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Relevant bibliographies by topics / Palladacycles

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Academic literature on the topic 'Palladacycles'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 September 2023

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Journal articles on the topic "Palladacycles"

1

Ostrowska, Sylwia, Lorenzo Palio, Agnieszka Czapik, et al. "A Second-Generation Palladacycle Architecture Bearing a N-Heterocyclic Carbene and Its Catalytic Behavior in Buchwald–Hartwig Amination Catalysis." Catalysts 13, no. 3 (2023): 559. http://dx.doi.org/10.3390/catal13030559.

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Palladacyclic architectures have been shown as versatile motifs in cross-coupling reactions. NHC-ligated palladacycles possessing unique electronic and steric properties have helped to stabilize the catalytically active species and provide additional control over reaction selectivity. Here, we report on a synthetic protocol leading to palladacycle complexes using a mild base and an environmentally desirable solvent, with a focus on complexes bearing backbone-substituted N-heterocyclic carbene ligands. The readily accessible complexes exhibit high catalytic activity in the Buchwald–Hartwig amination. This is achieved using low catalyst loading and mild reaction conditions in a green solvent.

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Zhang, Yanghui, Bo Zhou, and Ailan Lu. "Pd-Catalyzed C–H Silylation Reactions with Disilanes." Synlett 30, no. 06 (2018): 685–93. http://dx.doi.org/10.1055/s-0037-1610339.

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Pd-catalyzed C–H silylation reactions remain underdeveloped. General strategies usually rely on the use of complex bidentate directing groups. C,C-Palladacycles exhibit extremely high reactivity towards hexamethyldisilane and can be disilylated very efficiently. The C,C-palladacycles are prepared through halide-directed C–H activation. This account introduces Pd-catalyzed C–H silylation reactions with disilanes as the silyl source, and is focused on studies on the silylation of C,C-palladacycles.1 Introduction and Background2 Allylic C–H Silylation Reaction3 Coordinating-Ligand-Directed C–H Silylation Reaction4 Disilylation of C(sp2),C(sp2)-Palladacycles That are Generated by C(sp2)–H activation5 Disilylation of C(sp2),C(sp3)-Palladacycles That are Generated by C(sp3)–H Activation6 Disilylation of C,C-Palladacycles That are Generated through Domino Processes7 Summary and Outlook

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Rúa-Sueiro, Marcos, Paula Munín-Cruz, Adolfo Fernández, Juan M. Ortigueira, María Teresa Pereira, and José M. Vila. "Cyclometallated Palladium(II) Complexes: An Approach to the First Dinuclear Bis(iminophosphorane)phosphane-[C,N,S] Metallacycle." Molecules 27, no. 20 (2022): 7043. http://dx.doi.org/10.3390/molecules27207043.

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Treatment of bis(iminophosphorane)phosphane ligands 2a–2e with Li2PdCl4 gave a set of novel diphosphane-derived complexes bearing two metallacycle rings, each one enclosing a P=N double bond: the unprecedented bis(iminophosphorane)phosphane-[C,N,S] palladacycles. In the case of the ligand derived from bis(diphenylphosphino)methane, 2a, both the single and the double palladacycle complexes were obtained. Reaction of 3a with bis(diphenylphosphino)ethane did not yield the expected product with the diphosphane bonded to both palladium atoms, but rather the novel coordination compound 5. The crystal structures of 3c and 5 are described.

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Catellani, Marta. "Selective organometallic syntheses from molecular pools." Pure and Applied Chemistry 74, no. 1 (2002): 63–68. http://dx.doi.org/10.1351/pac200274010063.

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A new methodology is described, consisting of the use of molecular pools in palladium-catalyzed sequential processes occurring under mild conditions with high selectivity. These reactions involve palladacycle formation from aryl iodide, palladium, and norbornene, the latter behaving as a second catalyst that is first incorporated into the metallacycle and expelled at the end of the process. Selective alkylation or arylation of the arene nucleus occurring by oxidative addition/reductive elimination of palladacycles are coupled, after norbornene expulsion, with CH or CC bond-forming reactions such as hydrogenolysis, olefin insertion, arylboronic coupling, etc. The variety of possible combinations offers a powerful tool for the selective synthesis of unusual and not readily accessible aromatics.

