Thèses sur le sujet « Catalytic C-H »
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Leitch, Jamie. « Site selective catalytic C-H functionalisation ». Thesis, University of Bath, 2017. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767559.
Texte intégralReynolds, William. « Sequential processes involving catalytic C-H functionalisation ». Thesis, University of Bath, 2014. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.642028.
Texte intégralPaterson, Andrew. « Selective catalytic C-H functionalisation for drug discovery ». Thesis, University of Bath, 2017. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.720659.
Texte intégralIngner, Fredric. « Preparation of carbazolyne precursors through catalytic C-H functionalization ». Thesis, Uppsala universitet, Organisk kemi, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-307497.
Texte intégralGallardo, Donaire Juan. « Synthesis of phthalides and benzolactones via catalytic C-H functionalization/C-O bond-forming ». Doctoral thesis, Universitat Rovira i Virgili, 2014. http://hdl.handle.net/10803/276960.
Texte intégralThe main objective of this Thesis has been the activation of inert C-H bonds catalytically for the construction of C-O bonds. The fist project developed consisted on the activation of C(sp3)-H bonds for the direct synthesis of phthalides catalyzed by Pd, employing simple benzoic acids as starting materials. Continuing in the same research line, the second project described deals with the utilization of cheaper and easy to handle Cu salts as catalyst for the functionalization of C(sp2)-H bonds towards the formation of C-O bonds for the synthesis of benzolactones. Finally, the last project discovered handles a metal-free C-H functionalization approach for the synthesis of benzolactones by using simple iodoarenes as catalyst, thus
Stateman, Leah Marie. « Catalytic Strategies for Remote C-H Functionalization of Alcohols and Amines ». The Ohio State University, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1587554146078308.
Texte intégralWang, Chang-Sheng. « Selective catalytic C(sp²)–H and C(sp³)–H bond functionalizations for the synthesis of phosphorus and nitrogen containing molecules ». Thesis, Rennes 1, 2018. http://www.theses.fr/2018REN1S106/document.
Texte intégralIn the first chapter, we have developed an efficient approach for the fast modification of arylphosphine oxides using ruthenium(II)-catalyzed C–H bond functionalization with alkenes. Interestingly, we have found that the selectivity of the reaction, namely alkylation versus alkenylation, is depending on the reaction pH. The reduction of the phosphine oxide allows the formation of aryl phosphines bearing a flexible pendent carboxylate. In the second objective, a copper-catalyzed oxidative C(sp3)–H/N–H coupling of NH-heterocycles with affordable (cyclo)alkanes was developed. This protocol involved C(sp3)–N bond formation via a radical pathway generated by a homolytic cleavage of di-tert-butyl peroxide and trapping of the radical(s) by copper catalyst.In a third part, benzylic C(sp3)–H acyloxylation of 2-alkylpyridine, 2-alkylpyrazine and 2-alkylthiazole compounds was achieved using simple aldehydes via a copper-catalyzed tandem reaction, involving oxidative esterification followed by O-atom transfer. Finally, pyridin-2-ylmethyl tosylate derivatives are obtained in high yields from 2-alkylpyridine N-oxides via a [3,3]-sigmatropic rearrangement of the adduct between 2-alkylpridine N-oxides with benzenesolfonyl chlorides. Moreover, alkylnitrones also underwant [3,3]-sigmatropic rearrangement to give α-tosylated ketones after hydrolysis
Gerdes, Gerd. « Catalytic C-H activation of benzene by plantinum(II) : a mechanistic study / ». Zürich, 2004. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=15631.
Texte intégralSankey, Rosalind Fay. « Beyond C-H activation : the preparation of novel heterocycles using catalytic dearomatisation ». Thesis, University of Bristol, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559388.
Texte intégralKhan, Imtiaz. « Enolate-directed catalytic C-H functionalization of 2-aryl-1,3-dicarbonyl compounds ». Thesis, University of Nottingham, 2015. http://eprints.nottingham.ac.uk/30261/.
Texte intégralIhara, Hideki. « Directed Catalytic C-H Functionalization of Organoboronic Acids Utilizing Removable Directing Groups on the Boron Atom ». 京都大学 (Kyoto University), 2014. http://hdl.handle.net/2433/188545.
Texte intégralGarcia, Bosch Isaac. « Managanese and dicopper complexes for bioinspired oxidation reactions : catalytic and mechanistic studies on C-H and C=C oxidations ». Doctoral thesis, Universitat de Girona, 2011. http://hdl.handle.net/10803/78940.
