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Dissertations / Theses on the topic 'Claisen rearrangement'

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Published: 4 June 2021

Last updated: 25 July 2025

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1

Yoon, Tehshik Peter MacMillan David W. C. "The acyl-Claisen rearrangement development of a novel metal-catalyzed Claisen rearrangement and enantioselective variants of the acyl-Claisen rearrangement /." Diss., Pasadena, Calif. : California Institute of Technology, 2002. http://resolver.caltech.edu/CaltechTHESIS:01282010-153053761.

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Thesis (Ph. D.)--California Institute of Technology, 2002. PQ #3052855.<br>Advisor names found in the Acknowledgments pages of the thesis. Title from home page. Viewed 02/11/2010. Includes bibliographical references.

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2

Mountford, David Mark. "Novel Claisen rearrangement reactions." Thesis, Imperial College London, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.415168.

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3

Yang, Yanbo. "Pd0-Catalyzed Formal 1,3-Diaza-Claisen Rearrangement. Design And Development Of Cationic 1,3-Diaza-Claisen Rearrangement." ScholarWorks @ UVM, 2014. http://scholarworks.uvm.edu/graddis/261.

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The dissertation describes Pd0-catalyzed formal 1,3-diaza-Claisen rearrangement and the design and development of cationic 1,3-diaza-Claisen rearrangement. Our previous work has shown that isocyanates react with azanorbornenes and azabicyclo[2.2.2]octenes under thermal conditions to afford zwitterionic intermediates that undergo a thermal 1,3-diaza-Claisen rearrangement to give both ureas and isoureas. However, some azanorbornenes and azabicyclooctenes failed to rearrange or proceeded in low yields. To address these challenging substrates for the thermal 1,3-diaza-Claisen rearrangement, we hav

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4

O'Brien, Alexander. "Acyclic stereocontrol in the Claisen rearrangement." Thesis, Imperial College London, 2010. http://hdl.handle.net/10044/1/5560.

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This thesis examines the issues of acyclic stereocontrol in the Claisen rearrangement, with particular emphasis on the effects of exopericyclic stereocentres – i.e. those adjacent to the array of atoms directly involved in the sigmatropic process. It is divided into three main parts: The first section provides a review of the field of acyclic stereocontrol. The models used to explain the development of relationships between stereocenters in systems lacking well-defined conformational constraints are discussed. This is an established field and particular emphasis is given to recent developments

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5

Mohamed, Mustafa Abdi. "Synthesis of [alpha]-allynyl and [alpha]-allylsilane amino acids by the Claisen rearrangement /." *McMaster only, 2001.

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6

Voûte, Nicholas. "Rearrangements in the indolo[2,3-b]quinoline system : a novel approach to the synthesis of perophoramidine and the communesins /." Thesis, St Andrews, 2008. http://hdl.handle.net/10023/486.

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7

Garcia-Torres, Jason. "Development of a dual Fries-Claisen rearrangement strategy." Thesis, Loughborough University, 2012. https://dspace.lboro.ac.uk/2134/11002.

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Synthetic approaches towards linear fused carbon rings have been developed over the last decades due to their high interest as compounds with potential antibiotic activity and as organic electronics. The application of a novel iterative route towards linear fused carbon ring systems could provide a versatile new mode of access to complex substituted ring systems. Studies have previously demonstrated the use of an allylation-double Claisen-RCM sequence to build fused carbon rings (C). In this thesis we described our work to expand the use of this methodology by developing milder reaction condit

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8

Neal, Andrew. "Use of the Claisen rearrangement in natural product synthesis." Thesis, University of St Andrews, 2018. http://hdl.handle.net/10023/16129.

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9

Fuhry, Mary Ann Monica. "The Claisen rearrangement route to octalactins A and B." Thesis, University of Cambridge, 1995. https://www.repository.cam.ac.uk/handle/1810/271938.

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10

Barmettler, Peter. "Säurekatalysierte Amino-Claisen-Umlagerungen von 2, 6-Disubstituierten N-Propargylanilinen." [Fribourg, Switzerland] : Institut für Organische Chemie, Universität Freiburg (Schweiz), 1985. http://catalog.hathitrust.org/api/volumes/oclc/21856572.html.

