resulting heterocycles 5 and 7 are reductively cleaved to give β-hydroxy-δ-aminoalkyldiphenylphosphine oxides 8. These alcohols undergo Horner-Emmons-type elimination of sodium diphenylphosphinite to give homallylic amines 9, stereospecifically. Isoxazolines 5, resulting from nitrile oxide cycloadditions, undergo stereoselective reduction, and give rise to primary amines 9, R3 = H. Isoxazolines 7, resulting from nitrone cycloadditions, give rise to secondary amines 9, R3 = alkyl or aryl. When the alkoxy substituted alkenes 3, R1 = OR are used, protected enol ethers 9, R1 = OR, R3 = Ac are the final products. The vital cycloaddition and reduction steps are both high yielding, although the elimination is often less so.
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Armstrong, Susan Katherine. "Phosphine oxides in homoallyic amine synthesis." Thesis, University of Cambridge, 1991. https://www.repository.cam.ac.uk/handle/1810/272612.

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Swor, 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.

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xx, 290 p. : ill. (some col.)
Macrocyclic 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
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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.

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The ortho metallation of some aromatic ring systems has been investigated in regard to the influence of several types of phosphorus-centred directing groups upon the reactivity, regioselectivity, and utility in later synthetic elaboration. The metallation step allows derivatisation in several useful ways, offering several routes to the synthesis of novel chiral ditertiary phosphines. Thus, an ortho lithiation of N,N,N',N'-tetramethyl-P-phenylphosphonic diamide (10) led to the interesting primary phosphine, 2-(diphenylphosphino)phenylphosphine (14), after elaboration of the phosphonic diamide directing group. This primary phosphine undergoes an unprecedented facile phenyl group exchange process between its two phosphorus atoms, upon di-lithiation of the primary phosphorus centre. The primary phosphorus centre of (14) has been elaborated in several ways to yield new ditertiary phosphines. The alkylation of this centre in the copper(I) chelate complex has been investigated in several directions. In another direction, (14) has been chemically elaborated to give a new hybrid chiral ditertiary phosphine ligand, "SemiPHOS", containing both a chiral phospholane ring and an adjacent diphenylphosphino group. SemiPHOS has been obtained in optically pure forms by a stereoselective synthesis and, independently, by a resolution procedure on its racemate. The molecular design of SemiPHOS was devised such that, when chelated to a metal atom, a subtle steric interaction appears to allow the chirality of the phospholane ring to influence the neighbouring diphenylphosphino group to adopt a complementary chiral conformation. This idea was tested and evaluated by applying SemiPHOS in catalytic asymmetric hydrogenations of (Z)-a-(Nacylamino) acrylate substrates to produce the R-amino acid precursors. Aryl species lithiated ortho to phosphorus-centred directing groups were coupled oxidatively by a convenient in situ method, to yield biaryl species that could then be elaborated to give biaryl ditertiary phosphine ligands. This method was used to make several atropisomeric chiral ditertiary phosphines.
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Phelps, 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.

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Driver, Mark Peter. "Synthesis and coordination chemistry of multidentate phosphine ligands." Thesis, Cardiff University, 2016. http://orca.cf.ac.uk/97142/.

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The work presented herein is concerned with the design, synthesis and characterisation of novel phosphorus containing ligands and the metal complexes thereof. Chapter 1 will provide an introduction to the field and present an overview of recent developments in the literature. Chapter 2 deals with the development of a synthetic route towards triphosphine macrocycles. The synthesis of bis(2-(phosphino)ethyl)phosphines is presented and their coordination chemistry with first row transition metals (Cr, Fe, Ni, Cu) is described. The ability of these complexes to act as templates in the formation of macrocyclic ligands is assessed. Chapter 3 explores the synthesis of novel chiral multidentate phosphine ligands derived from glycidyl phosphine synthons. The reaction of diphenylglycidyl phosphine with P, N and S based nucleophiles results in the rapid construction of chiral heterodonor ligand frameworks. Preliminary studies of the reactivity of these ligands with metal centres will be presented. Chapter 4 investigates the synthesis of chiral-at-aluminium complexes based upon a novel γ-amino-β-hydroxyphosphine oxide ligand. Two discreet aluminium alkyl complexes were identified and the interconversion of these species was studied by spectroscopic and computational means. Chapter 5 concerns the coordination chemistry of bicyclic multidentate ER-NHCs with Pd(0), Pt(0) and Au(I) metal centres. The M(0) complexes display an unexpected proclivity towards the κ1-C coordination mode. This further informs the discussion of the factors controlling the variable coordination chemistry of such ligands in the design of novel catalytic systems.
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Books on the topic "Phosphine – Synthesis"

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Wiktelius, Daniel. Asymmetric synthesis of dipeptidomimetics and phosphine-boranes: Routes involving stereoselective olefination, expoxidation, and lipase-catalysed reactions. Göteborg: Göteborg University, 2007.

