Rozprawy doktorskie na temat „Pyrrole”
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Scott, Mark Simon. "Pyrrole carbinols". Thesis, University of Cambridge, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.615301.
Pełny tekst źródłaArmitage, Georgina Kate. "The Zav'yalov pyrrole synthesis revisited : some derivatives of 3-hydroxy- and 3-amino-pyrroles". Thesis, University of Huddersfield, 2017. http://eprints.hud.ac.uk/id/eprint/34175/.
Pełny tekst źródłaWatt, Esther Jane. "Poly(pyrrole) based gas sensors". Thesis, Birkbeck (University of London), 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.338770.
Pełny tekst źródłaOussaid, Boualem. "Thiophène, pyrrole : synthèse, conformation, macrocycles". Toulouse 3, 1992. http://www.theses.fr/1992TOU30198.
Pełny tekst źródłaOlivier, Andrew John. "Novel carbene complexes with pyrrole ligands". Diss., Pretoria : [s.n, 2001. http://upetd.up.ac.za/thesis/available/etd-02242006-125303/.
Pełny tekst źródłaLaw, Ho. "Synthèse et étude conformationnelle d'hétérocycles soufrés radioprotecteurs : mécanisme réactionnel de formation du cycle thiazolidine : obtention de pyrrole N-éthanethiols". Université Joseph Fourier (Grenoble), 1992. http://www.theses.fr/1992GRE18003.
Pełny tekst źródłaEkinci, Olcun. "Immobilization Of Glucose Oxidase And Polyphenol Oxidase In Conducting Copolymer Of Pyrrole Functionalized Polystyrene With Pyrrole". Master's thesis, METU, 2006. http://etd.lib.metu.edu.tr/upload/2/12607373/index.pdf.
Pełny tekst źródłaVmax and Km. Behavior of enzyme electrodes upon temperature and pH changes were investigated. Glucose oxidase electrode was used for the determination of glucose in orange juice and polyphenol oxidase electrode was used for the determination of polyphenolic compounds in red wine.
Addie, Matthew Stuart. "Synthetic strategies towards pyrrole marine alkaloids". Thesis, University of East Anglia, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.267273.
Pełny tekst źródłaMillan, Barrios Enrique Jose. "Synthesis and electrochemistry of pyrrole derivatives". Thesis, University of Southampton, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.242418.
Pełny tekst źródła鍾惠玲 i Chung Wai-ling Margaret Chiu. "The synthesis and reactions of 3, 5-diaryl-2, 2-bis(ethoxycarbonyl)-2H-pyrroles". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1986. http://hub.hku.hk/bib/B31230829.
Pełny tekst źródłaNgwerume, Simbarashe. "Gold-multifaceted catalysis approach to pyrrole synthesis". Thesis, University of Nottingham, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.604293.
Pełny tekst źródłaMarketwala, Nishrin Ismailbhai. "PYRROLE CARBOXAMIDES AS POTENTIAL CARBONIC ANHYDRASE INHIBITORS". Wright State University / OhioLINK, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=wright1166468773.
Pełny tekst źródłaMirebeau, Jean-Hugues. "Synthèse et réactivité de nouveaux complexes pyrrolylrhénium carbonylés". Paris 6, 2009. http://www.theses.fr/2009PA066083.
Pełny tekst źródłaValderrey, Berciano Virginia. "Calix[4]pyrrole and porphyrin-based molecular assemblies". Doctoral thesis, Universitat Rovira i Virgili, 2013. http://hdl.handle.net/10803/284092.
Pełny tekst źródłaThis thesis is focused on the study of molecular assemblies based on calix[4]pyrroles and porphyrins. The topology and the binding properties of a homoditopic biscalix[4]pyrrole macrotricycle are used to develop three general strategies for the quantitative self-assembly of pseudorotaxane-like complexes. In one strategy, the polyatomic anion of an ion pair is recognized by the supramolecular complex that results when a neutral linear molecule threads the homoditopic macrotricycle. Additionally, the formation of highly stable complexes of ion-pair dimers and quartets of ions by the bis-calix[4]pyrrole receptor through a highly cooperative process is described. Nickel metallated porphyrin tweezers containing calix[4]pyrrole spacers are used in the recognition of the tetrabutylammonium salt of the [6,6]-phenyl-C61-butyric carboxylic acid. Finally, the quantitative self-assembly of a macrocycle formed by the interaction between a rhodium bisporphyrin and a bispyridyl ligand is described. This macrocycle was used in the formation of complexes with [2]pseudorotaxane and [2]rotaxane-like topologies.
