Bibliografías temáticas / Ligands – Synthesis

Literatura académica sobre el tema "Ligands – Synthesis"

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Publicado: 4 de junio de 2021
Última modificación: 13 de febrero de 2022

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Artículos de revistas sobre el tema "Ligands – Synthesis"

1

U C Mashelkar, U. C. Mashelkar y V. Pandey V Pandey. "Synthesis of Some Novel Ligands of Benzimidazole Derivatives". Indian Journal of Applied Research 4, n.º 8 (1 de octubre de 2011): 596–97. http://dx.doi.org/10.15373/2249555x/august2014/157.

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Srivastava, Abhishek, Neetu Srivastava, Umesh NathTripathi y Afshan Siddiqui. "Synthesis and Characterization of Mixed Ligand Complexes of Zirconium(IV) with Sulphur, Nitrogen and Oxygen Donor Ligands". Chemistry & Chemical Technology 13, n.º 1 (5 de marzo de 2019): 23–32. http://dx.doi.org/10.23939/chcht13.01.023.

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Semeniuchenko, Volodymyr, Volodymyr Khilya y Ulrich Groth. "Highly Efficient Synthesis of (Phosphinodihydrooxazole)- (1,5-cyclooctadiene) Iridium Complexes". Zeitschrift für Naturforschung B 64, n.º 10 (1 de octubre de 2009): 1147–58. http://dx.doi.org/10.1515/znb-2009-1007.

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A highly efficient one-pot procedure for the synthesis of complexes of the type [Ir(COD)(Phox)]X, where Phox is a (chiral) phosphinooxazoline ligand, X = PF6 or B[(3,5-(CF3)2C6H3)]4 (BARF), is developed. Former reported syntheses demanded the isolation of pure ligands by column chromatography, but the ligands tend to adsorb irreversibly on silica. Moreover, the chromatography has to be performed with careful exclusion of air. The present method avoids this difficulties. The yields of the syntheses are comparable with those starting from the pure ligands. The method is also suitable for the preparation of complexes of the type [Rh(COD)(Phox)]BARF and [Rh(Phox)2]BARF.
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Huang, Jianhui, Caifeng Li, Liu Liu y Xuegang Fu. "Norbornene in Organic Synthesis". Synthesis 50, n.º 15 (25 de junio de 2018): 2799–823. http://dx.doi.org/10.1055/s-0037-1610143.

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The norbornene skeleton possesses an alkene functionality with a fixed conformation, and represents unique reactivity. The use of norbornene and analogues as substrates is overviewed; reactivities are discussed as well as the role of norbornenes as ligands assisting modern organic transformations.1 Introduction2 Synthesis of Substituted Norbornenes2.1 Preparation of Functionalized Norbornenes by Deprotonation and Substitution Reactions2.2 Preparation of Functionalized Norbornenes under Palladium-Catalyzed­ Reaction Conditions2.3 Alkylation of Norbornene2.4 Multistep Synthesis3 Synthesis of Substituted Norbornanes3.1 Three-Membered-Ring Formation3.2 Formation of Four-Membered Rings3.3 Five- and Six-Membered Ring Formation3.4 Syntheses of Difunctionalized Norbornanes4 Synthesis of Cyclopentanes4.1 Oxidation Reactions4.2 Ring-Opening Cross Metathesis (ROCM)4.3 Ring-Opening Metathesis Polymerization (ROMP)4.4 Palladium-Catalyzed Ring-Opening of Norbornene5 Norbornene-Mediated Reactions5.1 Palladium Insertion into Carbon–Halide Bonds5.2 Palladium Insertion into N–H and C–H Bonds5.3 Norbornene as Ligand in Mediated Reactions6 Conclusion
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Heutz, Frank J. L., Michiel C. Samuels y Paul C. J. Kamer. "Solid-phase synthesis of recyclable diphosphine ligands". Catalysis Science & Technology 5, n.º 6 (2015): 3296–301. http://dx.doi.org/10.1039/c5cy00287g.

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The first efficient solid-phase synthetic approach towards diphosphine ligands is demonstrated. This modular method offers facile access to a class of ligands providing huge potential for ligand fine-tuning.
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6

Knibbs, R. N., R. A. Craig, S. Natsuka, A. Chang, M. Cameron, J. B. Lowe y L. M. Stoolman. "The fucosyltransferase FucT-VII regulates E-selectin ligand synthesis in human T cells." Journal of Cell Biology 133, n.º 4 (15 de mayo de 1996): 911–20. http://dx.doi.org/10.1083/jcb.133.4.911.