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Roffe, Gavin W., Sarote Boonseng, Christine B. Baltus, et al. "A synthetic, catalytic and theoretical investigation of an unsymmetrical SCN pincer palladacycle." Royal Society Open Science 3, no. 4 (2016): 150656. http://dx.doi.org/10.1098/rsos.150656.

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The SCN ligand 2-{3-[(methylsulfanyl)methyl]phenyl}pyridine, 1, has been synthesized starting from an initial Suzuki–Miyaura (SM) coupling between 3-((hydroxymethyl)phenyl)boronic acid and 2-bromopyridine. The C–H activation of 1 with in situ formed Pd(MeCN) 4 (BF 4 ) 2 has been studied and leads to a mixture of palladacycles, which were characterized by X-ray crystallography. The monomeric palladacycle LPdCl 6, where L-H = 1, has been synthesized, and tested in SM couplings of aryl bromides, where it showed moderate activity. Density functional theory and the atoms in molecules (AIM) method have been used to investigate the formation and bonding of 6, revealing a difference in the nature of the Pd–S and Pd–N bonds. It was found that S-coordination to the metal in the rate determining C–H bond activation step leads to better stabilization of the Pd(II) centre (by 13–28 kJ mol −1 ) than with N-coordination. This is attributed to the electron donating ability of the donor atoms determined by Bader charges. The AIM analysis also revealed that the Pd–N bonds are stronger than the Pd–S bonds influencing the stability of key intermediates in the palladacycle formation reaction pathway.

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-S.S.H. Elgazwy, A., N. S.M. Ismail, S. R. Atta-Allah, et al. "Palladacycles as Antimicrobial Agents." Current Medicinal Chemistry 19, no. 23 (2012): 3967–81. http://dx.doi.org/10.2174/092986712802002527.

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7

Dyker, Gerald. "Palladacycles as Reactive Intermediates." Chemische Berichte 130, no. 11 (1997): 1567–78. http://dx.doi.org/10.1002/cber.19971301104.

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Dyker, Gerald. "Palladacycles as Reactive Intermediates." European Journal of Inorganic Chemistry 1998, no. 6 (1998): 877. http://dx.doi.org/10.1002/(sici)1099-0682(199806)1998:6<877::aid-ejic877>3.0.co;2-6.

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9

Roffe, Gavin W., Graham J. Tizzard, Simon J. Coles, Hazel Cox, and John Spencer. "Synthesis of unsymmetrical NCN′ and PCN pincer palladacycles and their catalytic evaluation compared with a related SCN pincer palladacycle." Organic Chemistry Frontiers 3, no. 8 (2016): 957–65. http://dx.doi.org/10.1039/c6qo00198j.

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Ji, Xiaoming, Feng Wei, Bin Wan, Cang Cheng, and Yanghui Zhang. "Palladium-catalyzed intermolecular C–H silylation initiated by aminopalladation." Chemical Communications 56, no. 56 (2020): 7801–4. http://dx.doi.org/10.1039/d0cc00872a.

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Dissertations / Theses on the topic "Palladacycles"

1

Holuigue, Alexandre. "Palladacycles : synthesis and catalysis." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2008. http://dare.uva.nl/document/96898.

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Swarts, Andrew John. "Mononuclear and multinuclear palladacycles as catalysts." Thesis, Stellenbosch : University of Stellenbosch, 2011. http://hdl.handle.net/10019.1/6626.

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Cazin, Catherine Suzanne Julienne. "Catalysis of carbon-carbon and carbon-heteroatom bond-forming reactions : the importance of the palladium source." Thesis, University of Exeter, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.248165.

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Mancilha, Fabiana Szczesny. "Benzothiadiazoles: synthesis, photophysical and biological properties and palladacycles." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2010. http://hdl.handle.net/10183/26316.