Texte intégralEls enzims són molècules d’elevat pes molecular que catalitzen la majoria de processos metabòlics en els éssers vius. Sovint aquestes proteïnes contenen un o diversos ions metàl•lics de la 1a sèrie de transició en el seu centre actiu (Fe, Cu, Co, Mn, Zn, etc.), essent anomenats metal•loenzims o metal•loproteïnes. D’aquests, els metal•loenzims que activen la molècula d’oxigen i l’utilitzen com a oxidant ressalten per la varietat de reaccions catalitzades i la seva exquisida selectivitat. En aquesta tesi doctoral, desenvolupem complexos de baix pes molecular que puguin mimetitzar estructural i/o funcionalment els centres actius de les oxigenases. En una primera part, es descriu la utilització de complexos assimètrics dinuclears de Cu capaços de dur a terme l'oxidació de fenols i fenolats de manera similar a la proteïna tirosinasa. En una segona part, es descriu l'ús de complexos mononuclears de manganès per a l'oxidació d'alcans i alquens.
Crawford, Andrew. « Catalytic borylation of C-H bonds : a route to photophysically interesting pyrene derivatives ». Thesis, Durham University, 2011. http://etheses.dur.ac.uk/663/.
Texte intégralChappell, Benjamin Graham Neil. « A general catalytic β-C-H carbonylation of aliphatic amines to β-lactams ». Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/274756.
Texte intégralIshibashi, Aoi. « Synthesis and Transformation of Organoboronic Acids Using Boron-Modifying Strategy for Catalytic C-H Functionalization ». Kyoto University, 2017. http://hdl.handle.net/2433/225960.
Texte intégralLi, Yingze. « Development of New Cobalt Pincer Complexes for Catalytic Reduction Reactions ». University of Cincinnati / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1554215914263187.
Texte intégralOlsson, Vilhelm. « Development of New Synthetic Routes to Organoboronates by Catalytic Allylic Substitution and C-H bond Functionalization ». Doctoral thesis, Stockholms universitet, Institutionen för organisk kemi, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-27753.
Texte intégralDantignana, Valeria. « Bioinspired metal-based oxidants : selectivity in catalytic hydroxylation of aliphatic C-H bonds and insight into the reactivity of oxoiron species ». Doctoral thesis, Universitat de Girona, 2020. http://hdl.handle.net/10803/671447.
Texte intégralLa oxidación selectiva de enlaces C-H es una reacción importante ya que permite el desarrollo de nuevas estrategias para la síntesis de productos funcionalizados mediante procesos altamente eficientes. No obstante, debido al carácter inerte del enlace C-H, se necesitan oxidantes muy fuertes. Además, conseguir altas selectividades en estas reacciones es especialmente complicado. En este sentido, la naturaleza se puede utilitzar como fuente de inspiración ya que en los sistemas biológicos este tipo de reacciones son catalizadas con alta eficiencia y selectividad por oxigenasas dependientes de hierro. Así pues, el desarrollo de nuevas metodologías sintéticas se basa en el uso de complejos bioinspirados como catalizadores de oxidación. En esta tesis se estudia en primer lugar el uso de complejos bioinspirados de hierro y manganeso para la hidroxilación de enlaces C-H. Posteriormente se investigan compuestos hierro-oxo de alta valencia para comprender mejor sus propiedades oxidativas y poder diseñar así catalizadores más eficientes
Thu, Hung-yat, et 杜鴻溢. « Catalytic C-H bond functionalization reactions catalyzed by rhodium(III) porphyrin, palladium(II) and platinum(II) acetatecomplexes ». Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2006. http://hub.hku.hk/bib/B38798268.
Texte intégralTorigoe, Takeru. « New Molecular Transformations Based on Iridium-Catalyzed Activation of C(sp3)-H Bonds ». 京都大学 (Kyoto University), 2017. http://hdl.handle.net/2433/225636.
Texte intégralThu, Hung-yat. « Catalytic C-H bond functionalization reactions catalyzed by rhodium(III) porphyrin, palladium(II) and platinum(II) acetate complexes ». View the Table of Contents & ; Abstract, 2006. http://sunzi.lib.hku.hk/hkuto/record/B38027872.
Texte intégralAlam, Rauful. « Catalytic Regio- and Stereoselective Reactions for the Synthesis of Allylic and Homoallylic Compounds ». Doctoral thesis, Stockholms universitet, Institutionen för organisk kemi, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-121757.
Texte intégralRosa, Lourenço de Pina Cardoso Bernardo. « Structure of cationic CNHC,Calkyl nickelacycles and their activity in the catalytic functionalization of the C–H bonds of azoles ». Thesis, Strasbourg, 2018. http://www.theses.fr/2018STRAF033/document.