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Yaluma, A. K. Novel chiral phosphines for asymmetric synthesis. Manchester: UMIST, 1995.

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Butt, Afshan Hena. Syntheses of analogues of some important phosphate esters. Birmingham: University of Birmingham, 2001.

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Lee, Sam. Synthesis and characterization of fluorescent-labelled oligoglycols by the phosphite-triester method. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1991.

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Calcium phosphates in oral biology and medicine. Basel: Karger, 1991.

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Toivari, Mervi. Engineering the pentose phosphate pathway of Saccharomyces cerevisiae for production of ethanol and xylitol. [Espoo, Finland]: VTT Technical Research Centre of Finland, 2007.

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Healy, Christopher. Synthetic studies on the inhibition of L-myo-inositol 1-phosphate synthase. Birmingham: University of Birmingham, 1991.

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Kürkçüogľu, Išin. The effect of staphylococci on the dissolution of synthetic calcium phosphate biomaterials. Birmingham: University of Birmingham, 2001.

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Tan, Chui Heong. Synthetic studies on the inhibition of L-myo-inositol-1-phosphate synthase. Birmingham: University of Birmingham, 1994.

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Liu, 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.

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Book chapters on the topic "Phosphine – Synthesis"

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Wang, Zhiming, and Ohyun Kwon. "Phosphine Organocatalysis as a Platform for Diversity-Oriented Synthesis." In Diversity-Oriented Synthesis, 97–133. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118618110.ch4.

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Johnson, Heather C., Thomas N. Hooper, and Andrew S. Weller. "The Catalytic Dehydrocoupling of Amine–Boranes and Phosphine–Boranes." In 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.

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Dahlenburg, L. "The Functionalization of Hydrocarbons by Transition Metal Phosphine Complexes: Aspects and Prospects." In Organometallics in Organic Synthesis, 37–50. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-73196-9_2.

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Weymiens, Wannes, J. Chris Slootweg, and Koop Lammertsma. "Phosphine Acetylenic Macrocycles and Cages: Synthesis and Reactivity." In Phosphorus Compounds, 21–55. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-90-481-3817-3_2.

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Stech, Marlitt, Nathanaël Rakotoarinoro, Tamara Teichmann, Anne Zemella, Lena Thoring, and Stefan Kubick. "Synthesis of Fluorescently Labeled Antibodies Using Non-Canonical Amino Acids in Eukaryotic Cell-Free Systems." In Methods in Molecular Biology, 175–90. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1406-8_9.

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AbstractCell-free protein synthesis (CFPS) enables the development of antibody conjugates, such as fluorophore conjugates and antibody-drug conjugates (ADCs), in a rapid and straightforward manner. In the first part, we describe the cell-free synthesis of antibodies containing fluorescent non-canonical amino acids (ncaa) by using pre-charged tRNA. In the second part, we describe the cell-free synthesis of antibodies containing ncaa by using an orthogonal system, followed by the site-specific conjugation of the fluorescent dye DyLight 650-phosphine. The expression of the antibodies containing ncaa was analyzed by SDS-PAGE, followed by autoradiography and the labeling by in-gel fluorescence. Two different fluorescently labeled antibodies could be generated.
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Manoury, Eric, and Rinaldo Poli. "Phosphine-Containing Planar Chiral Ferrocenes: Synthesis, Coordination Chemistry and Applications to Asymmetric Catalysis." In Phosphorus Compounds, 121–49. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-90-481-3817-3_5.

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Loubser, Christa, Simon Lotz, and John E. Ellis. "Tricarbonyl Phosphine, Phosphite, and Arsine Derivatives of Cobalt(I)." In Inorganic Syntheses, 174–82. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132609.ch42.

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Marriott, Robert C., Jerome D. Odom, Curtis T. Sears, V. D. Bianco, and S. Doronzo. "Phosphine." In Inorganic Syntheses, 1–4. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132456.ch1.

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Gokhale, Sudarshan D., William L. Jolly, Sherman Thomas, and Doyle Britton. "Phosphine." In Inorganic Syntheses, 56–58. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132401.ch17.

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Rapko, Brian M. "Synthesis, Characterization and Actinide Extraction Behavior of Bridge-Modified Carbamoylmethyl Phosphonates and Phosphine Oxides." In Separations of f Elements, 99–123. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-1406-4_8.