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11

Oxford, Anona June. "Synthesis of unsymmetrically substituted benzenes." Thesis, University of Oxford, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.238182.

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12

Betson, M. S. "A silicon controlled Ireland-Claisen rearrangement as a stereoelectronic probe." Thesis, University of Cambridge, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.596612.

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The work described in this thesis concerns the study of two general types of silicon-controlled Ireland-Claisen rearrangements, 152 and 155. We propose that the transition states for these two rearrangements are sterically very similar, but the flow of electron density is in opposite directions for the two cases. Any significant difference in the diastereoselectivities of the two rearrangements can therefore be ascribed to the difference in electronic nature of the transition states. Our studies showed that both classes of rearrangement gave the <i>anti</i> products with good to excellent sele

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13

NOWACZYK, STEPHANIE. "Thio-rearrangement de claisen asymetrique controle par un groupe alkylsulfinyle." Caen, 2000. http://www.theses.fr/2000CAEN2042.

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Nous avons developpe une nouvelle version asymetrique du thio-rearrangement de claisen et nous avons prouve l'efficacite du groupement alkylsulfinyle en tant qu'auxiliaire de chiralite. Nous avons realise la synthese d'un dithioester et d'un thioamide -cyclohexylsulfinyles enantiopurs. Le diacetone-d-glucose, peu onereux et facilement accessible, a ete utilise comme source de chiralite. Les aminothioacetals de cetene, substrats du rearrangement, sont prepares par une reaction specifique des composes thiocarbonyles, la s-alkylation de l'enethiolate du thioamide enantiopur par des halogenures al

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14

Pham, Thi-Nhan Nguyen. "Thio-rearrangement de claisen : facilite, reversibilite, synthese de composes thiocarbonyles." Caen, 1987. http://www.theses.fr/1987CAEN2045.

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15

Júnior, Paulo Eliandro da Silva. "Estratégias de heterociclização aplicadas a produtos naturais e sintéticos subexplorados pela química medicinal." Universidade de São Paulo, 2014. http://www.teses.usp.br/teses/disponiveis/60/60138/tde-04062014-112413/.

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O presente trabalho divide-se em três capítulos: Capítulo I - Nova síntese de ?-xiloidona: rearranjo de Claisen em hidroxinaftoquinonas; Capítulo II - Síntese e estudo de reatividade de promissores núcleos heteroaromáticos subexplorados pela química medicinal; Capítulo III - Análise computacional de similaridade e propriedades físico-químicas dos núcleos heterocíclicos do capítulo II. O capítulo I descreve uma nova rota para a síntese de ?-xiloidona, um produto natural relacionado ao lapachol, subexplorado pela química medicinal. Esta rota é baseada no rearranjo propargílico de Claisen, a part

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16

Wong, Kong-ching, and 王港政. "Studies on the copper hydride mediated reductive Claisenrearrangement." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2013. http://hub.hku.hk/bib/B50899661.

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17

Tellam, James Peter. "An Ireland-Claisen approach to beta-hydroxy alpha-amino acids." Thesis, University of Bath, 2010. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.541238.

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18

Beaulieu, Patrick. "Approach to the synthesis of spiroiridal-type triterpenoids via an Ireland-Claisen rearrangement." Thesis, University of Ottawa (Canada), 2004. http://hdl.handle.net/10393/26576.

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The formation of carbon-carbon bonds in an asymmetric manner is a central goal of modern synthetic chemistry. Many methods have been developed to form a variety of linkages and substitutions, however the asymmetric formation of quaternary carbons of spirocycles is still a formidable challenge. These compounds represent special challenges because of the requirement of double ring formation together with the control of facial selectivity during the formation of a quaternary carbon centre. The present work demonstrates our efforts towards establishing a strategy based on the Ireland-Claisen rearr

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19

Jamieson, Andrew G. "Investigation of a new substrate directed aza-Claisen rearrangement for natural product synthesis." Thesis, University of Glasgow, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.443415.

