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Dissertations / Theses on the topic 'Organic azide'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 April 2022

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1

Hartranft, Charles Alan. ""One-pot" synthesis of organic azides from alcohols and protected sugars /." Connect to resource online, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1229370336.

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2

Okumu, Antony A. "Development of a Safe and Efficient Alkyl Azide Synthesis using Arylsulfonyl Azide." Youngstown State University / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1290962115.

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3

Kwarkoh, Angela. "Conversion of Alcohols to Alkyl Azides Using O-Nitrobenzenesulfonyl Azide." Youngstown State University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1380022166.

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4

Dobosh, Brian Joseph. "The Synthesis of Azides from Alcohols using Sulfonyl Azides." Youngstown State University / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1219459733.

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5

Copeland, Christopher N. II. "Modified Conditions for Acyl Azide and Carbamate Synthesis." Youngstown State University / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1473765784542178.

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6

Banerjee, Upasana. "Mechanistic Investigations into the Photoreactivity of Organic Azides in Solution, Crystals and Cryogenic Matrices." University of Cincinnati / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1623250627543686.

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7

Curry, Omadee S. "Reaction of o-Nitrobenzenesulfonyl Azide/n-Butyl Lithium with Hindered Alcohols." Youngstown State University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1379945812.

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8

Zhang, Jianjun. "Library Synthesis of Anticancer and Antibacterial Agents via Azide Chemistry." DigitalCommons@USU, 2010. https://digitalcommons.usu.edu/etd/711.

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Various anticancer and antibacterial agents have been synthesized via azide chemistry by taking advantage of carbohydrate. Starting from the synthesis of 14 glycosyl azides, a library of carbohydrate-oxazolidinone conjugates and a library of carbohydrate-cyclopamine conjugates with biological interests were synthesized based on a highly efficient "click reaction" assisted by sonication. Some of the conjugates have improved solubility and enhanced anticancer activity. A library of neomycin B derivatives with various modifications at the 5" position has been synthesized. Two leads exhibit

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9

Gatlin, DeVonna M. M. S. "Characterization and Photodynamics of Reactive Intermediates for Various Carbonyl-Based Systems: Alkyl Azides, Vinyl Azides, and Beta-Ketoester Moieties." University of Cincinnati / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1535380770508755.

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10

Mandel, Sarah Marie. "Photolysis of Alkyl Azides Containing an Aryl Ketone Chromophore in Solution and the Solid-state." University of Cincinnati / OhioLINK, 2004. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1099539420.

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11

Leopold, Samuel Harris. "Photogeneration of Aryloxenium Ions: Photolysis of 4-acetoxy-4-(4'-methylphenyl)-2,5-cyclohexadienone in Acetonitrile as a Precursor." Miami University Honors Theses / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=muhonors1210088217.

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12

Gill, Joseph B. "Co(II) Based Metalloradical Catalysis| Carbene and Nitrene Transfer Reactions." Thesis, University of South Florida, 2014. http://pqdtopen.proquest.com/#viewpdf?dispub=3666726.

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<p> Radical chemistry has attracted a large amount of research interest over the last few decades and radical reactions have recently been recognized as powerful tools for organic synthesis. The synthetic applications of radicals have been demonstrated in many fields, including in the synthesis of complex natural products. Radical reactions have a number of inherent synthetic advantages over their ionic counterparts. For example, they typically proceed at fast reaction rates under mild and neutral conditions in a broad spectrum of solvents and show significantly greater functional group tolera

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13

Okabayashi, Yohei. "Synthesis of azide- and alkyne-terminated alkane thiols and evaluation of their application in Huisgen 1,3-dipolar cycloaddition ("click") reactions on gold surfaces." Thesis, Department of Physics, Chemistry and Biology, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-20559.