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Selectin-ligands on T cells contribute to the recruitment of circulating cells into chronic inflammatory lesions in the skin and elsewhere. This report provides the first evidence that a single fucosyltransferase, termed FucT-VII, controls the synthesis of E-selectin ligands in human T-lymphoblasts. The FucT-IV transferase (the ELFT enzyme), in contrast constructs lower avidity E-selectin ligands and requires enzyme levels found only in myeloid cells. Treatment of Jurkat cells with phorbol myristate acetate increased the expression of sialylated Lewis(x)-related sLe(x)related epitopes and induced the synthesis of E-selectin ligands functional at physiologic levels of linear shear-stress. Northern analysis revealed a parallel increase in the steady-state levels FucT-VII mRNA, but there were no increases in the two other leukocyte-associated fucosyltransferases (FucT-IV and VI). The stable transfection of the FucT-VII gene into Jurkat cells induced high levels of the sLe(x)-related epitopes and the synthesis of E-selectin ligands which equal or exceeded the avidity of those on circulating lymphocytes. The growth of T-lymphoblasts under conditions which induced expression of the sLe(x,a) epitopes increased the level of FucT-VII mRNA, the synthesis of sialylated-Lewis(x) structures by cell-free extracts and the synthesis of E-selectin ligands equal in avidity to those on FucT-VII transfectants. In contrast, neither the mRNA levels nor activities of the FucT-IV and VI enzymes increased in association with E-selectin ligand synthesis in T-lymphoblasts. Myeloid cell lines, unlike lymphoblasts, expressed high levels of both the FucT-VII and IV enzymes in conjunction with E-selectin ligands raising the possibility that both enzymes contributed to ligand synthesis. FucT-IV transfected Jurkat cells synthesized low avidity ligands for E-selectin but only in association with CDw65 (VIM-2) carbohydrate epitope. Only blood neutrophils and myeloid cell lines expressed this epitope at the levels associated with E-ligand synthesis in the transfectants. In contrast, native Jurkat cells, blood monocytes, blood lymphocytes, and cultured T-lymphoblasts expressed low levels or none. We conclude that FucT-VII is a principal regulator of E-selectin ligand synthesis in human T-lymphoblasts while both FucT-VII and FucT-IV may direct ligand synthesis in some myeloid cells.
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Bednářová, Eva, Štefan Malatinec y Martin Kotora. "Applications of Bolm’s Ligand in Enantioselective Synthesis". Molecules 25, n.º 4 (20 de febrero de 2020): 958. http://dx.doi.org/10.3390/molecules25040958.

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One pathway for the preparation of enantiomerically pure compounds from prochiral substrates is the use of metal complex catalysis with chiral ligands. Compared to the other frequently used chiral ligands, chiral 2,2’-bipyridines have been underexploited, despite the data indicating that such ligands have considerable potential in synthetic chemistry. One of those is the so-called Bolm’s ligand, a compound possessing chiral alcohol moieties in the side chains attached to the 2,2’-bipyridine scaffold. Various metal salts have been used in combination with Bolm’s ligand as potent catalysts able to bring about enantioselective alkylations, allylations, conjugate additions, desymmetrization of meso-epoxides, aldol reactions, etc. This review aims to summarize Bolm’s ligand applications in the area of enantioselective synthesis over the last three decades since its preparation.
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Ranskiy, Anatoliy y Natalia Didenko. "Direct Synthesis of Cuprum(II) Complex Compounds Based on Thioamide Ligands". Chemistry & Chemical Technology 8, n.º 4 (5 de diciembre de 2014): 371–78. http://dx.doi.org/10.23939/chcht08.04.371.

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Ghesner, Ioan, Warren E. Piers, Masood Parvez y Robert McDonald. "Synthesis and coordination chemistry of 2,2′-diboratabiphenyls". Canadian Journal of Chemistry 84, n.º 2 (1 de febrero de 2006): 81–92. http://dx.doi.org/10.1139/v05-220.