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Le travail présenté dans ce memoire a été realisé au Laboratory of Molecular Catalysis (Chapitre 1, 2 et 3) de l'Universidade Federal do Rio Grande do Sul, sous la direction du Prof. Jaïrton Dupont, et au Laboratoire de Synthèse Métallo Induites (Chapitre 4) de l'Université de Strasbourg, sous la direction du Dr. Michel Pfeffer, entre le mois d'Aoüt 2006 et le mois de Décembre 2009. Le présent travail décrit la synthese et la caracterisation de nouvelles molecules п-extensibles contenant le noyau 2,1,3-benzothiadiazole (BID) et ses derives. Nous avons fait ('extension п des positions 4 et 7 de la BTD en utilisant les reactions de Suzuki et Sonogashira avec de bons rendements. Nous avons aussi bien caracterise ces nouveaux composes et etudie leurs caracteristiques electrochimiques et photophysiques. Nous avons étudié ('application des derives non symetriques de la BTD pour ('intercalation avec l'ADN. Pour les tests avec l'ADN, nous avons choisi trois composes ayant pour caractéristique commune un noyau BTD portant un groupe 4- methoxyphenyle, et dont nous avons fait varier la nature du substituant en position 7 : pyridine (2 et 3-pyridine) ou phenyle. Ces molécules ont donné d'excellents résultats lors de l'étude de leurs propriétés d'intercalation et de leurs propriétés photophysiques. Des nouvelles molécules cyclométallées ont été obtenues par la réaction des dérivés BTD avec l'acetate de palladium. Une série de complexes cyclopallades a pu être préparée avec de très bons rendements, sans que I'atome de soufre n'interagisse avec le metal. II est remarquable qu'il s'agisse de metallacycles a 6 chainons, moins courants que ceux a 5 chaînons. Tous les complexes ont 6t6 completement caractériéss, notamment par analyse élémentaire et par spectroscopie RMN, IR et UV-visible. Certains d'entre eux ont cristallises, et les monocristaux correspondants ont été analysés par diffraction des Rayons-X.<br>The present work was carried out at the Laboratory of Molecular Catalysis (Chapters 1, 2 and 3) in the Universidade Federal do Rio Grande do Sul, under supervision of Prof. JaIrton Dupont, and at the Laboratoire de Syntheses Metallo Induites (Chapter 4) at the Universite de Strasbourg, under supervision of Prof. Michel Pfeffer, between August 2006 and December 2009. In this work we describe the synthesis and characterisation of new Tr-extended molecules with the 2,1,3-benzothiadiazole core and their derivatives. We have performed the u extension of 4 and 7 positions of the BTD core employing Suzuki and Sonogashira reaction with good yields. The new molecules were fully characterized and their electrochemical and photophysical properties were investigated. Intercalation of the non symmetrical BTD derivatives and DNA were studied. Three molecules were chosen for testing the DNA intercalation, all compounds with the 4-methoxyphenyl group as the common ligand bound to one side of BTD core and a pyridine (2- or 3-pyridine) or a phenyl to the other side. We obtained excellent results for the intercalation and photophysical properties. New cyclometallated compounds were obtained by the reaction of palladium acetate and the BTD derivatives. A series of cyclopalladated compounds were synthesized with good yields with no interaction between the metal and sulphur atom. The remarkable characteristic of these cyclometallated compounds is the formation of 6 member rings, less commons than 5 members rings. All compounds were fully characterized by elemental analysis and NMR spectroscopy, IR and UV-Vis. Some complex were crystallized and analyzed by X-Ray diffraction.

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Szczesny, Mancilha Fabiana. "Benzothiadiazoles : synthesis, photophysical and biological properties and palladacycles." Strasbourg, 2010. http://www.theses.fr/2010STRA6061.