Galán, Coca Albano. "Molecular containers based on calix[4]pyrrole scaffolds". Doctoral thesis, Universitat Rovira i Virgili, 2016. http://hdl.handle.net/10803/365311.
Pełny tekst źródłaEsta tesis comprende la síntesis y el estudio de diferentes contenedores moleculares basados en una estructura macrocíclica de calix[4]pirrol. Los contenedores moleculares poseen cavidades polares funcionalizadas ideales para el reconocimiento de moléculas polares i.e. aniones, N-oxidos… La creación de contenedores con cavidades permanentes (cavitandos) da lugar a la formación de complejos termodinámica y cinéticamente muy estables. Las conformaciones adoptadas en disolución por los complejos así como la geometría en estado sólido se discuten en detalle. También se profundizó en el estudio de contenedores moleculares con estructura auto-ensamblada. Se describe la formación de complejos de co-encapsulación ordenados de cloruro y una molécula neutra en el interior de capsulas moleculares basadas en unidades de calixpirol. En un gran esfuerzo sintético, se preparó un contenedor molecular con topología de bis[2]catenano consistente en dos hemisferios de calixpirrol y calixareno unidos mecánicamente. La cavidad anisótropa permitió la co-encapsulación de N-oxidos pequeños con una molécula de disolvente. La gran estabilidad cinética de los complejos formados permitió la estabilización de un N-oxido inestable. La estabilidad termodinámica del complejo supramolecular se relacionó con la cinética de descomposición del N-oxido observado mediante modelos cinéticos. Finalmente, se estudia la síntesis y propiedades de contenedores moleculares con estructura covalente. La preparación de carcerandos formados por la unión (Hay coupling) de dos unidades de tetra-alquinil calixpirrol dio lugar a la formación inesperada de tetrámeros con estructura análoga a un nudo de ocho. El ensamblaje de capsulas covalentes dinámicas que contengan enlaces reversibles de tipo imina también se estudió usando un tetra-formil calixpirrol como esqueleto. En ambos casos se observó que el papel de una molécula plantilla que preorganice el sistema es fundamental para la síntesis eficiente de los contenedores.
This thesis comprises the synthesis and study of different molecular containers based on calix[4]pyrrole scaffolds. The molecular containers possess polar functionalized cavities ideal for the recognition of anions or N-oxides. The preparation of containers with enforced cavities (cavitands) results in the formation of highly stable (both thermodynamic and kinetically) complexes. The conformations adopted in solution by the host and the solid-state geometry are discussed in detail. Furthermore, we also explore the host-guest chemistry of self-assembled molecular containers. We describe the formation of ordered co-encapsulation complexes of chloride with neutral guests within self-assembled hydrogen-bonded molecular capsules having a calix[4]pyrrole core. In a great synthetic effort, a bis[2]catenane molecular container was prepared by the mechanical link of a calixpyrrole and a calixarene hemisphere. The anisotropic cavity of the bis[2]catenane allowed for the co-encapsulation of small N-oxides along with a solvent molecule. The high kinetic stability of the host-guest complexes allowed for the stabilization of a reactive propargylic N-oxide. The observed kinetic stability was related to the thermodynamics of the host-guest complex by a kinetic model. Finally, we studied the synthesis and properties of covalent molecular containers. The preparation of carcerand-like compounds by the Hay coupling of a tetra-alkynyl calix[4]pyrrole afforded the unexpected formation of a figure-of-eight-like structure. The assembly of dynamic covalent capsules bearing reversible imine bonds was also explored using a tetra-aldehyde calix[4]pyrrole as scaffold. In both cases, it was found that the role of the template was vital in the efficient synthesis of the containers.