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Dianionic 2,2′-diboratabiphenyl derivatives were prepared as a new class of binucleating ligands. Preliminary investigations into their coordination chemistry involved Rh complexes. Their solution and solid state structures were studied and confirm the preference for η6–η6 coordination of the novel ligands, rendering them isoelectronic analogues of the ubiquitous bicyclopentadienyl system. Comparative studies suggest stronger donor properties for the fulvalene ligand as compared with the 2,2′-diboratabiphenyl system.Key words: dinucleating ligands, bimetallic complexes, rhodium complexes, boron heterocycles, X-ray structure.
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10

Caputo, Christine A., Florentino d. S. Carneiro, Michael C. Jennings y Nathan D. Jones. "Modular syntheses of oxazolinylamine ligands and characterization of group 10 metal complexes". Canadian Journal of Chemistry 85, n.º 2 (1 de febrero de 2007): 85–95. http://dx.doi.org/10.1139/v06-188.

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The syntheses of aminoalkyloxazoline and pyrrolidinyloxazoline ligands, each of which bear a pair of chiral centres, by both known and new routes are reported. Variable temperature NMR studies show that the known stepwise syntheses of the pyrrolidinyl compounds are not complicated by epimerization; however, coordination of one of the aminoalkyl derivatives to Pt(II) under conditions of prolonged heating to 80 °C does give mixtures of diastereomeric N,N ′-chelated complexes that result from inversion of the chiral centre associated with the aminoalkyl fragment. A new synthesis of pyrrolidinyloxazoline ligands that involves the Zn-catalyzed cyclization of Cbz-protected 2-cyanopyrrolidine and β-amino alcohols is also reported. This procedure offers the advantages of economy, shorter time, and fewer purification steps over the previously reported synthesis. In addition, the crystal structure of an enantiopure Pd(II) complex of an N,N ′-chelated pyrrolidinyloxazoline is disclosed. This compound has a pseudo-C2 axis of symmetry, which may make it suitable for asymmetric catalytic applications.Key words: chiral ligands, ligand design, oxazolines, variable temperature NMR spectroscopy, asymmetric catalysis, coordination compounds, palladium, platinum
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Tesis sobre el tema "Ligands – Synthesis"

1

Baylies, Christian John. "Synthesis of multidentate pyridyl-thiazole ligands and ligand recognition studies". Thesis, University of Huddersfield, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.399824.

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Chen, Yang. "The syntheses and reactivity of polydentate PNNP ligands and macrocyclic polyphosphine ligands". HKBU Institutional Repository, 1998. http://repository.hkbu.edu.hk/etd_ra/220.

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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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Hassan, Hani Mutlak Abdullah. "Chemical Synthesis of Protein Ligands". Thesis, University of Manchester, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.501975.

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Devlin, Edward Charles. "New ligands for asymmetric synthesis". Thesis, University of Liverpool, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.428366.

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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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Daubinet, André. "Design, synthesis and evaluation of silver-specific ligands". Thesis, Rhodes University, 2001. http://hdl.handle.net/10962/d1004966.

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Several series of ligands, designed to chelate silver(I) specifically in the presence of base metals, have been synthesised. The ligands include: - dithiodiamide compounds, prepared by the condensation of acetanilide derivatives with 1,2-dibromoethane; propanenitrile and propanoic ester derivatives prepared from pyridine-2-carbaldehyde via the Morita-Baylis-Hillman reaction; and novel malonamide ligands from the reaction of diethyl malonate with a range of primary amines. The malonamide derivatives were prepared under both conventional thermal and microwave-assisted conditions, the latter proving to be highly efficient. The ligands were all characterised using a combination of spectroscopic and, where appropriate, elemental analysis; in one case, the structural assignment was confirmed by single-crystal X-ray analysis. The fragmentation patterns in the electron-impact mass spectra of the malonamide derivatives have been explored using high-resolution and meta-stable peak scanning techniques. Complexes of the malonamide ligands with copper(II) and silver(I) have been synthesised, and examination of these complexes has revealed distinct differences in their co-ordination preferences towards silver(I) and copper(II). Tentative, computer-modelled structures for the complexes have been proposed using the available spectroscopic and elemental analysis data. Computer modelling, at the Molecular Mechanics level, has also been used to assess the capacity of the ligand systems to adopt conformations suitable for the chelation of tetrahedral silver(I). Solvent extraction studies have been undertaken using aqueous metal ion solutions and various organic solvents. The dithiodiamide derivatives typically presented solubility problems, but one of the ligands, N,N´-bis(3-chlorophenyl)-3,6-dithiaoctanediamide, exhibited significant but slow extraction of silver(I) into toluene. The malonamide derivatives, however, proved to be readily soluble in ethyl acetate and, in some cases, exhibited good to excellent selectivity for silver(I) in the presence of the base metals copper and lead. Atomic absorption analysis revealed rapid equilibration times (<15 min) and high extraction efficiencies over a wide pH range (2.78 - 9.0). Metal selectivity has been determined by ICP-MS analysis of the residual silver, copper and lead present in the aqueous phase after 15 min, and one of the ligands, N,N´-bis(2-benzylsulfanylethyl)malonamide, exhibits excellent (≥ 96 %) silver(I) specificity.
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Gxoyiya, Babalwa Siliziwe Blossom. "Synthesis and evaluation of PGM-selective ligands". Thesis, Rhodes University, 2013. http://hdl.handle.net/10962/d1007849.

