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1

Weeks, Amanda. "C-H activation in organic synthesis." Thesis, University of Bristol, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.535205.

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2

Doyle, Claire Marie. "C-H activation reactions of tetrahydropyridines." Thesis, Imperial College London, 2012. http://hdl.handle.net/10044/1/9469.

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This thesis is presented as five chapters: Chapter 1.0 is divided into two sections: the first is a review of palladium-catalysed C–C bond forming reactions. It covers palladium-catalysed cross-coupling reactions; C–H bond functionalisation; the Heck reaction and functionalisation of heteroaromatic C–H bonds. Secondly the use of tetrahydropyridines in organic synthesis is discussed, with a particular focus on methodology developed by the Craig group. Chapter 2.0 discusses the research carried out during this studentship. It is divided into six sections and discusses the results obtained from r
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3

Di, Matteo Marco. "Selective C-H Activation of Terpenes." Electronic Thesis or Diss., Sorbonne université, 2024. https://accesdistant.sorbonne-universite.fr/login?url=https://theses-intra.sorbonne-universite.fr/2024SORUS001.pdf.

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Ce travail de thèse porte sur la découverte de nouvelles stratégies pour l'activation/fonctionnalisation C-H des terpènes, avec un accent particulier sur le (+)-limonène et la catalyse au palladium. Tout d'abord, nous avons décrit le couplage C(sp2)-H/C(sp2)-H déshydrogénant catalysé par le Pd(II) entre le limonène et des alcènes pauvres en électrons, avec une extension à divers terpènes et terpénoïdes. Ensuite, nous avons étudié la post-fonctionnalisation d'un produit issu du couplage déshydrogénant développé et de l'éthynylbenzène en conditions micellaires. Par la suite, nous avons développé
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4

Vastine, Benjamin Alan. "Understanding mechanisms for C-H bond activation." [College Station, Tex. : Texas A&M University, 2008. http://hdl.handle.net/1969.1/ETD-TAMU-2679.

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5

Khamker, Qudsia. "Ambiphilic C-H activation routes to heterocycles." Thesis, University of Leicester, 2014. http://hdl.handle.net/2381/28919.

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This thesis describes investigations of Cp*Rh- and (p-Cy)Ru-catalysed C-H functionalisation reactions of various substrates with alkynes and alkenes for the formation of several heterocycles and carbocycles. Mechanistic studies and DFT calculations are also presented. Chapter One includes a discussion of different mechanisms of C-H activation namely oxidative addition, σ-bond metathesis, 1,2-addition, electrophilic activation and AMLA/CMD. The applications of these different mechanisms of C-H activation in catalysis are also discussed with a particular emphasis on the use of AMLA/CMD in direct
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6

Wiley, Jack Scott. "C-H bond activation in iridium complexes /." Thesis, Connect to this title online; UW restricted, 1999. http://hdl.handle.net/1773/8510.

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7

Bu, Qingqing. "Ruthenium- and Cobalt-Catalyzed C-H Activation." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2018. http://hdl.handle.net/11858/00-1735-0000-002E-E4FC-F.

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8

Moselage, Marc Philipp. "C-H and C-C Activation by Cobalt and Ruthenium Catalysis." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2017. http://hdl.handle.net/11858/00-1735-0000-0023-3FB2-6.

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9

Hebert, Alexandra. "Mise au point de nouvelles techniques de radio-iodation et application au radiomarquage de molécules d'intérêt." Thesis, Normandie, 2019. http://www.theses.fr/2019NORMC413/document.

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Le radiomarquage de molécules d’intérêt avec des isotopes radioactifs est d'un grand intérêt pour la communauté scientifique, car il influe fortement sur le processus de découverte dans les sciences de la vie et en médecine nucléaire. Les molécules radiomarquées ont été largement utilisées pour évaluer les réactions biochimiques, pour mesurer la distribution in vivo d'une substance ou pour réaliser des tests RIA (RadioImmunoAssay). En médecine nucléaire, des radiopharmaceutiques pour la thérapie par ra-dio-isotopes (RIT) et des radiotraceurs pour des expériences d'imagerie telles que la TEP (t
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10

Wang, Hui. "Cobalt(III)- and Manganese(I)-Catalyzed C-H and C-C Activations." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2019. http://hdl.handle.net/11858/00-1735-0000-002E-E5EF-5.