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<p>Immobilization of different bio- and organic molecules on solid supports is fundamental within many areas of science. Sometimes, it is desirable to obtain a directed orientation of the molecule in the immobilized state. In this thesis, the copper (I) catalyzed Huisgen 1,3-dipolar cycloaddition, referred to as a “click chemistry” reaction, was explored as a means to perform directed immobilization of small molecule ligands on gold surfaces. The aim was to synthesize alkyne- and azide-terminated alkanethiols that would form well-organized self assembled monolayers (SAMs) on gold from the comm

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14

LaLama, Matthew. "Rhodium-Catalyzed Decomposition of Carbohydrate Diazo Esters." Youngstown State University / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1532881612843223.

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15

Mayieka, Morgan Ongaga. "Attempted Azidation of Carbohydrate Secondary Alcohols Using Arylsulfonyl Azides." Youngstown State University / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1596709362791187.

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16

Dang, Thao P. "Biomimetic Modeling of the Nitrogen-centered Radical Postulated to occur during the Inhibition of Ribonucleotide Reductases by 2'-Azido-2'-deoxynucleotides." FIU Digital Commons, 2010. http://digitalcommons.fiu.edu/etd/318.

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Ribonucleotide reductases (RNR) are essential enzymes that catalyze the reduction of ribonucleotides to 2'-deoxyribonucleotides, which is a critical step that produces precursors for DNA replication and repair. The inactivation of RNR, logically, would discontinue producing the precursors of the DNA of viral or cancer cells, which then would consequently end the cycle of DNA replication. Among different compounds that were found to be inhibitors of RNR, 2'-azido-2'-deoxynucleotide diphosphates (N3NDPs) have been investigated in depth as potent inhibitors of RNR. Decades of investigation has su

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17

Oakley, Simon Hardie. "Crystallographic determination of wild type, mutant and substrate-analogue inhibited structures of bacterial members of a family of superoxide dismutases : submitted as part of the requirements for the degree of Doctor of Philosophy, Institute of Fundamental Sciences, Chemistry, Massey University, New Zealand." Massey University, 2009. http://hdl.handle.net/10179/1072.

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The iron and manganese superoxide dismutases are a family of metallo-enzymes with highly conserved protein folds, active sites and dimer interfaces. They catalyse the elimination of the cytotoxic free radical superoxide to molecular oxygen and hydrogen peroxide by alternate reduction then oxidation of the activesite with the concomitant transfer of protons from the solvent. There are many key aspects of enzymatic function that lack a structural explanation. The focus of this study is on three crystal structures. The iron-substituted manganese superoxide dismutase from Escherichia coli complexe

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18

Wen, Zhiwei. "Azido- and Triazolyl-modified Nucleoside/tide Analogues: Chemistry, Fluorescent Properties, and Anticancer Activities." FIU Digital Commons, 2018. https://digitalcommons.fiu.edu/etd/3789.

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Two classes of C5 azido-modified pyrimidine nucleosides were synthesized and explored as radiosensitizers. The 5-azidomethyl-2'-deoxyuridine (AmdU) was prepared from thymidine and converted to its cytosine counterpart (AmdC). The 5-(1-azidovinyl) modified 2'-deoxyuridine (AvdU) and 2'-deoxycytidine (AvdC) were prepared employing regioselective Ag-catalyzed hydroazidation of 5-ethynyl pyrimidine substrates with TMSN3. AmdU and AmdC were converted to 5'-triphosphates AmdUTP and AmdCTP, and incorporated into DNA-fragments via polymerase-catalyzed reaction during DNA replication and base excision

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19

Dobosh, Brian J. "The synthesis of azides from alcohols using sulfonyl azides /." Connect to resource online, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1219459733.

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20

Lang, Stuart. "Rearrangement of organic azides." Thesis, University of Strathclyde, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.415093.

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21

Poudel, Dhruba P. "Late-Stage Modification of Polyurethane Dendrimers Using Click Chemistry." Miami University / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=miami1627490978861964.

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22

MacLeod, Fraser. "Novel reactions of organic azides." Thesis, University of Strathclyde, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.501650.