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A series of polydentate POM-selective, sulfur-containing amide ligands have been synthesized from ro-dibromoalkanes and mercaptoacetanilide, The resulting 3,6- dithiaoctanediamides and 3,7-dithianonanediamides, some of which contain a polymerisable group, were all characterized by high-resolution MS, IR, I Hand I3C NMR spectroscopic methods. Various approaches to the polymerisable ligands were explored, the most efficient proving to be the incorporation of an allyl ether moiety in the mercaptoacetanilide. The corresponding Pd(U) and Pt(II) complexes were also prepared from the metal chloride salts and characterized by elemental analysis and spectroscopic methods. The NMR data indicates that both the cis- and transcomplexes were formed, while the IR data indicates cis- coordination of the chlorine . ligands. Molecularly imprinted polymers (MIP's), prepared using platinum(II) mercaptoacetanilide and 3,6-dithiadiamide complexes, showed high selectivity for , , palladium(II) [in the presence of Pt(II), CoCII), Cu(II) and Ni(II)] as determined by . ICP-MS analysis. The more kinetically inert Pt(II) ions however, slowly displaced Pd(II), confirming the Pt(II) selectivity of the MIP's. Solvent extraction studies were conducted to explore the selectivity of the 3,6- dithiaoctanediamides and 3,7-dithianonanediamides for Pd(U) over CoCII), Cu(U) and Ni(II). The ICP-MS data indicate that, in general, equilibration was achieved within ten minutes and that the longer-chain amides were less selective than the shorter-chain analogues.
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Macedo, Emmanuel. "Oxaline-containing ligands : synthesis and applications". Doctoral thesis, KTH, Chemistry, 1998. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-2721.

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Sanchez, Perucha Alejandro. "Novel synthesis of tripodal borate ligands". Thesis, University of Edinburgh, 2007. http://hdl.handle.net/1842/6575.

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Poly(azolyl)borate ligands have proven to be extremely popular ligands since their introduction by Trofimenko in the late 60´s. The basic skeleton of these ligands involves usually three heterocycle units linked to a central boron apex via the azole nitrogen atoms. These ligands have been applied in diverse research areas such as homogeneous catalysis, materials science and bio-inorganic chemistry. More than 2000 papers, including books and reviews regarding the properties of these compounds, have been published. However, only a few synthetic methods for the preparation of such ligands have been reported and only a few examples of chiral borate-centred ligands are known. This thesis deals with the development of a novel synthetic route to tripodal borate ligands using B(NMe2)3 as the boron source. The mechanism of the reaction of this borane with azole heterocycles has been established by exploring the reactivity of a range of azoles. One of the major features of this new synthetic protocol is that it allows the formation of chiral tripodal ligands where the chiral groups are located either at the forth position at the boron atom or at the azole heterocycles. Coordination studies of the ligands have been undertaken and the metal complexes have been studied by a combination of spectroscopic and X- ray diffraction techniques. Preliminary application of the most representative ligands in the Asymmetric Transfer Hydrogenation (ATH) of prochiral ketones has been undertaken in collaboration with Prof. Dieter Vogt at the Technical University of Eindhoven.
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Libros sobre el tema "Ligands – Synthesis"

1

Lappas, Christina. Synthesis of N/N bidentate ligands. Sudbury, Ont: Laurentian University, 1997.

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Cavallin, Anthony. Synthesis of N/N bidentate ligands. Sudbury, Ont: Laurentian University, 1995.

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Chiral auxiliaries and ligands in asymmetric synthesis. New York: Wiley, 1995.

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Mary, McCarthy. Asymmetric catalysis using axially chiral phosphinamine ligands. Dublin: University College Dublin, 1999.

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Farrell, Annette. Asymmetric catalysis using Phosphinamine and Diamine ligands containing a trans-2,5-Dialkylpyrrolidinyl unit. Dublin: University College Dublin, 1999.