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11

Torkelson, Jeffrey Robert. "C-H bond activation and C-C bond formation at adjacent metals." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp03/NQ34848.pdf.

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12

Zhang, Shoukun. "Selective C–H Activation by Ruthenium(II) Carboxylate and Nickelaelectro-Catalysis." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2021. http://hdl.handle.net/21.11130/00-1735-0000-0005-155B-E.

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13

Chow, Catherine. "C-H activation by a tungsten trimethylsilylallyl complex." Thesis, University of British Columbia, 2012. http://hdl.handle.net/2429/42646.

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Thermolysis of Cp*W(NO)(Np)(η³-CH₂CHCHSiMe₃) generates a 16-electron allene intermediate complex that selectively activates hydrocarbons at their methyl groups. In the case of linear alkanes, only terminal activation is observed. This selectivity persists in the presence of an ether functionality, but not of other oxygen-containing substrates such as aldehydes and alcohols. With these latter substrates, oxidation of the complex to Cp*W(O)₂Np has been noted. The existence of the allene intermediate has been verified by two thermolytic experiments, and kinetic studies show that Cp*W(NO)(Np)(η³-
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14

Luo, Junfei. "Controlling regioselectivity and enantioselectivity in C-H activation." Thesis, Queen Mary, University of London, 2015. http://qmro.qmul.ac.uk/xmlui/handle/123456789/9550.

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The direct functionalisation of C-H bonds has emerged in recent years as an efficient and atom-economic alternative to the traditional cross coupling reaction. One of the challenges towards this goal is the selective transformation of a particular C-H bond amongst many other C-H bonds. This thesis describes studies on the use of CO2 as a traceless promoter for controlling meta-regioselective arylation of phenols and a separate investigation into an enantioselective arylation of pre-chiral η6-arene tricarbonyl chromium complexes. The introduction provides a general review of recent advances in
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15

Müller, Thomas. "C-H Activation by Nickel and Iron Catalysis." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2019. http://hdl.handle.net/21.11130/00-1735-0000-0003-C189-8.

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16

Gao, Longhui. "C-H bond activation catalyzed by Ruthenium nanoparticles." Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLS348/document.

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Les molécules marquées par des isotopes de l’hydrogène possèdent de nombreuses applications dans divers domaines tels que la chimie, la biologie ou en science des matériaux. Dans le domaine de la recherche de nouveaux médicaments, les études liées à la pharmacocinétique nécessitent un accès rapide à des molécules marquées afin de ne pas impacter les coûts et les délais de développement. Le développement de la métabolomique a aussi entrainé une augmentation du besoin en molécules marquées isotopiquement. En effet, les molécules deuterées peuvent être utilisées en tant qu’étalons internes pour l
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17

Biswas, Achintesh Narayan. "C-H bond activation by transition metal complexes." Thesis, University of North Bengal, 2010. http://hdl.handle.net/123456789/1362.

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18

Korvorapun, Korkit. "Site-Selectivity in Ruthenium-Catalyzed C–H and C–C Activations." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2020. http://hdl.handle.net/21.11130/00-1735-0000-0005-148C-7.

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19

Liu, Weiping. "Ruthenium- and Manganese-Catalyzed C−O and C−C Formation via C−H Activation." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2016. http://hdl.handle.net/11858/00-1735-0000-0028-8771-3.

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20

Raghuvanshi, Keshav. "Ruthenium(II)-Catalyzed C-N, C-O and C-C Formations by C-H Activation." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2017. http://hdl.handle.net/11858/00-1735-0000-002B-7D4C-2.