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Le travail présenté dans ce mémoire a été réalisé au Laboratory of Molecular Catalysis (Chapitre 1, 2 et 3) de l'Universidade Federal do Rio Grande do Sul, sous la direction du Prof. Jaïrton Dupont, et au Laboratoire de Synthése Métallo Induites (Chapitre 4) de l'Université de Strasbourg, sous la direction du Dr. Michel Pfeffer, entre le mois d'Août 2006 et le mois de Décembre 2009. Le présent travail décrit la synthèse et la caractérisation de nouvelles molécules TT-extensibles contenant le noyau 2,1 ,3-benzothiadiazole (BTD) et ses dérivés. Nous avons étudié l'application des dérivés non symétriques de la BTD pour l'intercalation avec l'ADN. Pour les tests avec l'ADN, nous avons choisi trois composés ayant pour caractéristique commune un noyau BTD portant un groupe 4-méthoxyphényle, et dont nous avons fait varier la nature du substituant en position 7: pyridine (2 et 3-pyridine) ou phényle. Ces molécules ont donné d'excellents résultats lors de l'étude de leurs propriétés d'intercalation et de leurs propriétés photophysiques. Des nouvelles molécules cyclométallées ont été obtenues par la réaction des dérivés BTD avec l'acétate de palladium. Une série de complexes cyclopalladés a pu être préparée avec de très bons rendements, sans que l'atome de soufre n'interagisse avec le métal. Il est remarquable qu'il s'agisse de métallacycles à 6 chaînons, moins courants que ceux à 5 chaînons. Tous les complexes ont été complètement caractérisés, notamment par analyse élémentaire et par spectroscopie RMN, IR et UV-visible. Certains d'entre eux ont cristallisés, et les monocristaux correspondants ont été analysés par diffraction des Rayons-X<br>The present work was carried out at the Laboratory of Molecular Catalysis (Chapters 1,2 and 3) in the Universidade Federal do Rio Grande do Sul, under supervision of Prof. Jaïrton Dupont, and at the Laboratoire de Synthèses Métallo Induites (Chapter 4) at the Université de Strasbourg, under supervision of 1 Prof. Michel Pfeffer, between August 2006 and December 2009. ) ln this work we describe the synthesis and characterisation of new TT-extended molecules with the 2,1 ,3-benzothiadiazole core and their derivatives. We have performed the TT extension of 4 and 7 positions of the BTD core employing Suzuki and Sonogashira reaction with good yields. The new molecules were fully characterized and their electrochemical and photophysical properties were investigated. Intercalation of the non symmetrical BTD derivatives and DNA were studied. Three molecules were chosen for testing the DNA intercalation, ail compounds with the 4-methoxyphenyl group as the common ligand bound to one side of BTD core and a pyridine (2- or 3-pyridine) or a phenyl to the other side. VJ. E obtained excellent results for the intercalation and photophysical properties. New cyclometallated compounds were obtained by the reaction of palladium acetate and the BTD derivatives. A series of cyclopalladated compounds were synthesized with good yields with no interaction between the metal and sulphur atom. The remarkable characteristic of these cyclometallated compounds is the formation of 6 member rings, less commons than 5 members rings. Ali compounds were fully characterized by elemental analysis and NMR spectroscopy, IR and UV-Vis. Sorne complex were crystallized and analyzed by X-Ray diffraction

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6

Kozlik, Roza Maria. "The chemistry of palladacycles derived from phenyl-oxazolines /." abstract and full text PDF (UNR users only), 2007. http://0-gateway.proquest.com.innopac.library.unr.edu/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:3279641.

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Thesis (Ph. D.)--University of Nevada, Reno, 2007.<br>"May, 2007." Includes bibliographical references. Library also has microfilm. Ann Arbor, Mich. : ProQuest Information and Learning Company, [2008]. 1 microfilm reel ; 35 mm. Online version available on the World Wide Web.

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7

Pilarski, Lukasz T. "Palladacycles for non-redox C-C bond forming reactions." Thesis, University of Bristol, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.495644.