Almaky, Mahdi M. Almahdi. "DNA-templated poly(N-substituted pyrrole)bipyridinium nanowires". Thesis, University of Newcastle upon Tyne, 2013. http://hdl.handle.net/10443/2127.
Pełny tekst źródłaGuyard, Laurent. "Etude et mecanismes de l'oxydation d'oligomeres de pyrrole". Besançon, 1997. http://www.theses.fr/1997BESA2037.
Pełny tekst źródłaVanNess, Brandon G. "Synthetic approach to epibatidine from 1-(phenylsulfonyl)pyrrole". Wright State University / OhioLINK, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=wright1183494979.
Pełny tekst źródła呂幹雄 i Kon-hung Lui. "Complementary approaches to 2,2-disubstituted 1,4-diketones, and the preparation and properties of 3H- and 3H-pyrroles derived from them". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1988. http://hub.hku.hk/bib/B31231299.
Pełny tekst źródłaKiani, Mohammad Saghir. "Structure and properties of pyrrole based electrically conducting polymers". Thesis, University of Reading, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.316074.
Pełny tekst źródłaPadroni, Giacomo. "Expanding the DNA binding repertoire of pyrrole-imidazole polyamids". Thesis, University of Strathclyde, 2018. http://digitool.lib.strath.ac.uk:80/R/?func=dbin-jump-full&object_id=29599.
Pełny tekst źródłaMaaß, Christian. "Exploring Metal-Ligand Interactions of Pyrrole Based Pincer Ligands". Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2013. http://hdl.handle.net/11858/00-1735-0000-0022-5E31-1.
Pełny tekst źródłaMeure, Samuel James School of Chemical Engineering & Industrial Chemistry UNSW. "Development and characterisation of polypyrrole composites". Awarded by:University of New South Wales. School of Chemical Engineering and Industrial Chemistry, 2006. http://handle.unsw.edu.au/1959.4/24341.
Pełny tekst źródłaJackson, Delwin S. "Synthesis and evaluation of peptidyl and non-peptidyl diphenyl phosphonate esters and a mechanistic study of hydroxy pyrrole and 4-nitroanlide substrates with serine proteases". Diss., Georgia Institute of Technology, 1996. http://hdl.handle.net/1853/27142.
Pełny tekst źródłaThamanavat, Kanrakot. "High Pressure Phase Equilibria in the Carbon Dioxide + Pyrrole System". Thesis, Georgia Institute of Technology, 2004. http://hdl.handle.net/1853/4919.
Pełny tekst źródłaYazicioglu, Emre Yusuf. "Transformation Of Cyclohexanone Derivatives To Bicyclic Furan And Pyrrole Derivatives". Master's thesis, METU, 2004. http://etd.lib.metu.edu.tr/upload/12605269/index.pdf.
Pełny tekst źródłaeither as starting materials for drug substances or many other compounds which have fused heterocyclic rings in their structures and pharmacophore for many complex natural products
syntheses of derivatives of these compounds with different substitution patterns, is an exciting challenge for many scientists. Benzofuran and tetrahydroindole derivatives, which are potent bioactive substances, are synthesized from various cyclohexanone derivatives that are allylated by Stork-enamine or Mn(OAc)3 mediated allylation methods. Allylated ketones are later transformed to benzofuran derivatives upon treatment with base or tetrahydroindole derivatives upon treatment with primary amines.
KANT, ANKUR. "DESIGN AND PATTERNING OF POLY-PYRROLE INTERCONNECTS FOR COCHLEAR IMPLANT". University of Cincinnati / OhioLINK, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1147376799.
Pełny tekst źródłaDevasurendra, Amila Manuradha. "Pyrrole-Based Conductive Polymer Composites for Electroanalysis and Chemical Separations". University of Toledo / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1513257195906402.
Pełny tekst źródłaTravert, Nathalie. "Métabolites pyrrole-2-aminoimidazoles marins bioactifs : réactivité et synthèse biomimétique". Paris 11, 2003. http://www.theses.fr/2003PA112120.