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20

Perrio, Stéphane. "Diastereoselectivite du thio-rearrangement de claisen : induction asymetrique par un centre chiral oxygene." Caen, 1991. http://www.theses.fr/1991CAEN2046.

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Le thio-rearrangement de claisen de trois familles d'alpha hydroxydithioacetals de cetene s-allyles a ete etudie. Il conduit a des beta hydroxy-dithioesters alpha allyles a deux ou trois carbones asymetriques contigus. A chaque fois une excellente diastereoselectivite a ete observee: 1) a partir de dithioacetals comportant un carbone prochiral et un carbone asymetrique, on obtient majoritairement au moins a 85% des dithioesters de stereochimie syn; 2) avec des dithioacetals presentant un seul carbone prochiral et deux carbones asymetriques contigus et configuration relative syn, on botient ave

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21

Pollex, Annett. "Viridiofungins and xeniolide F: target oriented synthesis using different rearrangement reactions of a common substrate class." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2006. http://nbn-resolving.de/urn:nbn:de:swb:14-1160474365794-44380.

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The present dissertation covers the total synthesis of viridiofungin triesters and studies toward the total synthesis of xeniolide F. In both cases, sigmatropic rearrangements of α-allyloxy substituted α,β-unsaturated esters are employed: for the viridiofungin ester synthesis a [2,3]-Wittig rearrangement and for the xeniolide F synthesis a catalytic asymmetric Claisen rearrangement CAC. For both rearrangement reactions the historical development, main characteristic and important variations are discussed. The viridiofungin triester synthesis represents a convergent and highly flexible route to

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22

Walker, Joel. "Generation Of Electron Deficient Carbodiimides And Their Application In The Guanidine Forming, Zwitterionic 1,3-Diaza-Claisen Rearrangement." ScholarWorks @ UVM, 2017. http://scholarworks.uvm.edu/graddis/674.

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The 1,3-diaza Claisen rearrangement was initially discovered by the Madalengoitia group in the early 2000s. Tertiary, allylic, amines nucleophilically add to the carbon of a heterocumulene (isocyanate, isothiocyanate, or carbodiimide) to generate a zwitterion which then undergoes [3,3]-sigmatropic rearrangement. The rearrangements conducted with a carbodiimide generate guanidine-containing skeletons. The guanidine functional group is found in many biologically active products, making it a worthwhile chemical target. To this end, strained, tertiary, allylic, amine 2-benzyl-2-azabicyclo[2.2.1]he

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23

Tait, Joanne Margaret. "Water-promoted reactions for organic synthesis : the Claisen rearrangement and the Baylis-Hillman reaction." Thesis, University of Reading, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.250705.

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24

Dong, Vy Maria Dervan Peter B. "Novel variants of the zwitterionic Claisen rearrangement and the total synthesis of erythronolide B /." Diss., Pasadena, Calif. : California Institute of Technology, 2004. http://resolver.caltech.edu/CaltechETD:etd-02252004-175803.

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25

Lewis, Simon Eliot. "The decarboxylative Ireland-Claisen rearrangement : methodology studies and approaches to the total synthesis of (-)-suaveoline." Thesis, Imperial College London, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.429457.

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26

Knott, Jane Marie. "Studies on Pyridine n-oxides." Thesis, University of Oxford, 1995. http://ora.ox.ac.uk/objects/uuid:cc74d06b-9840-4695-9f47-961583da147c.

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The work described herein is directed towards the Claisen rearrangements and [3+2] cycloaddition reaction of pyridine N-oxide systems. The pyridine N-oxide molecule is a very versatile and useful synthetic intermediate for the construction of more complex pyridines. Chapter 1 contains a review of work carried out within the group towards Claisen rearrangement of benzene-type systems. The acid catalysed rearrangement of these systems affords a high degree of regioselectivity. A literature survey of the [3+2] cycloaddition reaction of both aliphatic nitrones and aromatic N-oxides with various di

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27

Defosseux, Magali. "Ouvertures électrophiles de cyclopropylcarbinols : synthèse totale de la zincophorine." Paris 6, 2004. http://www.theses.fr/2004PA066079.