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This thesis is concerned with the use of palladacyclic complexes as catalysts for C-C and C-heteroatom bond-forming reactions in which an oxidation state change of the metal centre is not part of the catalytic cycle. To this end, the investigation of a range of known K²-C,L-based palladacycles in the allylation of aldehyde and imine substrates using stannanes, as well as the 1,4-conjugate arylation of enones and imines using arylboronic acids under mild conditions is described. In each case the commercially available phosphite-based dimeric palladacycle is found to be the most active complex capable of achieving excellent conversions (>90%) at the 0.5 - 2.5mol% loading range. Three previously unknown phosphinite and amidophosphinite palladium pincer complexes are also synthesised, characterised (including crystallographically) and tested in the 1,4-conjugate addition of phenylboronic acid to chalcone and found to be inactive.

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8

Boonseng, Sarote. "Computational study of the reactivity of palladacycles in catalytic applications." Thesis, University of Sussex, 2017. http://sro.sussex.ac.uk/id/eprint/68416/.

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This thesis presents a detailed theoretical/computational analysis using quantum chemistry to investigate the thermochemistry and reaction mechanisms of palladacycles that underpin experimental observations. The thesis begins by establishing a suitable computational methodology for the study of pincer palladacycles. It was found that Density Functional Theory (DFT) was suitable for the accurate reproduction of geometric structures and energetics by comparing a range of commonly used density functionals and basis sets with the X-ray crystal structures of symmetric pincer palladacycles. The detailed electronic structure of several pincer palladacycles was investigated using Complete Active Space Self-Consistent Field method (CASSCF) and it was shown that the dominant configuration was larger than 0.96, indicating that the ground state electronic structure has significant single-reference character. DFT was used to investigate the stability of symmetrical pincer palladacycles, and then by changing the donor ligand, unsymmetrical pincer palladacycles. The pincer palladacycle formation was investigated and it was found that the barrier to C-H activation was dependent on the ligand arm of the pincer that coordinates to PdCl2. Topological analysis was performed using Quantum Theory of Atoms In Molecules (QTAIM) for determining the strength and nature of the Pd and donor atom interactions, showing that the bond strength depends on the type of donor atom and trans influence in the pincer palladacycles. The mechanism for Pd(0) formation from both symmetrical and unsymmetrical pincer palladacycle pre-catalysts for catalysis in Suzuki-Miyaura carbon-carbon cross-coupling reactions was studied, and then with the introduction of base and the effect of solvent. It was shown that the key steps are transmetallation and reductive elimination processes, and differences in the overall Gibbs free energy and transmetallation barrier provide an explanation for observed catalytic activity. This has been in conjunction with experimental chemists. Finally, the functionalisation of benzodiazepines was investigated in three conditions; with Pd(II)/Ru(II)-catalysts, with Pd(II)-catalysts and without catalyst. It was found that the Ru(II) photocatalyst with Pd(II)-catalyst is the best condition for functionalisation on benzodiazepines with the lowest energy barrier.

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Roffe, Gavin William. "The synthesis, catalytic investigation, and theoretical rationalisation of unsymmetrical pincer palladacycles." Thesis, University of Sussex, 2016. http://sro.sussex.ac.uk/id/eprint/63061/.