Pełny tekst źródłaThe work described in this manuscript is centered on the reactivity of pyrrole-2-aminoimidazole alcaloids isolated from marine sponges. This study is based on a biogenetic hypothesis which could explain the chemical pathways formation of most of this compounds, starting from very simple precursors like oroidine and dispacamide A. This family of compounds comprise linear and polycyclic structural groups. 2-Pyrrolecarboxylic acid, more or less brominated, and 2-aminoimidazole parts are the most important building blocks. The manuscript is divided into three studies: the study of N1-C and C3-C intramolecular cyclisations on pyrrole-aminoacids derivates allowed us to postulate a new synthetic scheme towards many polycyclic compounds belonging to this family. The study of dimeric pyrrole-proline or proline-proline systems and their biomimetic spontaneous transformations to dispacamide A and derivates. Biomechanistic analysis and the access to oroidine, hymenidine and clathrodine, using N-acyl-1,2-dihydropyridines. This general study allowed us to understand numbers of chemical mecanisms involved in the reactivity of pyrrole-2-aminoimidazole alcaloids
Berlot, Isabelle. "Synthèse, caractérisation et étude électrochimique de tensioactifs dérivés du pyrrole". Université Joseph Fourier (Grenoble), 1998. http://www.theses.fr/1998GRE10087.
Pełny tekst źródłaCohen, Justin Delgado Grubbs Robert H. Dervan Peter B. "Programming protein patterns on DNA nanostructures with pyrrole-imidazole polyamides /". Diss., Pasadena, Calif. : Caltech, 2009. http://resolver.caltech.edu/CaltechETD:etd-11232008-171327.
Pełny tekst źródłaBérubé, Christian Denis. "Delving into the rare-earth metal chemistry of pyrrole-based ligands: Synthesis and analysis of divalent samarium and ytterbium pyrrolide complexes". Thesis, University of Ottawa (Canada), 2001. http://hdl.handle.net/10393/9097.
Pełny tekst źródłaGarcia, Cruz Alvaro. "Micro et Nano structuration du Poly(pyrrole) sur substrat polymérique : développement d’immunocapteur pour la détection des biomarqueurs du cancer". Thesis, Lyon 1, 2015. http://www.theses.fr/2015LYO10105.
Pełny tekst źródłaNon-conventional lithography techniques have made for the two last decades a huge impact in the engineering sciences. They are now regarded as a main challenge for the development of the devices. The objective of this thesis is to explore new alternative possibilities for designing micro & nano biosensors based on poly(pyrrole) (PPy) high resolution microprinting attended by catalytic polymerization (nanoCP-CCP) on substrates Polymer (poly (terephthalate) ethylene (PETE), cyclic olefin copolymer (COC), polyetheretherketone (PEEK), poly (ethylene 2,6-naphthalate (PEN), and polyamide (PI)). In a first step We have developed various printing techniques (grafting printing, addressed printing and direct printing) and polymerization conditions to modulate the characteristics of PPy micro and nano-structured in order to control the size, shape and Electrical desired properties. We found that the most important parameters that affect the printing process especially at the nanoscale are: a.) The ratio of the concentrations of reagents for the polymerization process which includes the Py-silane, nitrate silver (AgNO3), iron chloride (III) / lithium chloride (FeCl3 / LiCl). b) The physical parameters of the GeSIM machine; the printing pressure, contact level, the inking time stamp of polydimethylsiloxane (PDMS), and printing time. Finally, we got to manufacture PPy nanowires (PPy-NW) 747 ± 12.2 nm wide, 114 ± 8 nm in height and with a separation of 573 ± 13.4 nm between two consecutive PPy-NW. These micro and nano-structured films were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM) and electron-photon spectroscopy induced by X-rays (XPS). In the second part, we have developed a PPy-NW-based immunosensors sensitive to interleukin 8 and 6 biomarkers. For this, different strategies have been adopted to immobilize antibodies specific to these two biomarkers. These immunosensors were characterized by electrochemical impedance spectroscopy method (EIS). The results obtained in relation to the sensitivity and selectivity are very satisfactory with the security detection limits of a few pg / L for both developed immunosensors
Sazama, Graham Thomas. "Late First-Row Transition Metals in Weak Ligand Fields - Correlating High-Spin Electronic Structure and Reactivity". Thesis, Harvard University, 2013. http://dissertations.umi.com/gsas.harvard:11012.