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28

Fuentes, SaÌnchez Daniel. "Ketene-Claisen rearrangement of Î±,Î²-unsaturated heteroacetals and enantioselective synthesis of glycidic amides via sulfur ylides." Thesis, University of Bristol, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.411094.

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29

Harker, Wesley. "A mechanistic insight into the synthesis of enantiopure β-amino acids using the enamido Ireland Claisen rearrangement". Thesis, University of Bath, 2011. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538146.

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30

Ishibashi, Jacob Shotaro Afaga. "BN Isosteres of Acenes for Potential Applications in Optoelectronic Devices." Thesis, Boston College, 2017. http://hdl.handle.net/2345/bc-ir:107613.

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Thesis advisor: Shih-Yuan Liu<br>This dissertation describes progress in the field of polycyclic boron- nitrogen-containing systems, especially for potential application in organic-based optoelectronic devices and hydrogen storage materials. The replacement of a BN unit for a CC unit organic compounds (BN/CC isosterism) can have a profound effect on the electronic structure and even function of a given molecular topology without changing its physical structure very much. Direct comparison between a BN-containing molecule and its direct all-carbon analogue is crucial to establishing the origin

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31

Fairhurst, Nathan W. G. "The Ireland-Claisen rearrangement of 3-alkoxypropenol amino esters as an entry to sphingolipid amino acid natural products." Thesis, University of Bath, 2012. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.571861.

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The Ireland-Claisen rearrangement is a powerful synthetic tool which allows predictable diasterocontrol and chirality transfer in the synthesis of γ,δ-unsaturated carboxylic acids. Previous work within the Carbery group has developed a novel protocol for the synthesis of β-alkoxy- and aryloxy-α-amino acids. Chapter 2 covers the initial volume of work on developing this methodology further to allow the synthesis of sterically congested α-quaternary carbon centres in β-alkyoxy- and aryloxy-α-amino acids. Individual substrate optimisation allowed improvement of both the yields and diastereoselect

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32

Khatri, Hem Raj. "Synthesis of Complex ortho-Allyliodoarenes via Reductive Iodonio-Claisen Rearrangement and Total Synthesis of Antitumor Antibiotic Derhodinosylurdamycin A." University of Toledo / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1431342601.

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33

Ernouf, Guillaume. "Réarrangements sigmatropiques - Synthèse de cyclopropanes fonctionnalisés." Thesis, Paris 6, 2016. http://www.theses.fr/2016PA066719/document.

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Les cyclopropanes sont rencontrés dans de nombreux produits naturels ou synthétiques bioactifs. Les travaux exposés dans ce manuscrit portent sur le développement de réarrangements sigmatropiques [3,3] impliquant des dérivés de cyclopropénylcarbinols pour accéder à des alkylidènecyclopropanes fonctionnalisés, précurseurs de cyclopropanes diversement substitués. Le réarrangement des cyanates de cyclopropénylcarbinyle a permis d'obtenir des dérivés N-acylés d'alkylidène(aminocyclopropanes). Une méthode efficace et stéréosélective, impliquant le réarrangement d'Ireland-Claisen des glycolates et g

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34

Erhard, Thomas. "Totalsynthese von (±)-Codein durch 1,3-dipolare Cycloaddition." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2011. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-69013.

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Die Nitron-Cycloaddition an ein dearomatisiertes Phenol ermöglichte den leichten Aufbau des Phenanthrengerüstes von Codein in der gewünschten Konfiguration. Weitere Schritte führten mit kompletter Diastereoselektivität zu Allopseudocodein und nach Allylverschiebung durch Hydrolyse der Chlorcodide schließlich zu (±)-Codein.

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35

Luedtke, Matthew William. "Expansion Of The Intramolecular Zwitterionic-1,3-Diaza-Claisen Rearrangement Beyond Bridged-Bicyclic Electron-Deficient Isothioureas To Generate Substituted Cyclic Guanidines." ScholarWorks @ UVM, 2019. https://scholarworks.uvm.edu/graddis/1109.