Texte intégralThis thesis develops the study of nickel(II) complexes bearing N-heterocyclic carbene ligands (NHC) in two axes: the synthesis and characterization of nickelacyclic complexes with a carbon-carbon chelating ligand (CNHC,Calkyl); and their catalytic activity in the construction of carbon-carbon bonds (Csp2–Csp2/Csp3) of 1-chalcogene-azoles by carbon-hydrogen (C–H) bond functionalization. A series of cationic CNHC,Calkyl-Ni(II) metallacyclic acetonitrile adducts was synthetized by the removal of a cyclopentadienyl ligand from parent 18 valence electron half-sandwich nickelacycles. The cationic complexes were determined to exist as rare coordinatively and electronically unsaturated T-shaped 14 valence electron Ni(II) species, in the solid state. Application of these new complexes to the cross-coupling of benzothiazole with iodoarenes proved to be a successful strategy in Csp2–Csp2 bond formation, by the combination of a stabilizing metallacyclic scaffold with labile ligands. The discovery of a half-sandwich Ni(II)-(NHC)-(benzothiazolyl) species, inactive in the arylation of benzothiazole, but active for the cross-coupling of benzothiazole with iodoalkanes shows the first example of benzothiazole Csp2–Csp3 bond construction with a Ni(II)-NHC catalyst
Biafora, Agostino [Verfasser], et Lukas J. [Akademischer Betreuer] Gooßen. « Sustainable Methods for the Catalytic Regioselective Transformation of Aromatic Carboxylic Acids via C-COOH and C-H Bond Cleavage / Agostino Biafora ; Betreuer : Lukas J. Gooßen ». Kaiserslautern : Technische Universität Kaiserslautern, 2017. http://d-nb.info/1140760912/34.
Texte intégralSasaki, Ikuo. « Development of Novel Synthetic Methods of Organosilicon Compounds Utilizing Silicon-Containing Reactive Intermediates ». Kyoto University, 2020. http://hdl.handle.net/2433/253508.
Texte intégralChen, Gong. « Studies on Chemo- and Site-Selective C-H Amination of Aniline and Phenol Derivatives with Dirhodium Catalysts and Catalytic Asymmetric Synthesis of Inherently Chiral Calixarenes ». Doctoral thesis, Kyoto University, 2021. http://hdl.handle.net/2433/263599.
Texte intégralPrat, Casellas Irene. « Bioinspired non-heme iron catalysts for challenging oxidative transformations : mechanistic studies and catalytic applications on selective alkane hydroxylation and alkene cis-dihydroxilation ». Doctoral thesis, Universitat de Girona, 2013. http://hdl.handle.net/10803/117778.
Texte intégralLa funcionalització d'hidrocarburs de manera sostenible i eficaç és un dels principals reptes per la química moderna, degut a que la seva abundància natural els fa una important matèria primera. L'oxidació d'hidrocarburs és una de les reaccions més interessants, ja que la introducció d’un àtom d’oxigen en l’estructura d’un hidrocarburs li confereix funcionalitat química, fa augmentar el seu valor i els converteix en reactius adients per subseqüents transformacions químiques. No obstant això, aquestes reaccions són difícils a causa de la inherent baixa reactivitat dels hidrocarburs. Les metodologies actualment disponibles impliquen la utilització d’espècies altament oxidants i tòxiques, altes temperatures i llargs temps de reacció per tal de superar aquesta manca de reactivitat. Aquestes condicions extremes eviten que la química es pugui dur a terme de manera selectiva, fet essencial per produir productes d’alt valor sintètic. Un avanç important és el desenvolupament de metodologies de reacció suaus que permetin l'oxidació d'enllaços C-H i C=C amb alta regio- i estereoselectivitat. Els sistemes naturals, com ara enzims de ferro, són capaços de realitzar aquesta química. El ferro és l’element metàl•lic més abundant a la terra i és clau per nombrosos processos vitals, a més la seva baixa toxicitat el fa un atractiu material per substituir els elements de segona i tercera seria de transició més cars i tòxics emprats actualment. Un dels principals objectius d’aquesta tesi és dissenyar catalitzadors de ferro que imiten l’estructura i la funció dels enzims naturals per tal de trobar una nova metodologia que permeti l'oxidació selectiva d'enllaços C-H i C=C utilitzant condicions suaus i mediambientalment més benignes que les metodologies tradicionals. A més, l’estudi d’aquests sistemes pot donar informació útil sobre el mecanisme d’oxidació del propi enzim. Els resultats obtinguts en aquesta tesi aclareixen el mecanisme pel qual es duu a terme la hidroxilació de l’enllaç C-H amb retenció de la estereoselectivitat en centres mononuclears de ferro, i evidencien la formació d’una espècie de ferro (V) d’alt estat d’oxidació capaç de catalitzar la cis-dihidroxilació d’alquens. A més a més, es descobreix un catalitzador eficient i selectiu capaç de dur a terme aquesta química en condicions d’escala preparativa
Grimster, Neil Patrick. « New strategies for chemical synthesis : 1) Development of a palladium-catalyzed direct C-H alkenylation of indoles by solvent-controlled regioselective C-H bond functionalisation ; 2) Studies towards the development of a catalytic diastereoselective [3,3] sigmatropic rearrangement at ambient temperature ». Thesis, University of Cambridge, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.612869.
