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Dissertations / Theses on the topic 'Metalation'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Timmons, Michael. "Directed Ortho-Metalation of Dimethylarylamines." TopSCHOLAR®, 2002. http://digitalcommons.wku.edu/theses/641.

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Site-specific product(s) from the reaction of benzene derivatives with various reagents is a need of researchers at numerous laboratories, particularly those in the pharmaceutical industry. Such derivatives can be synthesized directly, i.e., by substitution of a proton, using either of two procedures: electrophilic aromatic substitution (EAS) or directed ortho-metalation (DoM). Directed ortho-metalation (DoM) is an alternative aromatic substitution process initiated by organolithium reagents which provides regiospecific substitution exclusively at the ortho- position (equation). The focus of t

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2

Campbell, Smith Alison May. "Controlling directed metalation in aromatic systems." Thesis, University of Cambridge, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.610077.

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3

Shelton, Phillip. "Metalation of the Di- and Tri-Methoxybenzenes." TopSCHOLAR®, 2001. http://digitalcommons.wku.edu/theses/701.

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Hydrocarbon solvents are known to be unreactive towards organolithium reagents and also to afford little support for ortho-metalation reactions. In contrast, both m- and odimethoxybenzene afford 80% "ion-multiple specific" monometalation in hydrocarbon solvent (n-hexane, cyclohexane, toluene) without the addition of any catalyst (ether or amine). These observations are, in part, attributed to the 1,2- and 1,3- formation of the n-BuLi dimer, the most reactive form of n-BuLi. In other words these substrates are acting in a "substrate-catalyzed" manner. Extensions of these concepts to 1,2,3-, 1,2

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4

Cai, Xiongwei. "Regiospecific synthesis of alkylphenanthrenes using a combined directed ortho metalation, DoM, (Suzuki-Miyaura cross coupling), directed remote metalation, DreM, methodology." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp05/MQ63276.pdf.

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5

Woosley, Barry. "Directed ortho Metalation in Hydrocarbon Solvents: Opposing Pi-Resonance Effects." TopSCHOLAR®, 2004. http://digitalcommons.wku.edu/theses/539.

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Hydrocarbon solvents are known to be unreactive toward organolithium reagents and do not typically support ortho-metalation reactions without the aid of a promoter. An exception would be an arene substrate having the capability to bidentate complex to the reactive alkyllithium dimer, which enables ortho-metalation to occur in high yields. A second, more limiting exception, would be that the arene substrate possesses localized lone pairs of electrons, as is the case when the directed ortho metalating group (DMG) is located in the benzyl position. The work reported here centers upon developing a

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6

Friesen, Carl. "Directed Ortho-Metalation of the Three Methyl Anisoles in Various Media." TopSCHOLAR®, 1996. http://digitalcommons.wku.edu/theses/870.

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Directed ortho-metalation (DoM) is a very useful alternative to electrophillic aromatic substitution (EAS) for the synthesis of substituted aromatic compounds. DoM is highly regiospecific providing metalation chiefly in the ortho-position. However, lateral (a-) metalation of an alkyl side-chain and ortho-metalation of a second ortho-position can compete. Investigation of the three methylanisoles was therefore undertaken to determine the interplay between these factors and to discover metalation conditions to achieve selectivity. This goal was uniquely achieved for p-methylanisole where conditi

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7

Milburn, Claire Louise Maud Jackson. "The directed ortho metalation reaction of aryl O-carbamates on solid support." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp05/MQ63340.pdf.

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8

Panighel, Mirco. "Adsorption, metalation and magnetic properties of tetra phenyl porphyrins on metal surfaces." Doctoral thesis, Università degli studi di Trieste, 2015. http://hdl.handle.net/10077/10898.