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The intramolecular Schmidt reaction has emerged over recent years as a valuable method for the synthesis of nitrogen-containing molecules. A recent addition to this field has been made within our group consisting of the rearrangement of epoxy azides that has proved extremely useful for the synthesis of pyrrolidines. The scope of this reaction has been further investigated during the studies leading to this thesis. For example, it has been demonstrated for the first time that substrates containing an electron-rich aryl ring can be employed in this aryl amination protocol (Scheme 1). Additionall

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23

Kerbal, Abdelali. "Cycloaddition de diarylnitrilimines et d'azides sur diverses énones et énamines dérivées d'indadones et de tétralones : Regiochimie, diasteréochimie et transformation des cycloadduits." Besançon, 1988. http://www.theses.fr/1988BESA2038.

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La cycloaddition dipolaire-1,3 des diarylnitrilimines sur diverses enones a double-liaison dipolarophile juxtacyclique est regiospecifique. Lorsque le dipolarophile présente deux faces diastereotopiques, l'approche dipole-dipolarographie se fait du côté le moins encombré : - de façon diastereospecifique sur les enones dérivées de l'indanone-1 substituée ou de la tetralone-1 substituée lorsque ces dernières portent en -3 ou -4 un substituant occupant une position axiale - de facon diastereoselective sur les enones dérivées de la tetralone-1 portant un substituant en -4 qui peut adopter une disp

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24

Sagandira, Cloudius Ray. "Exploring acyl azides chemistry in continuous flow systems." Thesis, Nelson Mandela Metropolitan University, 2017. http://hdl.handle.net/10948/12065.

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Organic azides are important in the synthesis of many target molecules of great use in fine chemical and pharmaceutical production. The use of this class of compounds is however limited due to their hazardous nature and many safety concerns, as they are highly exothermic. Micro reactors can handle exotherms extremely well, due to the inherent high surface area to volume ratio, unlike the conventional batch process. This dissertation therefore aims to investigate the safe application of micro reactors in acyl azide chemistry.With this in mind, Chapter 1 provides a comprehensive background on or

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25

Klima, Rodney F. "Triplet Alkyl Nitrene Intermediates: Photolysis of Alkyl Azides with Intermolecular and Intramolecular Triplet Sensitization." Cincinnati, Ohio : University of Cincinnati, 2004. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=ucin1100710601.

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26

Dengiz, Cagatay. "Acyl Azides: Application To The Synthesis Of Various Heterocycles." Master's thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12613892/index.pdf.

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Pyrazoles, isoindolinones, benzodizepinones and dihydroquinolinones are very important heterocycles for their biological properties. Many pharmaceutical agents include these units as core structures. Reactive molecules such as acyl azides, free radicals and formyl groups are used as key step reactants in these studies. Regiospesific hydrolysis and esterifications are used to reach target starting materials. Two different methodology are used for critical ring closure steps. Benzodiazepinones, and isoindolinones are obtained by base mediated ring closure reactions whereas thionyl chloride media

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27

Adero, Philip O. "Heterocycle Synthesis via Rhodium (II)-Catalyzed Azido Carbenoid Cyclization." Youngstown State University / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1348595887.

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28

Mojica, Mike. "Investigation of new synthetic reactions: the synthesis of hydrazines via the Aza-Lossen rearrangement, the synthesis of carbamoyl azides from amines, and deprotection reactions using water at elevated temperatures." Diss., Georgia Institute of Technology, 2014. http://hdl.handle.net/1853/51791.

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This thesis explores three rare synthetic routes: the synthesis of hydrazines via the aza-Lossen rearrangement, the synthesis of carbamoyl azides from amines, and deprotection reactions using water at elevated temperatures. The aza-Lossen reaction was found to be ideal at “infinite dilution” conditions and could be performed with both aryl and alkyl example. Carbamoyl azides could be synthesized in high yields from both aryl and alkyl amines. The carbamoyl azide reaction was found to be much more efficient with Cs (+1) present. Lastly, water at elevated temperatures conditions was efficient at

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29

Canbolat, Eylem. "Organocatalytic Resolution Of Racemic Alpha Azido Ketones." Master's thesis, METU, 2012. http://etd.lib.metu.edu.tr/upload/12614602/index.pdf.