Texte intégralDuchane, Christine Marie. « Synthesis, antimicrobial activity, and catalytic activity of rhodium and iridium piano stool complexes : Teaching an old dog new tricks ». Diss., Virginia Tech, 2019. http://hdl.handle.net/10919/101016.
Texte intégralDoctor of Philosophy
Potukuchi, Harish Kumar [Verfasser], Lutz [Akademischer Betreuer] Ackermann et Dietmar [Akademischer Betreuer] Stalke. « Catalytic syntheses and copper- or ruthenium-catalyzed direct C H bond arylations of (hetero)arenes / Harish Kumar Potukuchi. Gutachter : Lutz Ackermann ; Dietmar Stalke. Betreuer : Lutz Ackermann ». Göttingen : Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2011. http://d-nb.info/1043939148/34.
Texte intégralSun, Ho-Yan. « Studies on the Mechanism of Direct Arylation of Pyridine N oxides : Evidence for the Essential Involvement of Acetate from the Pd(OAc)2 Pre-Catalyst at the C-H Bond Cleaving Step ». Thesis, Université d'Ottawa / University of Ottawa, 2011. http://hdl.handle.net/10393/19760.
Texte intégralDietl, Nicolas Paul Richard [Verfasser], et Helmut [Akademischer Betreuer] Schwarz. « Gaseous Oxo-Clusters as Model Systems for C-H Bond Activation and Oxidation Processes – Towards a Better Understanding of Catalytic Mechanisms / Nicolas Paul Richard Dietl. Betreuer : Helmut Schwarz ». Berlin : Universitätsbibliothek der Technischen Universität Berlin, 2013. http://d-nb.info/1032313269/34.
Texte intégralCoetzee, Jacorien. « Towards new catalytic systems for the formation of methyl methacrylate from methyl propanoate ». Thesis, University of St Andrews, 2011. http://hdl.handle.net/10023/2585.
Texte intégralHaslinger, Stefan [Verfasser], Fritz Elmar [Akademischer Betreuer] Kühn, Ulrich K. [Akademischer Betreuer] Heiz, Richard W. [Akademischer Betreuer] Fischer et Jean-Marie [Akademischer Betreuer] Basset. « Bioinspired Iron N-Heterocyclic Carbene Complexes in C–H Bond Oxidation : Reactivity, Electronic Properties, and Catalytic Activity / Stefan Haslinger. Betreuer : Fritz Elmar Kühn. Gutachter : Ulrich K. Heiz ; Richard W. Fischer ; Fritz Elmar Kühn ; Jean-Marie Basset ». München : Universitätsbibliothek der TU München, 2015. http://d-nb.info/1080299270/34.
Texte intégralZhang, 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.
Texte intégralMoselage, 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.
Texte intégralNekkanti, Yelha Phani Kumar. « Ruthenium(II) biscarboxylate-Catalyzed C(sp2)-H and C(sp3)-H Functionalizations by Chelation Assistance ». Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2016. http://hdl.handle.net/11858/00-1735-0000-002B-7CCA-E.
Texte intégralBarzen, Lars [Verfasser], et Gereon [Akademischer Betreuer] Niedner-Schatteburg. « Metal cluster aggregates of the composition Nbn+/-, Con+/- and [ConPtm]+/- as model systems for catalytic C-H activation and structural determination of selected metal peptide complexes of the molecules aspartame (Asp-PheOMe) and Asp-Phe / Lars Barzen. Betreuer : Gereon Niedner-Schatteburg ». Kaiserslautern : Technische Universität Kaiserslautern, 2013. http://d-nb.info/1036129616/34.