Pełny tekst źródłaChemistry and Chemical Biology
李思明 i Sze-ming Lee. "An investigation into novel synthetic routes for 3h-pyrroles". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1989. http://hub.hku.hk/bib/B31209257.
Pełny tekst źródłaFoloppe, Marie-Paule. "Synthèse et étude physico-chimique de N-(benzoyl) prolines et de pyrrolo (2,1-c) (1,4) benzodiazépines à visée thérapeutique". Caen, 1994. http://www.theses.fr/1994CAEN4057.
Pełny tekst źródłaBerini, Christophe. "Réaction des nitrones avec des pyrroles : accès à des N-hydroxylamines chirales. Applications à la synthèse d'acides alpha aminés". Université Joseph Fourier (Grenoble), 2008. http://www.theses.fr/2008GRE10102.
Pełny tekst źródłaThe chemistry of pyrrole and its derivatives is of great interest due to their abundance in many natural and biologically active compounds. The development of new methods to access to functionalized heterocyclic compounds is therefore a promising area. In this context, we have developed a method, in which pyrroles are added onto nitrones in the presence of hydrogen chloride. According to the experimental procedure, either pyrrolic N benzylhydroxylamines or 2,2’ bispyrrolylalkanes could be selectively and efficiently produced. In order to obtain chiral pyrrolic N benzylhydroxylamines, a stereoselective version of this reaction has been developed. Asymmetric inductions from chiral nitrones allow the access to pyrrolic N hydroxylamines with high levels of diastereoselectivities and good yields. The use of a glyoxylate based cyclic chiral nitrone leads to two enantio‐enriched non natural alpha amino acids, the 2’ and 3’ pyrrolylglycines in 22% and 50% overall yield respectively. Moreover, this method has been successfully applied to the total synthesis of Penmacric Acid, a natural product isolated from the seeds of Pentaclethra macrophylla, a leguminous tree, in 11 steps and 17% overall yield. Finally, the results of several biological assays have been performed. The properties as inhibitory of NorA efflux pump and anti‐angiogenic, as well as the activity on the microtubular cytoskeleton are presented
Molina, Muriel Ricardo. "Calix[4]pyrrole based receptors for the recognition of ion pairs". Doctoral thesis, Universitat Rovira i Virgili, 2021. http://hdl.handle.net/10803/670970.
Pełny tekst źródłaLa presente tesis describe la síntesis y los estudios de formación de complejos de receptor sintéticos supramoleculares. Los receptores están basados en calix[4]pirroles, capaces de interaccionar con especies cargadas así como con especies neutras y polares a través de la formación de enlaces de hidrogeno. Los estudios de formación de complejos se llevaron a cabo en cloroformo a través de experimentos de RMN y por calorimetría (en ingles Isothermal Titration Calorimetry, ITC) y en fase gas mediante el uso de técnicas basadas en ESI-MS. En primer lugar, presentamos la síntesis de un bis(calix[4]pirrol) basado en dos unidades de calix[4]pirrol unidos por dos anillos de triazol como espaciadores. El receptor sintético resultó ser adecuado para el reconocimiento de sales de tetraalquilamonio de cianato y cloruro con altos valores de constantes de afinidad. La geometría del complejo y la cooperatividad del evento eran dependientes del catión usado. También investigamos la formación de complejos pseudorotaxanados asistida por pares iónicos usando un N-óxido como componente lineal. Observamos la formación de dos isómeros diferentes dependiendo de la coordinación del anión y el componente lineal en cada uno de las dos cavidades del receptor. Posteriormente, describimos la síntesis de un receptor con topología de [2]rotaxano obtenido mediante la implantación de dos grupos voluminosos a los extremos del componente lineal previamente enhebrado en el macrocíclo (en inglés stoppering).