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21

Bowen, John George. "C-H activation in the formation of C-N and C-O Bonds." Thesis, University of Bristol, 2015. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.685335.

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The regioselective activation of C-H bonds and subsequent transformation into desirable functional groupS is an attractive prospect in organic synthesis. We have developed two novel C-H functionalisation reactions; the first is an intramolecular, sulfonamide directed, C-H amination reaction for the synthesis of 3_phenylisoindolinone derivates and the second is a sulfonamide directed ortho C-H acetoxylation reaction. Both isoindolinones and phenol derivatives of sulfonamides are important motifs in numerous pharmaceutically relevant compounds. The Cull-catalysed intramolecular C-H amination rea
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22

Ho, Kelvin. "Rapid increase of molecular complexity through C–H and C–C bond activation." Thesis, University of Liverpool, 2014. http://livrepository.liverpool.ac.uk/2006222/.

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The activation of carbon-hydrogen (C–H) and carbon-carbon (C–C) bonds by transition metal catalysts is an attractive strategy to streamline organic synthesis. Herein this manuscript, the two main areas of research are described. Firstly, it was found that a nickel catalyst can promote the insertion of alkynes into the C–C bond of 3-azetidinones and 3-oxetanones to enable quicker access to pyranones and pyridinones in high yields and excellent regioselectivity. Secondly, a rhodium-catalysed pyridine directed C–H bond activation enables the rearrangement of 1,6-heptadienes into bicyclo[2.2.1]hep
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23

Pierre, Cathleen. "Synthèses de molécules polycycliques par arylation C(sp³)-H intramoléculaire catalysée par le palladium." Phd thesis, Université Claude Bernard - Lyon I, 2012. http://tel.archives-ouvertes.fr/tel-00975446.

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La synthèse de produits complexes se doit de prendre en compte de nouvelles méthodes desynthèse plus efficaces, dont la fonctionnalisation de liaisons carbone-hydrogène. Dans cecontexte, la catalyse homogène par les métaux de transition s'est avérée performante, tout encontrôlant la régio- et la chimiosélectivité de la réaction. Les travaux de thèse présentés dansce manuscrit témoignent de l'efficacité de cette stratégie pour la construction rapide decomplexité moléculaire.Dans un premier temps, nous nous sommes intéressés à l'utilisation de précurseurs chlorés, cequi a permis d'étendre signif
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24

Holstein, Philipp. "Enantioselective C(sp3)-H Arylation and Development of a Modular C(sp3)-H Alkenylation." Thesis, Lyon 1, 2014. http://www.theses.fr/2014LYO10286.

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Récemment, l'activation C-H catalysée par des métaux de transition est devenue un outil performant pour construire des liaisons carbone-carbone et carbone hétéroatome à partir de liaisons C-H omniprésentes dans les molécules organiques. Bien que l'activation des liaisons C-H aromatiques ait été largement étudiée ces dernières années, celle des liaisons C-H aliphatiques représente encore un domaine faiblement exploré. Notre équipe s'est depuis plusieurs années intéressée au développement méthodologique de l'activation C(sp3)-H et à son application en synthèse de produits naturels et molécules b
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25

Sun, Zhicheng. "Computational Study of C−H/C−C Activation and Functionalization with Nitrene, Carbene and Related Complexes." Thesis, University of North Texas, 2020. https://digital.library.unt.edu/ark:/67531/metadc1752352/.

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This dissertation involves inorganic/organometallic catalysis models, in particular the functionalization of carbon-hydrogen and carbon-carbon bonds. Computational methods have been utilized to better understand the factors affecting the kinetics and thermodynamics of C−H and C−C bond activation/functionalization in this dissertation. Chapter 2 investigates methane C−H activation with a diiminopyridine nitride/nitridyl complex of 3d transition metals and main group elements via three competing pathways: 1,2-addition/[2 + 2] addition, insertion and H-atom abstraction/proton coupled electron t
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26

Schinkel, Marvin. "Rutheniumkatalysierte Addition von nicht aktivierten C(sp²)–H- und C(sp³)–H-Bindungen an Alkene." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2013. http://hdl.handle.net/11858/00-1735-0000-0015-A380-B.