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Guanidines are ubiquitous in nature and have important applications in biological chemistry and industry, presenting themselves in biomacromolecules and organic materials respectively. The zwitterionic-1,3-diaza-Claisen rearrangement has allowed facile access to a variety of highly-substituted, complex guanidines, which would otherwise require a significant amount of time or resources to synthesize. Previously, the intramolecular version of the 1,3-diaza-Claisen rearrangement has been used to generate tricyclic guanidines from bridged, bicyclic electron-deficient isothioureas. Extension of thi

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36

Bellavance, Gabriel. "Part A: Development of a Modular Synthetic Approach to Polycyclic Polyprenylated Acylphlorogluginols: Total Synthesis of Papuaforin A, B, C, Hyperforin and Formal Synthesis of Nemorosone. Part B: Studies Toward the Synthesis of Ginkgolides." Thesis, Université d'Ottawa / University of Ottawa, 2016. http://hdl.handle.net/10393/34630.

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Polycyclic Polyprenylated Acylphloroglucinols (PPAPs) are a vast family of natural products, which includes more than 200 members. They contain a stunningly complex molecular architecture which in most cases includes a bicyclo[3.3.1]nonane core. PPAPs have been of interest to the scientific community for their intricate structure, their powerful aid in treating many ailments and large portfolio of biological activities. More particularly, they have been of synthetic interest since 1999 with the first report of an approach to these complicated cores by Nicolaou. Herein, we present the first tot

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37

DESERT, STEPHANE. "Controle de la stereochimie en serie acyclique a l'aide du rearrangement de claisen de precurseurs sulfures comportant un centre chiral adjacent." Caen, 1992. http://www.theses.fr/1992CAEN2008.

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De nombreux exemples de rearrangement de claisen ont ete realises en serie sulfuree. Les dithioacetals de cetene precurseurs ont ete synthetises selon deux voies: la premiere est la s-allylation d'un enethiolate de dithioester chiral par un halogenure allylique, et la seconde voie est la synthese de dithioesters allyliques par reaction de mitsunobu avec des alcools allyliques chiraux suivie d'une deprotonation et d'une s-methylation. La transposition sigmatropique 3,3 a ete realisee dans des conditions assez douces: temperature ambiante ou chauffage a 101c. Nos resultats confirment que le rear

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38

Nguyen, Hai Phuoc. "Reductive Iodonio-Claisen Rearrangement of Iodothiophene Diacetates withAllylsilanes and Formal Synthesis of Plavix®andStereoselective synthesis of ß-mannopyranosides via anomeric O-alkyation." University of Toledo / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1481314374546209.

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39

Li, Jim Li Jim. "I, the solid and solution phase synthesis of carbohydrates ; II, the application of a tandem claisen rearrangement/intramolecular Diels-Alder reaction in organic synthesis /." Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 2001. http://wwwlib.umi.com/cr/ucsd/fullcit?p3022204.

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40

Grossmann, Adriana [Verfasser], and Thomas [Akademischer Betreuer] Magauer. "Studies toward the total synthesis of salimabromide via dearomatization of 1-Naphthols and investigation of the Claisen Rearrangement of allyl chlorovinyl ethers / Adriana Grossmann ; Betreuer: Thomas Magauer." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2017. http://d-nb.info/1176971409/34.

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41

ESTIEU, GIONNET KARINE. "Applications des methylenecyclopropanes : synthese des 2,3-methanoaminoacides par rearrangement d'aza-claisen et synthese des tetrahydropyridones bicycliques par cycloaddition 1,3-dipolaire nouvelle voie d'acces regioselective aux 2,2-diakylcyclopentanones." Paris 11, 1997. http://www.theses.fr/1997PA112199.