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Chiral cyclic alpha azido ketones are very important compounds in organic chemistry. Because, the reduced forms of them are amino alcohols and these amino alcohols are interesting compounds for their biological activities. They have some pharmaceutical activities such as: potassium channel open up properties, treatment of central nervous system, antihypertensive properties, the agent of dopamin receptor activator, hypolipemic agent and dopamine agonist. These types of compounds have highly acidic alpha-protons, and many kinds of reactions can be performed with them. In this study, mainly, sel

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30

Levita, Giacomo. "Some spectroscopic studies related to atmospheric chemistry and the thermal decomposition of organic azides." Thesis, University of Southampton, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.418998.

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31

Kyei-Baffour, Kwaku. ""One-pot" Synthesis of Carbamates via Curtius Rearrangement." Youngstown State University / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1409143879.

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32

Baboo, Sabyasachi. "Nuclear translation." Thesis, University of Oxford, 2012. http://ora.ox.ac.uk/objects/uuid:5266f049-d576-44fd-ab26-11cf7a27f678.

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In bacteria, protein synthesis can occur tightly coupled to transcription. In eukaryotes, it is believed that translation occurs solely in the cytoplasm; I test whether some occurs in nuclei and find: (1) L-azidohomoalanine (Aha) – a methionine analogue (detected by microscopy after attaching a fluorescent tag using ‘click’ chemistry) – is incorporated within 5 s into nuclei in a process sensitive to the translation inhibitor, anisomycin. (2) Puromycin – another inhibitor that end-labels nascent peptides (detected by immuno-fluorescence) – is similarly incorporated in a manner sensitive to a t

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33

Whipp, Christopher J. "Part 1: The Direct Arylation of Azine N-Oxides with Aryl Triflates Part 2: The Site-Selective Direct Arylation of Substituted Indoles." Thesis, University of Ottawa (Canada), 2010. http://hdl.handle.net/10393/28792.

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Part 1: The Direct Arylation of Azine N -Oxides with Aryl Triflates. Two sets of conditions for the palladium-catalyzed direct arylation of azine N-oxides with aryl triflates have been developed. Using palladium(II) acetate, a trialkylphosphine ligand, a carbonate base and pivalic acid, both mono- and diarylated azine N-oxides could be synthesized in good to excellent yields.* The reaction regioselectivity was examined for 3-substituted pyridine N-oxides, with arylation at C2 being favoured. The methodology was applied to the efficient formal synthesis of a biologically active diaryl pyridin

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34

Shields, Dylan J. "Photochemistry of Organic Azides, Quinones, and Peroxides in Solution, Crystals, Super Molecular Complexes and Cryogenic Matrices." University of Cincinnati / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin157441745178423.

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35

Abdelaziz, Nayera. "Metal-Free and Metal-Based Photochemical Sensitization of Organic Azides in Solution, Crystals, and Cryogenic Matrices." University of Cincinnati / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1624917700560401.

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36

Lopes, Luciana dos Santos. "EFEITO DE UMA AZIDA ORGÂNICA SOBRE A ATIVIDADE DA NTPDase EM LINFÓCITOS HUMANOS." Universidade Franciscana, 2009. http://tede.universidadefranciscana.edu.br:8080/handle/UFN-BDTD/237.

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Made available in DSpace on 2018-06-27T18:56:35Z (GMT). No. of bitstreams: 2 Luciana dos Santos Lopes.pdf: 903442 bytes, checksum: 9241c2c46a0d205e6d9e1b049687e5f7 (MD5) Luciana dos Santos Lopes.pdf.jpg: 3030 bytes, checksum: 0c80e97bb571acad00dbccdd7ce7c921 (MD5) Previous issue date: 2009-01-19<br>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior<br>The NTPDase (apirase-ect, ect-difosfoidrolase, CD39, EC 3.6.1.5) hydrolyses tri nucleotides and/or diphosphate. It is an ectonucleotidase, identified as the antigen surface of lymphoid cells, whose greatest expression leads to an incre

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37

Asor, Angela. "Attempted One Pot Synthesis of Carbamates of Carboxylic Acids via Curtius Rearrangement." Youngstown State University / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1597093471732878.