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This thesis presents the synthesis of a number of unsymmetrical SCN, N'CN, PCN and PCS pincer palladacycles. A new synthetic route has been designed towards unsymmetrical pincer ligands, involving a key Suzuki-Miyaura coupling, yielding the characteristic biaryl ligand backbone presented. New unsymmetrical SCN pincer ligands, containing a pyridine and a thioether ligand were synthesised. A number of substituents were used on the thioether ligand arm, with various steric demand and electron donating characteristics. These unsymmetrical ligands underwent C-H bond activation with palladium (II) salts, yielding the corresponding palladacycles. In order to investigate the effect of changing the sulphur donor atom, the thioether ligand arm was replaced by amines in the synthesis of N'CN pincer palladacycles, and phosphinites in the synthesis of PCN pincer palladacycles. Also changing the pyridine donor arm to a thioether was investigated, yielding a PCS pincer palladacycle. The palladacycles were tested in a number of catalytic applications: Suzuki-Miyaura coupling of sterically demanding and electronically deactivated aryl bromides; cross coupling of arylboronic acids and vinyl epoxides; and catalytic aldol condensations; revealing differences between the SCN, N'CN and PCN pincer palladacycles. In order to investigate the differences in catalytic activity, density functional theory was employed. A palladacycle formation pathway containing a key C-H bond activation step was investigated for an SCN pincer palladacycle, revealing differences in energy barriers of the C-H bond activation step depending on whetherthe thioether or the pyridine arm coordinates to the PdCl2 first. Next, the activation pathway of the palladacycles in the Suzuki-Miyaura coupling reaction was studied, identifying key transmetallation and reductive elimination steps. Differences in the overall thermodynamics and kinetics provide explanations for differences in catalytic activity. The results show that slower release of the catalytically active Pd(0) species yield a better precatalyst in the Suzuki-Miyaura coupling reaction, due to the lower propensity to form catalytically inactive palladium black. Overall this thesis provides a novel synthetic route to a family of unsymmetrical pincer palladacycles; their testing in catalytic activity in several applications, revealing differences in catalytic activity; and a theoretical study into key mechanisms, C-H bond activation, and catalyst activation in the Suzuki-Miyaura coupling reaction, which provide a rationalisation to the varying catalytic activities of the unsymmetrical pincer palladacycles.

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Fischer, Daniel Friedrich. "New frontiers in asymmetric aza-Claisen rearrangements : development of ferrocenyl imidazoline palladacycles /." [S.l.] : [s.n.], 2008. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=18128.

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Books on the topic "Palladacycles"

1

Pfeffer, Michel, and Jairton Dupont. Palladacycles: Synthesis, characterization and applications. Wiley-VCH, 2008.

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Palladacycles. Elsevier, 2019. http://dx.doi.org/10.1016/c2017-0-03671-6.

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Dupont, Jairton, and Michel Pfeffer, eds. Palladacycles. Wiley, 2008. http://dx.doi.org/10.1002/9783527623211.

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Maiti, Debabrata, and Anant Kapdi. Palladacycles: Catalysis and Beyond. Elsevier Science & Technology Books, 2019.

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Maiti, Debabrata, and Anant Kapdi. Palladacycles: Catalysis and Beyond. Elsevier, 2019.

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Palladacycles Synthesis Characterization And Applications. Wiley-VCH Verlag GmbH, 2008.

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Pfeffer, Michel, and Jairton Dupont. Palladacycles: Synthesis, Characterization and Applications. Wiley & Sons, Incorporated, John, 2008.

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Book chapters on the topic "Palladacycles"

1

Dyker, Gerald. "Polycyclic Ring Systems via Palladacycles as Reactive Intermediates." In Organic Synthesis via Organometallics OSM 5. Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-49348-5_9.

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Vila, José M., M. Teresa Pereira, Fátima Lucio-Martínez, and Francisco Reigosa. "Palladacycles as Efficient Precatalysts for Suzuki-Miyaura Cross-Coupling Reactions." In Palladacycles. Elsevier, 2019. http://dx.doi.org/10.1016/b978-0-12-815505-9.00002-0.

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Choy, Pui Ying, Xinwei He, and Fuk Yee Kwong. "Palladacycles as Precatalysts for Heck and Sonogashira Cross-Coupling Reactions." In Palladacycles. Elsevier, 2019. http://dx.doi.org/10.1016/b978-0-12-815505-9.00003-2.

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Serrano, José L., and Tejpalsingh R. Girase. "Palladacycles as Efficient Precatalysts for Negishi and Buchwald-Hartwig Amination Reactions." In Palladacycles. Elsevier, 2019. http://dx.doi.org/10.1016/b978-0-12-815505-9.00004-4.

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Shaughnessy, Kevin H. "Introduction of Water-Solubility in Palladacycles and Their Catalytic Applications." In Palladacycles. Elsevier, 2019. http://dx.doi.org/10.1016/b978-0-12-815505-9.00005-6.

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Khan, Raysa, and John Spencer. "Palladacyclic Complexes as Efficient Catalysts for C H Bond Functionalization Reactions." In Palladacycles. Elsevier, 2019. http://dx.doi.org/10.1016/b978-0-12-815505-9.00006-8.