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Pellissier, Hélène. Chiral sulfur ligands: Asymmetric catalysis. Cambridge: Royal Society of Chemistry, 2009.

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Higgs, Timothy Charles. Synthesis of polyimidazole ligands and their copper complexes. Manchester: University of Manchester, 1994.

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Shirran, Colette. Novel sulfur ligands for palladium catalysis. Dublin: University College Dublin, 1998.

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Malone, Yvonne M. The preparation and application of diphenylphosphinoferrocenyloxazoline ligands in asymmetric catalysis. Dublin: University College Dublin, 1998.

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Lakes, Aisling M. Novel diamine and phosphinamine ligands and their application in asymmetric catalysis. Dublin: University College Dublin, 1997.

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Capítulos de libros sobre el tema "Ligands – Synthesis"

1

Lefort, Laurent y Johannes G. de Vries. "Phosphoramidite Ligands". En Phosphorus(III) Ligands in Homogeneous Catalysis: Design and Synthesis, 133–57. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9781118299715.ch4.

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Müller, Christian. "Phosphinine Ligands". En Phosphorus(III) Ligands in Homogeneous Catalysis: Design and Synthesis, 287–307. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9781118299715.ch8.

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Hu, Xiang-Ping y Zhuo Zheng. "Bidentate Ligands for Enantioselective Enamide Reduction". En Chiral Amine Synthesis, 273–98. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527629541.ch9.

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Samuels, Michiel C., Bert H. G. Swennenhuis y Paul C. J. Kamer. "Solid-phase Synthesis of Ligands". En Phosphorus(III) Ligands in Homogeneous Catalysis: Design and Synthesis, 463–79. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9781118299715.ch16.

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Bayardon, Jérôme y Sylvain Jugé. "P-Chiral Ligands". En Phosphorus(III) Ligands in Homogeneous Catalysis: Design and Synthesis, 355–89. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9781118299715.ch12.

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Pringle, Paul G. y Martin B. Smith. "Phosphatrioxa-Adamantane Ligands". En Phosphorus(III) Ligands in Homogeneous Catalysis: Design and Synthesis, 391–404. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9781118299715.ch13.

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Tannert, René y Andreas Pfaltz. "Mixed Donor Ligands". En Phosphorus(III) Ligands in Homogeneous Catalysis: Design and Synthesis, 233–65. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9781118299715.ch6.

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Zhou, Qin-Lin y Jian-Hua Xie. "Enantioselective Hydrogenation of Enamines with Monodentate Phosphorus Ligands". En Chiral Amine Synthesis, 247–71. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527629541.ch8.

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Brandsma, L., H. D. Verkruijsse y S. F. Vasilevsky. "Catalysts, Ligands and Reagents". En Application of Transition Metal Catalysts in Organic Synthesis, 1–17. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-60328-0_1.

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Marson, Angelica, Piet W. N. M. van Leeuwen y Paul C. J. Kamer. "Calixarene-Based Phosphorus Ligands". En Phosphorus(III) Ligands in Homogeneous Catalysis: Design and Synthesis, 405–26. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9781118299715.ch14.

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Actas de conferencias sobre el tema "Ligands – Synthesis"

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Zaid, Nurzati Amani Mohamed, Nur Hasyareeda Hassan y Nurul Huda Abd Karim. "Synthesis and characterization β-ketoamine ligands". En THE 2017 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the University Kebangsaan Malaysia, Faculty of Science and Technology 2017 Postgraduate Colloquium. Author(s), 2018. http://dx.doi.org/10.1063/1.5028012.

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Cristalli, Gloria, Diego Dal Ben, Catia Lambertucci, Floriana R. Portino, Sara Taffi, Sauro Vittori y Rosaria Volpini. "Synthesis of new P2 receptor ligands". En XIIIth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2005. http://dx.doi.org/10.1135/css200507087.

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Castro, Guilherme V. de, Vitor Lacerda Sanches, Paulo M. Donate, Igor Polikarpov y Mirela I. de Sairre. "Synthesis of ligands for nuclear receptors of thyroid hormones". En 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013818233325.

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Soares, 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.

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Matiello, Gabriela I., Jairton Dupont y Günter Ebeling. "Synthesis of new ionophilic SNS ligands and their Ru(II) complexes". En 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013101419583.

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Fernández-Figueiras, Adolfo, Fátima Lucio, Paula Munín, Francisco Reigosa, Jose Vila, Maria Pereira y Paula Polo. "SYNTHESIS OF IMINOPHOSPHORANES AS LIGANDS FOR ORGANOMETALLIC COMPOUNDS". En The 20th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a016.