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38

Bencivenni, Giorgio <1978&gt. "Synthetic and mechanistic investigation of new radical processes: reaction of organic azides with group-XIII Lewis acids." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2008. http://amsdottorato.unibo.it/1052/.

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Dichloroindium hydride revealed to be a valid alternative to tributyltin hydride for radical reduction of organic (alkyl, aryl, acyl, solfonyl) azides. The new approach entails mild reaction conditions and provides high yields of the corresponding amines and amides, also showing high degrees of selectivity. The system dichloroindium hydride / azides can be utilised in fivemembered ring closures of g-azidonitriles, as a new source of aminyl radicals for the attractive synthesis of interesting amidine compounds in the absence of both toxic reagents and tedious purification procedures. Ally

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39

Thenna, Hewa Kosala R. S. "Applications Focused Synthetic Modification on Photoremovable Protecting Groups (PRPG) & Photochemical Analysis on Organic Azides and Isoxazoles." University of Cincinnati / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1511858669354976.

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40

Bisol, Tula Beck. "Preparação e reatividade de um y-azido-ß-hidroxiéster derivado do (E)-4-fenil-3- butenoato de metila." Florianópolis, SC, 2006. http://repositorio.ufsc.br/xmlui/handle/123456789/88500.

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Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Ciências Físicas e Matemáticas. Programa de Pós-Graduação em Química.<br>Made available in DSpace on 2012-10-22T09:49:12Z (GMT). No. of bitstreams: 0<br>Este trabalho apresenta estudos envolvendo síntese e reatividade do (E)-4-fenil-3-butenoato de metila (37) e do derivado anti-4-azido-4-fenil-3-hidroxibutanoato de metila (44) visando a obtenção de heterociclos nitrogenados. Foram realizadas tentativas de preparação do (2-fenil-1-azirin-3-il)acetato de metila (38) e do trans-(3-fenil-1-tosil-aziridin-2-il)acetato de met

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41

Hartdegen, Vera [Verfasser], and Thomas M. [Akademischer Betreuer] Klapötke. "Energetic polymers and plasticizers based on organic azides, nitro groups and tetrazoles : synthesis and characterization / Vera Hartdegen. Betreuer: Thomas M. Klapötke." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2016. http://d-nb.info/1105374033/34.

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42

Vilionskienė, Ingrida. "Krūvius transportuojančių, stabilios amorfinės būsenos hidrazonų, azinų bei antrachinono darinių sintezė ir savybės." Doctoral thesis, Lithuanian Academic Libraries Network (LABT), 2005. http://vddb.library.lt/obj/LT-eLABa-0001:E.02~2005~D_20050726_104916-89724.

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The aims of the work were as follows: • synthesis of branched dimers with stable amorphous state possessing tiophenylsulphide, sulphide and hydroxygroups in the linking fragment of chromophores from aromatic and heteroaromatic alde6 hyde phenylhydrazones. A thorough study of physical and optoelectrographic properties of these charge-transporting compounds; • synthesis of new crosslinkable charge transporting molecular glasses exhibiting high charge carrier mobilities, high morphological stability; • design and synthesis of new hole transporting molecular glasses and polymers (from 9-(2,3-epoxy

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43

Sriyarathne, H. Dushanee M. "Mechanistic Study on Photogeneration of Nitrogen Based Reactive Intermediates via Transient Spectroscopy & Infrared Matrix Isolation Study on Organometallic Reactions with Ozone Forming Metal Oxides." University of Cincinnati / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1504802160622286.

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44

Mudgal, Mukesh M. Dr. "Insight Into the Inhibition of Ribonucleotide Reductases by 2'-chloro-2'-deoxynucleotides and 2'-azido-2'-deoxynucleotides: Biomimetic Studies with Model Substrates." FIU Digital Commons, 2016. http://digitalcommons.fiu.edu/etd/2597.