This thesis describes the synthesis and binding studies of supramolecular synthetic receptors. The receptors are based on calix[4]pyrrole architectures, able to interact with charged and neutral polar molecules by the establishment of hydrogen bonding interactions. The binding studies were performed in chloroform by means of NMR and ITC experiments and in the gas phase by ESI-MS techniques. We present the synthesis of a two-wall bis(calix[4]pyrrole) receptor based on two calix[4]pyrrole units linked by a triazole spacer. The synthetic receptor was able to bind tetraalkylammonium ion pairs of cyanate and chloride with high binding affinity, displaying different binding geometries and cooperativity depending on the bound cation. We then investigated the formation of [2]-pseudorotaxane complexes assisted by the same ion pairs, using a lineal N-oxide as the axle. We observed the formation of two different isomeric forms of the complexes obtained attending to the binding of the anion and the axle on each of the two different hemispheres of the receptor. We also report the synthesis of the [2]rotaxane receptor obtained by stoppering strategy and briefly discussed the binding properties towards ion-pairs. Finally, we describe the synthesis and binding studies of a strapped calix[4]pyrrole macrocycle decorated with a bis-amide unit as the strap.
Maeda, Rina. "Synthesis and Evaluation of the Pyrrole-Imidazole Polyamides for Cancer Treatment". Doctoral thesis, Kyoto University, 2021. http://hdl.handle.net/2433/263806.
Pełny tekst źródła京都大学
新制・課程博士
博士(総合学術)
甲第23345号
総総博第18号
京都大学大学院総合生存学館総合生存学専攻
(主査)教授 山敷 庸亮, 教授 杉山 弘, 教授 積山 薫
学位規則第4条第1項該当
Doctor of Philosophy
Kyoto University
DGAM
Sasaki, Shunta. "DNA sequence-specific alkylation by pyrrole-imidazole polyamides with indole linkers". 京都大学 (Kyoto University), 2008. http://hdl.handle.net/2433/136909.
Pełny tekst źródłaShaw, Shannon Joanne. "The development of polypyrrole-based biosensors". Thesis, View thesis, 1994. http://handle.uws.edu.au:8081/1959.7/23336.
Pełny tekst źródłaCai, Xuediao. "Synthesis and Characterization of Pyrrole Based Adhesion Promoter Systems on Oxide Substrates". Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2005. http://nbn-resolving.de/urn:nbn:de:swb:14-1109334028224-37122.
Pełny tekst źródłaSandrin, Franco. "Lewis acid catalyzed reactions of 1-benzyl-2, 5-bis (trimethylsiloxy) pyrrole". Thesis, McGill University, 1985. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=66047.
Pełny tekst źródłaDuke, Andrew James. "An investigation of the properties of novel, poly(pyrrole)-based conducting polymers". Thesis, University of Southampton, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243095.
Pełny tekst źródłaEvans, Louise Sarah. "Amido-pyrrole, isophthalamide andcalix[4]arene cleft-type receptors fpr anionic guests". Thesis, University of Southampton, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.444970.
Pełny tekst źródłaMagness, Simon Lee. "Distributions and stable isotope characteristics of maleimides (1-H-pyrrole-2,5-diones)". Thesis, University of Bristol, 2001. http://hdl.handle.net/1983/c048b2c8-5524-4e7d-ac52-d473a31b78fb.
Pełny tekst źródłaCai, Xuediao. "Synthesis and Characterization of Pyrrole Based Adhesion Promoter Systems on Oxide Substrates". Doctoral thesis, Technische Universität Dresden, 2004. https://tud.qucosa.de/id/qucosa%3A24463.
Pełny tekst źródłaDUCHENET, DEPIERRE VIRGINIE. "Monomeres et oligomeres fonctionnalises dans les series du thiophene et du pyrrole". Caen, 1996. http://www.theses.fr/1996CAEN2040.
Pełny tekst źródłaHuang, Hao. "Quinone-Pyrrole Dyad Based Polymers for Organic Batteries : From Design to Application". Doctoral thesis, Uppsala universitet, Nanoteknologi och funktionella material, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-316492.
Pełny tekst źródłaCortés, Sánchez Antonio Emilio. "A synthetic biology approach to the biosynthesis of novel pyrrole-amide antibiotics". Thesis, University of Strathclyde, 2016. http://digitool.lib.strath.ac.uk:80/R/?func=dbin-jump-full&object_id=28480.
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