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Malinakova, Helena C. "Multicomponent Reaction Sequences Using Palladacyclic Complexes." In Palladacycles. Elsevier, 2019. http://dx.doi.org/10.1016/b978-0-12-815505-9.00007-x.

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Soni, Vineeta, and Benudhar Punji. "Enantioselective Synthesis Using Chiral Palladacycles." In Palladacycles. Elsevier, 2019. http://dx.doi.org/10.1016/b978-0-12-815505-9.00008-1.

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Shah, Jagrut A., and Bhalchandra M. Bhanage. "Nanoparticular or Colloidal Pathways for Palladacycles-Mediated Catalytic Processes." In Palladacycles. Elsevier, 2019. http://dx.doi.org/10.1016/b978-0-12-815505-9.00009-3.

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Bangde, Prachi, Dharmendra Prajapati, Prajakta Dandekar, Ian J. S. Fairlamb, and Anant R. Kapdi. "Palladacycles as Potential Anticancer Agents." In Palladacycles. Elsevier, 2019. http://dx.doi.org/10.1016/b978-0-12-815505-9.00010-x.

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Conference papers on the topic "Palladacycles"

1

Munín, Paula, Francisco Reigosa, Marcos Rúa-Sueiro, Juan Ortigueira, Maria Pereira, and Jose Vila. "Synthesis and characterization of iminophosphorane palladacycles." In The 23rd International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2019. http://dx.doi.org/10.3390/ecsoc-23-06487.

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Rúa-Sueiro, Marcos, Paula Munin-Cruz, Francisco Reigosa, José M. Vila, and M. Teresa Pereira. "Synthesis and characterization of novel thiosemicarbazone palladacycles." In The 23rd International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2019. http://dx.doi.org/10.3390/ecsoc-23-06494.

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Munín, Paula, Francisco Reigosa, Fatima Lucio, et al. "Synthesis and study of the stability of phosphane palladacycles." In The 22nd International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2018. http://dx.doi.org/10.3390/ecsoc-22-05765.

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Munín-Cruz, Paula, Marcos Rúa-Sueiro, Juan Ortigueira, and José Vila. "Synthesis of novel bisiminophosphorane palladacycles with miscellaneous bidentate chelating ligands." In The 24th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecsoc-24-08321.

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Fernández-Figueiras, Adolfo, Fátima Lucio, Francisco Reigosa, et al. "Synthesis of functionalized biaryls using iminophosphorane palladacycles as Suzuki catalysts." In The 21st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04773.

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Rúa-Sueiro, Marcos, Paula Munin-Cruz, Francisco Reigosa, José M. Vila, and Juan M. Ortigueira. "Synthesis and X-ray diffraction study of thiosemicarbazone palladacycles with dppm." In The 2nd International Online Conference on Crystals. MDPI, 2020. http://dx.doi.org/10.3390/iocc_2020-07352.

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Bermudez, Sara, Raquel Diz-Gil, Paula Munín-Cruz, Marcos Rúa-Sueiro, Juan Ortigueira, and José Vila. "Preparation of novel complexes bearing diphosphine (dppm) derived from thiosemicarbazone palladacycles." In The 24th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecsoc-24-08320.

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Janabi, Basma Al, Jose Manuel Vila, and Juan M. Ortigueira. "Palladacycles as Functionalized Metal-Ligand Precursors, Contain Tridentate [Csp2, N, S] Ligands." In ECSOC-25. MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11663.

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Polo-Ces, Paula, Pablo Frieiro-Gomis, Fátima Lucio-Martínez, et al. "Palladacycles derivates of diimines ligands [N,C,C,N]." In The 21st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04760.

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Pinho, Vagner D., Raquel Ana C. Leão, Arthur Serpa Coelho, Arthur Eugen Kümmerle, and Paulo R. R. Costa. "New Palladacycles Derived Acylhydrazones and Hydrazones as Pre-catalyst in Mirozoki-Heck Coupling and Oxyarylations." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0072-2.

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