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27

Roudesly, Fares. "Fonctionnalisation C-H dirigée d'hétérocycles azotés." Thesis, Sorbonne université, 2018. http://www.theses.fr/2018SORUS354.

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Ce travail de thèse a apporté sa contribution et de nouvelles connaissances dans le domaine de l’activation / fonctionnalisation C-H de noyaux azotés de type pyridine et pyrrole. D’abord, nous avons développé une méthode permettant l’allylation et l’oléfination régiosélective d’azines N-oxyde en utilisant un complexe de Pd(0) formé in situ. Le champ d’application de cette réactivité a ensuite été étudié. Des études expérimentales et des calculs DFT nous ont permis de proposer un mécanisme pour les étapes d’allylation et d’isomérisation. Nous proposons que l’étape d’activation C-H est l’étape c
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28

Coxon, Thomas. "Investigating rhodium-catalysed hydroacylation and carbon-carbon bond activation." Thesis, University of Oxford, 2017. https://ora.ox.ac.uk/objects/uuid:26111304-1563-4c18-956e-67636b87983a.

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The work described in this thesis documents the development of new rhodium(I)-catalysed methodologies within two areas of research. The first examines the use of carbonyls as chelating groups in hydroacylation to produce synthetically valuable ketones and enones. The second area explores new carbon-carbon bond activation methodologies. Chapter 1 presents a literature review of the historical development of rhodium-catalysed hydroacylation, with a focus on chelating groups that can currently be used to suppress decarbonylation. A brief review of methodologies that avoid the requirement for a te
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29

Macdonald, Margaret G. Templeton J. L. "Hydrocarbon C-H activation with Tp[prime]Pt complexes." Chapel Hill, N.C. : University of North Carolina at Chapel Hill, 2007. http://dc.lib.unc.edu/u?/etd,788.

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Thesis (Ph. D.)--University of North Carolina at Chapel Hill, 2007.<br>Title from electronic title page (viewed Dec. 18, 2007). " ... in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Chemistry." Discipline: Chemistry; Department/School: Chemistry. On t.p., [prime] is the mathematical symbol.
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30

Boutadla, Youcef. "Acetate-assisted C-H activation : mechanism, scope and applications." Thesis, University of Leicester, 2010. http://hdl.handle.net/2381/8592.

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This thesis describes mechanistic investigations of acetate assisted C-H activation, the synthesis of cyclometallated complexes containing nitrogen donor ligands via this method and the applications of cyclometallated complexes in terms of insertion reactions. Chapter one introduces the synthesis, by C-H activation, of cyclometallated complexes containing C,N bidentate ligands of palladium, ruthenium, rhodium and iridium. The introduction also gives an overview on the mechanisms of C-H activation and the applications of C-H activation in catalysis, particularly in direct arylation. Chapter two
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31

Ravetz, Megan Sarah. "Effect metal electron density on C-H activation reactions." Thesis, University of Salford, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.360458.

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32

Fowles, E. H. "Transition metal multihydrides and aspects of C-H activation." Thesis, University of Leeds, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.233726.

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33

Fan, Cheng. "Dichloroboryls, diboration and C-H activation with platinum complexes." Thesis, University of Bristol, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.443267.

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34

Ren, Xinkun. "A P450 BM3 toolkit for C-H activation synthesis." Thesis, University of Oxford, 2016. https://ora.ox.ac.uk/objects/uuid:1a41b822-3ba6-4116-af79-ad268e382a95.