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Wosch, Celso L., Francisco A. Marques, Gustavo Frensch, Ricardo Labes, Beatriz Helena L. N. Sales Maia, Cesar A. Lenz y Palimecio G. Guerrero Jr. "Chiral -Hydroxyalkyloxazolines as Ligands in the Enantioselective Addition of Diethylzinc to Aldehydes". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0251-1.

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Palopoli, Stephen F. y Thomas B. Brill. "Synthesis And Thermolysis Of Metal Complexes Containing Energetic Ligands". En 1988 Los Angeles Symposium--O-E/LASE '88, editado por Joseph Flanagan. SPIE, 1988. http://dx.doi.org/10.1117/12.943744.

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Quinteros, Gisela J. y Sandra E. Martín. "Synthesis of biphenyl-based arsine ligands by microwaveassisted Suzuki-Miyaura coupling and their applications". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0162-1.

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Karlsson, Erik A., Jèssica Margalef, Javier Mazuela, Òscar Pàmies, Montserrat Diéguez y Miquel A. Pericàs. "P,S-ligands for Ir-catalyzed Asymmetric Hydrogenation of Minimally Functionalized Olefins – A Theoretical Study". En 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013913152358.

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Informes sobre el tema "Ligands – Synthesis"

1

Su, Ning, Jerald S. Bradshaw, Paul B. Savage, Krzysztofe E. Krakowiak y Reed M. Izaft. Synthesis and Aggregate Study of Bisphenol-Containing Diaza- 18-Crown-6 Ligands. Fort Belvoir, VA: Defense Technical Information Center, septiembre de 1999. http://dx.doi.org/10.21236/ada368629.

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Shriver, D. F. Synthesis, Structures and Spectroscopy of Metal Clusters Containing Polycarbon and Heterocumulene Ligands. Office of Scientific and Technical Information (OSTI), julio de 2000. http://dx.doi.org/10.2172/763379.

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Su, Ning, Jerald S. Bradshaw, Paul B. Savage, Guoping Xue, Krzysztof E. Krakowiak y Reed M. Izaft. Synthesis of Novel 8-Hydroxyquinoline-Containing Diaz-18-Crown-6 Ligands and Analogues. Fort Belvoir, VA: Defense Technical Information Center, noviembre de 1999. http://dx.doi.org/10.21236/ada370492.

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Long, Brian K. STIR: Redox-Switchable Olefin Polymerization Catalysis: Electronically Tunable Ligands for Controlled Polymer Synthesis. Fort Belvoir, VA: Defense Technical Information Center, marzo de 2013. http://dx.doi.org/10.21236/ada579827.

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Beasley, Jonathan. Synthesis of heterocycles: Indolo (2,1-a) isoquinolines, renewables, and aptamer ligands for cellular imaging. Office of Scientific and Technical Information (OSTI), enero de 2013. http://dx.doi.org/10.2172/1082980.

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Clearfield, Abraham. The Synthesis, Structures, and Chemical Properties of Macrocyclic Ligands Covalently Bonded into Layered Arrays. Office of Scientific and Technical Information (OSTI), noviembre de 2014. http://dx.doi.org/10.2172/1164084.

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Abraham Clearfield. The Synthesis, Structures and Chemical Properties of Macrocyclic Ligands Covalently Bonded into Layered Arrays. Office of Scientific and Technical Information (OSTI), julio de 2009. http://dx.doi.org/10.2172/959123.

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Schultz, Madeleine. Synthesis and structure of bivalent ytterbocenes and their coordination chemistry with pi-acceptor ligands. Office of Scientific and Technical Information (OSTI), mayo de 2000. http://dx.doi.org/10.2172/764392.

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Wang, Chia-Mei. Synthesis and reactivity of Ru complexes with dibenzothiophene and hexahydrodibenzothiophene ligands: Models for catalytic hydrodesulfurization. Office of Scientific and Technical Information (OSTI), febrero de 1990. http://dx.doi.org/10.2172/6945225.

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Bronson, R. T., Jerald S. Bradshaw, Paul B. Savage, Krzysztof E. Krakowiak y Reed M. Izatt. Synthesis of Bis-8-Hydroxyquinoline-Armed Diazatrithia-15-Crown-5 and Diazatrithia-16-Crown-5 Ligands. Fort Belvoir, VA: Defense Technical Information Center, abril de 2001. http://dx.doi.org/10.21236/ada389716.

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