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Ribonucleotide Reductases (RNRs) are crucial enzymes that catalyze reduction of ribonucleotides to deoxyribonucleotides, required for the biosynthesis of DNA. Vital role played by RNR in the biosynthesis of DNA and its control on cell growth made it one of the main targets for anticancer therapy. Several laboratories clarified the aspects of reaction cascades at active site of RNR. Biochemical studies of RNR by Stubbe for the inactivation of RDPR by 2'-chloro-2'-deoxyuridine-5'-diphosphate emphasizes departure of chlorine as an anion, while biomimetic studies by Robins with 6'-O-nitro-2'-chlor

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45

Davenport, Eric Parker. "Fluorescent Probes to Investigate Homologous Recombination Dynamics." DigitalCommons@USU, 2016. https://digitalcommons.usu.edu/etd/5007.

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There are multiple mechanisms by which DNA can become damaged. Such damage must be repaired for the cell to avoid ill-health consequences. Homologous recombination (HR) is a means of repairing one specific type of damage, a double-strand break (DSB). This complex pathway includes the Rad51-DNA nucleoprotein filament as its primary machinery. Current methodology for studying HR proteins includes the use of fluorescently labeled DNA to probe for HR dynamics. This technique limits the number of proteins that can be involved in experimentation, and often only works as an end reporter. The work her

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46

Zhurakovskyi, Oleksandr. "Pericyclic and related rearrangements for the synthesis of nitrogen heterocyclic ring systems." Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:d7e4bbea-4009-4e7e-838c-46b4bb81bc13.

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The thesis describes synthesis and reactions of allene azides tethered to various functional groups and the application of the discovered cascade transformations towards the synthesis of radianspene J model system. Chapter 1 covers reactions of simple allene azides containing alkyl and cycloalkyl substituents. Thermal rearrangements of these substrates delivered isocyanides and azadienes via the proposed azatrimethylenemethane (ATMM) intermediates. On the other hand, vinylidenecyclopropanes (VDCPs) gave dramatically different products, as described in Chapter 2. A phenyl-substituted VDCP was t

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47

Ananthoji, Ramakanth. "Hydrophilic Polymers of Poly (2-Hydroxy Ethyl Methacrylate) with Tunable Properties for Drug Release, Sequestration of Blistering Agent, Preparation of Ultra-Strong Hydrogels & Thermal Stability of Various Organic Azides." Scholar Commons, 2012. http://scholarcommons.usf.edu/etd/3949.

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The design and synthesis of new finely tunable porous materials has spurred interest in developing novel uses in a variety of systems. Zeolites, inorganic materials with high thermal and mechanical stability, in particular, have been widely examined for use in applications such as catalysis, ion exchange and separation. A relatively new class of inorganic-organic hybrid materials known as metal-organic frameworks (MOFs) has recently surfaced, and many have exhibited their efficiency in potential applications such as ion exchange and drug delivery. A more recent development is the design and sy

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48

Delost, Michael D. "Synthesis of Amine Derivatives from a “One-Pot” Synthesis of Biphenyl-4-methylazide." Youngstown State University / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1442407733.

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49

Heckler, James E. "Advances in gold-carbon bond formation: mono-, di-, and triaurated organometallics." Case Western Reserve University School of Graduate Studies / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=case1441363597.

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50

Boukhris, Abdallah. "Étude par diffraction des rayons X des porphyrines de gallium, germanium et indium, synthons potentiels de conducteurs électriques unidimensionnels." Nancy 1, 1986. http://www.theses.fr/1986NAN10038.

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Étude des composés GA(OEP)(SO::(3)CH::(3)), GA(OEP)N::(3), GE(TPMEPP)(N::(3))::(2), GE(OEP)F::(2) et (OEP) IN-MN(CO)::(5). Caractérisation des groupements azido dans les porphyrines de gallium et de germanium. Première liaison simple métat-métal dans la série des métalloporphyrines. Dopage de fluoro-octaethylporphyrines de gallium et d'octaméthylporphyrines de nickel par l'iode moléculaire. Incommensurabilité des réseaux iode et porphyrine, caractère polymérique des métalloporphyrines. Étude de la conductivité électrique

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