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Cytochrome P450s are a superfamily of haem-dependent enzymes that catalyse the oxidation of natural organic compounds, most commonly via insertion of an oxygen atom from atmospheric dioxygen into a carbon-hydrogen bond. Since there is widespread interest in the selective functionalisation of C-H bonds, P450s have been extensively studied and evolved, particularly P450BM3 from Bacillus megaterium, which is catalytically self-sufficient. In this thesis, a P450BM3 variant library has been developed based on four 'generic accelerators', which have showed enhanced activity towards a broad range of
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35

Bechtoldt, Alexander. "Aerobic Ruthenium-Catalyzed C–H Activations." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2018. http://hdl.handle.net/11858/00-1735-0000-002E-E492-A.

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36

Palazzolo, Alberto. "Development of new methods for the hydrogen isotope exchange catalyzed by metallic nanoparticles." Thesis, Université Paris-Saclay (ComUE), 2019. http://www.theses.fr/2019SACLS276.

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Les composés marqués aux isotopes de l’hydrogène possèdent des nombreuses applications lors des phases précliniques de développement des médicaments. Par exemple, les composés deutérés sont utilisés comme étalons internes dans la quantification par LC-MS de métabolites alors que les molécules tritiées sont souvent des radiotraceurs de choix dans les études d’absorption, distribution, métabolisme et excrétion (ADME) moléculaire des candidats médicaments. Après une brève introduction, un premier chapitre discutera du développement d’une méthode douce et sélective, catalysée par des nanoparticule
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37

Guo, Xiangyu. "Ruthenium-catalyzed C-C bond formation via functional-group directed C-H bond activation." Thesis, McGill University, 2012. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=110570.

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AbstractRuthenium-Catalyzed C-C Bond Formation via Functional-Group Directed C-H Bond ActivationXiangyu GuoAdvisor: Prof. Chao-Jun LiMcGill UniversityThis thesis is an investigation on the formation of carbon-carbon (C-C) bonds in the presence of ruthenium catalyst.In the first part of this thesis, oxidative dehydrogenative coupling reactions for carbon-carbon (C-C) bond formation are described. A ruthenium-catalyzed dimerization of 2-phenylpyridine derivatives is demonstrated to synthesize biaryls using iron(III) chloride as the terminal oxidant. In addition, the oxidative cross coupling of a
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38

Rogge, Torben. "Experimental and Computational Studies on Ruthenium- and Manganese-Catalyzed C-H and C-C Activation." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2019. http://hdl.handle.net/21.11130/00-1735-0000-0005-1298-B.

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39

Poater, Teixidor Albert. "Isomerism and C-H, C-C, O-O, C-O bond activation studies by transition metals." Doctoral thesis, Universitat de Girona, 2006. http://hdl.handle.net/10803/7939.

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Aquesta tesi és el reflex que de la cooperació entre grups experimentals i grups teòrics s'aconsegueix l'assoliment d'objectius inassolibles de forma individual. A partir de la DFT s'expliquen processos inorgànics i organometàl·lics de gran valor biològic i/o industrial. La tesi està enfocada especialment a l'estudi de complexos mononuclears i binuclears de coure, on té lloc l'activació d'enllaços C-H, C-C, i O-O. L'estudi de complexos octaèdrics de ruteni ha permès dur a terme extensos estudis isomèrics i racionalitzar les propietats espectroscòpiques dels mateixos. A més a més, estudis més p
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40

Thongpaen, Jompol. "Ligands NHCs bifonctionnels en fonctionnalisation C-H métallo-catalysée." Thesis, Rennes, Ecole nationale supérieure de chimie, 2019. https://www.ensc-rennes.fr/formations/doctorats.

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La fonctionnalisation directe des liaisons Carbone-hydrogène (C-H) a pris, au cours des deux dernières décennies, une place de plus en plus importante en synthèse organique. En particulier, la fonctionnalisation CH catalysée par un métal de transition (TM) a connu une amélioration croissante de ses performances, permettant ainsi d'élargir la palette d'outils disponibles pour la synthèse de matériaux organiques, de produits naturels et de principes actifs. Néanmoins, le développement de nouvelles transformations de liaisons C-H fonctionnant efficacement en conditions douces avec une large tolér
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41

Barday, Manuel. "Rapid access to heterocycles using transition-metal catalysed C-H and C-C bond activation." Thesis, University of Liverpool, 2018. http://livrepository.liverpool.ac.uk/3029020/.