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Cette these comprend trois parties : la premiere partie concerne une nouvelle synthese regioselective d'un intermediaire cle dans la synthese d'un fongicide : le triticonazole. Apres un bref apercu de l'activite biologique de tels fongicides, puis des differentes methodes de synthese de la 2,2-dimethylcyclopentanone publiees, nous avons developpe une nouvelle voie d'acces regioselective aux cyclopentanones ,-dialkylees, faisant intervenir un agrandissement de cycle c#4->c#5. Dans la seconde partie, apres une etude bibliographique des 2,3-methanoaminoacides et de leurs syntheses, nous avons pro

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42

Mullins, Toby. "Dearomatising Claisen rearrangements." Thesis, Imperial College London, 2015. http://hdl.handle.net/10044/1/43802.

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This thesis is divided into four chapters. Chapter one is a review of dearomatising [3,3]-sigmatropic rearrangements and is split by sub-classification of Claisen rearrangements. Chapter two introduces the decarboxylative Claisen rearrangement (dCr) and details investigations of the application of this reaction to compounds containing furan rings. Chapter three focuses on the natural product hinckdentine A. It begins with a brief review of previous studies towards the natural product, before discussing attempts to synthesise this compound by a decarboxylative Claisen rearrangement. Chapter fou

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43

Jebreen, Joseph Shiban. "The attempted formation of quaternary centers via a novel intramolecular para-C-alkylation and the use of the aza-Ireland-Claisen rearrangement in the attempted formation of adjacent stereocenters." Thesis, University of Ottawa (Canada), 2004. http://hdl.handle.net/10393/26666.

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The formation of quaternary centers is a formidable challenge. Once these quaternary centers become part of a spirocyclic system, the project becomes even more challenging. The intramolecular para-C-alkylation has been previously used with success. However, no literature precedence is available for an asymmetric version of this reaction. The attempts in synthesizing molecules similar to 123 by using such methodologies are described herein.* Also described is a second project which involved the effective use of the aza-Ireland-Claisen rearrangement in constructing medium-sized rings. These rin

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44

Yow, Shu Hui. "Claisen rearrangements of heterocycles." Thesis, Imperial College London, 2012. http://hdl.handle.net/10044/1/9491.

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This thesis is divided into five chapters. Chapter 1 is a review of de-aromatisation processes achieved by sigmatropic rearrangement. It covers the two main types of sigmatropic rearrangements, namely [2,3]- and [3,3]-rearrangement. Chapter 2 introduces the decarboxylative Claisen rearrangement (dCr) reaction and the aim to investigate its viability on more elaborate heterocyclic substrates is discussed. Research efforts into the synthesis of 3-sulfonyl-6-alkenyl-1,4-dioxan-2-ones are detailed. Chapter 3 discusses the extension of this methodology towards N-alkylmorpholinones. The first sectio

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45

Joshi, U. M. "Studies on diastereoselective C-C bond formation via thio-claisen rearrangement on push-pull ethylene systems incorporating an arene -chromium complex: part A - triphosgene mediated tandem desulfurization-transesterification of alkyl thionocarbamates." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2000. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2290.

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46

Gore, Sophie. "Transannular Claisen rearrangements of α-sulfonyl lactones". Thesis, Imperial College London, 2009. http://hdl.handle.net/10044/1/7827.

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This thesis is divided into three sections. Section one is a review of transannular pericyclic reactions. It covers the four main types of pericyclic reaction and major contributions in the field to date. Recent applications of these reactions to natural product synthesis are also included. Section two discusses the results of research efforts into transannular Claisen rearrangements of α-sulfonyl lactones. The background to the project is discussed along with initial investigations into the transannular Claisen and decarboxylative Claisen rearrangements (dCr) of the 7-membered ?-tosyl lactone

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47

Hutson, Leslie K. "Synthesis of Benzoxazoles Containing Allyl Crosslinking Sites via Claisen Rearrangements." Wright State University / OhioLINK, 1999. http://rave.ohiolink.edu/etdc/view?acc_num=wright974400715.

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48

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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Dimartino, Gianluca. "Ring expansion routes to cyclic fluoroketones by oxy-Cope and Claisen rearrangements." Thesis, University of Birmingham, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.369156.

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Dlubala, Alain. "Etude de la reactivite de dianions formes par double deprotonation de dithioesters beta-thiosubstitues." Caen, 1987. http://www.theses.fr/1987CAEN2010.

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