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Conference papers on the topic "Phosphine – Synthesis"

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He, S., H. Zhang, C. Liu, C. Yang, and H. Zeng. "Phosphine-free synthesis of iron selenide nanocrytals." In 2015 IEEE International Magnetics Conference (INTERMAG). IEEE, 2015. http://dx.doi.org/10.1109/intmag.2015.7157346.

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Vo-Thanh, Giang, and Huong Nguyen Thi Thu. "Synthesis of Chiral Thiourea-Phosphine Organocatalysts derived from L-Proline." In The 19th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2015. http://dx.doi.org/10.3390/ecsoc-19-a058.

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Effendy, A. H. White, Abarrul Ikram, Agus Purwanto, Sutiarso, Anne Zulfia, Sunit Hendrana, and 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." In NEUTRON AND X-RAY SCATTERING 2007: The International Conference. AIP, 2008. http://dx.doi.org/10.1063/1.2906094.

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Sun, Niefeng, Luhong Mao, K. Sankaranarayanan, Xiaolong Zhou, Weilian Guo, Xiawan Wu, and Tongnian Sun. "Synthesis of indium phosphide polycrystalline." In 2008 9th International Conference on Solid-State and Integrated-Circuit Technology (ICSICT). IEEE, 2008. http://dx.doi.org/10.1109/icsict.2008.4734636.

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Soares, Liliana A., Helena D. de Salles, and Paulo H. Schneider. "Highly enantioselective arylation of aromatic aldehydes, promoted by chiral phosphinite ligands." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0018-1.

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Efimov, V. A., and O. G. Chakhmakhcheva. "Phosphono-PNAs: Synthesis, properties and applications." In 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.

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Reigosa Chamorro, Francisco, Adolfo Fernández-Figueiras, Fátima Lucio, José Manuel Vila, María Teresa Pereira, Pablo Frieiro, and Paula Munín. "Reactivity of functionalized thiosemicarbazone complexes towards phosphines." In The 21st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04744.

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KIM, J. W., Y. H. CHO, H. J. CHOI, and M. S. JHON. "SYNTHESIS AND ELECTRORHEOLOGY OF PHOSPHATE CELLULOSE SUSPENSIONS." In Proceedings of the Eighth International Conference. WORLD SCIENTIFIC, 2002. http://dx.doi.org/10.1142/9789812777546_0083.

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Munín, Paula, Francisco Reigosa, Fatima Lucio, Pablo Romaris, Juan Ortigueira, Jose Vila, and Maria Pereira. "Synthesis and study of the stability of phosphane palladacycles." In The 22nd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2018. http://dx.doi.org/10.3390/ecsoc-22-05765.

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Marra, Roberta K. F., Alice M. R. Bernardino, Marcos C. de Souza, Gilberto A. Romeiro, María J. Iglesias, and Fernando López-Ortiz. "Synthesis of new hemilabile ligands based on phosphinic amide and pyrazolo[1,5-c]quanazoline moieties Applications in coordination chemistry." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201381913053.

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Reports on the topic "Phosphine – Synthesis"

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Boyd, Bruce A., and Robert H. Neilson. Synthesis of (1,3-Disilylpropenyl)Phosphines. Fort Belvoir, VA: Defense Technical Information Center, January 1989. http://dx.doi.org/10.21236/ada204375.

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Li, B. L., P. Mukherjee, and R. H. Neilson. Reactions of an Azidoborane with Phosphines: Synthesis of N-Boryliminophosphoranes. Fort Belvoir, VA: Defense Technical Information Center, January 1989. http://dx.doi.org/10.21236/ada204049.

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Czarnik, Anthony W. Synthetic Catalysts that Hydrolyze Phosphate and Carboxylate Esters. Fort Belvoir, VA: Defense Technical Information Center, September 1992. http://dx.doi.org/10.21236/ada256420.

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4

Yusufoglu, Yusuf. Synthesis and characterization of carbonated hydroxyapatite and bioinspired polymer-calcium phosphate nanocomposites. Office of Scientific and Technical Information (OSTI), January 2009. http://dx.doi.org/10.2172/976271.

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Wells, Richard L., Mark F. Self, Andrew T. McPhail, Steven R. Aubuchon, and 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, April 1993. http://dx.doi.org/10.21236/ada264047.

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Serne, R. J., W. J. Martin, V. L. LeGore, C. W. Lindenmeier, S. B. McLaurine, P. F. C. Martin, and 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), October 1989. http://dx.doi.org/10.2172/5391748.

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Peng, 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), May 2002. http://dx.doi.org/10.2172/801222.

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