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42

Holthausen, Michael H., Tayseer Mahdi, Christoph Schlepphorst, Lindsay J. Hounjet, Jan J. Weigand, and Douglas W. Stephan. "Frustrated Lewis pair-mediated C–O or C–H bond activation of ethers." Royal Society of Chemistry, 2014. https://tud.qucosa.de/id/qucosa%3A35977.

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Protocols for the FLP-mediated transformation of ethers are presented. Distinct reaction pathways involving either C–O or C–H bond activation occur depending on the application of oxophilic B(C6F5)3 or hydridophilic tritylium ions as the Lewis acid.
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43

Pahls, Dale R. "Pathways for C—H Activation and Functionalization by Group 9 Metals." Thesis, University of North Texas, 2015. https://digital.library.unt.edu/ark:/67531/metadc801909/.

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As fossil fuel resources become more and more scarce, attention has been turned to alternative sources of fuels and energy. One promising prospect is the conversion of methane (natural gas) to methanol, which requires an initial activation of a C-H bond and subsequent formation of a C-O bond. The most well studied methodologies for both C-H activation and C-O bond formation involve oxidation of the metal center. Metal complexes with facile access to oxidation states separated by four charge units, required for two subsequent oxidations, are rare. Non-oxidative methods to perform C-H bond activ
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44

Duin, Marcel Adrianus. "Nucleophilic and electrophilic platinum compounds for C-H bond activation." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2004. http://dare.uva.nl/document/75218.

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45

Lopez, Suarez Laura. "Tetra-substituted olefin synthesis using palladium-catalysed C-H activation." Thesis, University of Edinburgh, 2012. http://hdl.handle.net/1842/5869.

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In an effort to obtain more efficient and greener chemical transformations, a substantial amount of research interest has been directed towards the use of arene C-H bonds as functional groups. Hydroarylation of alkynes through direct functionalisation of C-H bonds has been studied in recent years leading to the development of high-yielding metal-mediated processes. The main aim of the current work is the addition of a third component in the hydroarylation of alkynes trough C-H activation, in order to achieve a second C-C bond formation. Attempts at palladium-catalysed three-component reaction
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46

Liu, Xin-Zhu. "Development of late transition metal catalysed direct C-H activation." Thesis, Imperial College London, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.530451.

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47

Black, Stephen Ian. "Synthetic and mechanistic studies related to C-H bond activation." Thesis, Imperial College London, 1988. http://hdl.handle.net/10044/1/46966.

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48

Crosby, Sarah H. "Cyclometallated complexes of platinum : C-H activation, oxidation and reduction." Thesis, University of Warwick, 2011. http://wrap.warwick.ac.uk/55449/.

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Within this thesis, research related to the synthesis of Pt(II) and Pt(IV) cyclometallated complexes involving both aryl and alkyl C-H activation is discussed. The introduction reviews literature relevant to C-H activation, cyclometallation and reductive elimination, both historic and current. Four pyridine based pro-ligands, all with a 4-fluorophenyl substituent and a varying alkyl substituent, were synthesised in order to study both aryl and alkyl C-H activation. Initial reactions with K2PtCl4 led to the cyclometallation of the phenyl ring via a reversible aryl C-H activation, which then res
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Lackner, Sebastian. "Nickel-Catalyzed Secondary Alkylations and Fluoroalkylations via C–H Activation." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2016. http://hdl.handle.net/11858/00-1735-0000-0028-87C8-1.

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50

Dupont, Jairton. "Activation-fonctionnalisation intramoleculaire de liaisons c-h par le palladium." Université Louis Pasteur (Strasbourg) (1971-2008), 1988. http://www.theses.fr/1988STR13197.

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