Texte intégralBencivenga, Nicholas Ernest. « Enantioselective nickel catalysis : exploiting activated C-H bonds ». Thesis, Massachusetts Institute of Technology, 2012. http://hdl.handle.net/1721.1/73437.
Texte intégralCataloged from PDF version of thesis.
Includes bibliographical references (p. 26-27).
A method for the nickel-catalyzed cross-coupling between benzoxazole and secondary halides was explored. This method was to make use of the activated C-H bond found in benzoxazole at the 2-position to generate the nucleophilic species in situ. After an extensive survey of parameters no such method could be found. However, it was found that copper(I) salts promoted the coupling of benzoxazole and benzylic bromides in high yield, albeit in a racemic fashion. Additionally a method to cross-couple terminal alkynes with secondary halides employing nickel-catalysis was explored. After surveying a number of alkynylmetal species, generated in situ, alkynyl borates were found to cross-couple with allylic chlorides to furnish product with the best enantioselectivity (enantiomeric excess ca. 70%), however in low yield.
by Nicholas Ernest Bencivenga.
S.M.
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.
Texte intégralKorvorapun, 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.
Texte intégralZhang, Yuyang. « Functionalization of alpha- and beta-Amino C-H Bonds Using Cooperative Catalysis : ». Thesis, Boston College, 2020. http://hdl.handle.net/2345/bc-ir:108932.
Texte intégralCooperative catalysis has been developed for transformations where at least two reactants are activated in situ by acid or base sensitive catalysts to form the reactive species and subsequent bond formation leads to desired product. This thesis focuses on the development of ɑ-amino C-H alkynylation and β-amino C-H deuteration through the use of cooperative catalysts. In the alkynylation reaction, N-alkylamines and trimethylsilyl substituted alkynes were used to synthesize propargylamines by the cooperative actions of Lewis acid catalysts, B(C₆F₅)₃ and copper complex. The reaction between in situ generated iminium ion and copper alkyne complex afforded the product. The method is applicable to the late-stage functionalization of bioactive amine drug molecules and has been shown to tolerate different functional groups on trimethylsilyl-substituted alkynes. In addition, an enantioselective and diastereoselective version of the method was also developed through the use of chiral copper complex. In the second part, selective deuteration of β-amino C-H bonds of various acylic and cyclic alkyl amines will be introduced. B(C₆F₅)₃ and Brønsted base work cooperatively to afford enamine and deuterated ammonium ion as reactive intermediate. Deuteration of enamine at the β-position and hydride reduction at the ɑ-position gave the selectively deuterated products. Acetone-d₆ was the found to be the optimal source of deuterium. This method was able to incorporate deuterium atoms up to 99% and can be applied in a gram scale reaction without compromising the yield or d-incorporation level
Thesis (MS) — Boston College, 2020
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
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.
Texte intégralDa, Cruz Ana Cristina Fernandes. « C-H bonds as functional groups for palladium catalysis ». Thesis, University of Bath, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.586169.
Texte intégralHennessy, Elisabeth Therese. « C-H Amination Catalysis from High-Spin Ferrous Complexes ». Thesis, Harvard University, 2013. http://dissertations.umi.com/gsas.harvard:11186.
Texte intégralChemistry and Chemical Biology
Loup, Joachim. « Selectivity Control in 3d Transition Metal-Catalyzed C–H Activation ». Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2019. http://hdl.handle.net/21.11130/00-1735-0000-0003-C19E-1.
Texte intégralLiu, Po Man. « Ruthenium catalysed C-H functionalisation of heteroaromatics ». Thesis, University of Bath, 2015. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.665404.
Texte intégralMerkert, Christine [Verfasser], et Gereon [Akademischer Betreuer] Niedner-Schatteburg. « Metal cluster aggregates of the composition Fen+/, Con+/-, Nin+/- and [ConMm]+/- (M : Au, Rh and Pt) as model systems for catalytic C-H activation and structural determination of ionic dicarboxylic acids as model system for intramolecular hydrogen bonding / Christine Merkert. Betreuer : Gereon Niedner-Schatteburg ». Kaiserslautern : Technische Universität Kaiserslautern, 2014. http://d-nb.info/1051310377/34.
Texte intégralWang, Anqi. « Cu-Catalyzed Amination of sp3 C-H Bonds ». Digital WPI, 2018. https://digitalcommons.wpi.edu/etd-dissertations/509.
Texte intégralSun, G. A. « A study of catalysis by [RuCl(H)(PPh₃)₃] and [η⁵-C₇H₉)RuCl(PPh₃)₂] ». Thesis, University of Sheffield, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.242370.
Texte intégral