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2013/2014<br>Traditional semiconductor technology will reach a size limit within the next few years. A possible solution could be the use of organic molecules in technological applications as single functional units in metal-organic based devices; the success of this approach strongly depends on the understanding of the behaviour of these molecules on metallic surfaces. The interaction with metallic substrates and the interaction between the molecules themselves determine the electronic and magnetic properties of the system, and it is thus of fundamental interest to study these metal-organic i

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9

Macklin, Todd Kristopher. "The development of sulfamates as latent directed metalation groups. Total synthesis of schumanniophytine. Divergent synthesis of substituted chromone 3- and 8-carboxamides." Thesis, Kingston, Ont. : [s.n.], 2007. http://hdl.handle.net/1974/925.

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10

Fässler, Roger. "The metalation of terminal alkynes by Zn" and their addition to nitrones and aldehydes /." Zürich : [s.n.], 2003. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=14936.

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11

Sousa, Alexandre Carreira da Cruz. "5,10,15,20-meso-tetrapiridilporfirina de európio: síntese, caracterização e investigações espectroscópicas." reponame:Repositório Institucional da UFC, 2015. http://www.repositorio.ufc.br/handle/riufc/20074.

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SOUSA, Alexandre Carreira da Cruz. 5,10,15,20-meso-tetrapiridilporfirina de európio: síntese, caracterização e investigações espectroscópicas. 2015. 62. Dissertação (Mestrado em química)- Universidade Federal do Ceará, Fortaleza-CE, 2015.<br>Submitted by Elineudson Ribeiro (elineudsonr@gmail.com) on 2016-10-04T14:55:21Z No. of bitstreams: 1 2015_dis_accsousa.pdf: 1629715 bytes, checksum: 264276171b2e35ae1514203c752b6856 (MD5)<br>Approved for entry into archive by Jairo Viana (jairo@ufc.br) on 2016-10-10T19:42:17Z (GMT) No. of bitstreams: 1 2015_dis_accsousa.pdf: 1629715 bytes, checksum: 264276

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12

Zegke, Markus. "Reductive metalation of the uranyl oxo-groups with main Group-, d- and f-block metals." Thesis, University of Edinburgh, 2015. http://hdl.handle.net/1842/16186.

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This thesis describes the reductive functionalisation of the uranyl(VI) dication by metalation of the uranyl oxo-groups (O=UVI=O), using reductants from Group I, Group II, Group IV, Group XII and Group XIII as well as from the lanthanide and actinide series of the periodic table. Chapter 1 introduces uranium and nuclear waste, and gives an introduction into uranium(V) chemistry. It further compares the chemistry of uranyl(V) to neptunyl(V), with a specific focus on solid state interactions. The chemistry of the Pacman calixpyrroles is briefly introduced. These macrocyclic ligands form the basi

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13

Kendall, Christopher Nicholas Owen. "The directed ortho metalation - Suzuki-Miyaura cross-coupling connection, towards the total synthesis of dehydrorabelomycin." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape3/PQDD_0020/MQ54462.pdf.

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14

Metallinos, Constantinos. "Development of new directed metalation groups for the (-)-sparteine-mediated synthesis of ferrocenes with planar chirality." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp05/NQ63438.pdf.

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15

Lai, Ping-Shan. "Directed ortho metalation-boronation Suzuki-Miyaura cross coupling leading to synthesis of azafluorenol core liquid crystals." Thesis, Kingston, Ont. : [s.n.], 2007. http://hdl.handle.net/1974/511.

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16

Miller, Ricarda [Verfasser]. "Directed remote Metalation Strategy : Synthesis, Cytotoxicity and DNA-Intercalation of Arnottin I and Schumanniophytine Derivatives / Ricarda Miller." Konstanz : Bibliothek der Universität Konstanz, 2011. http://d-nb.info/1049892801/34.

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17

Sousa, Alexandre Carreira da Cruz. "5,10,15,20-meso-tetrapiridilporphyrin europium: synthesis, characterization ans spectroscopic investigations." Universidade Federal do CearÃ, 2015. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=14722.

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Conselho Nacional de Desenvolvimento CientÃfico e TecnolÃgico<br>Increasingly, porphyrins have gained a position of detached interest in scientific circles. Its high biological compatibility, being a molecule found naturally in plants and many red blood animals, coupled with the possibility of forming complexes with lanthanide atoms, makes these compounds are particularly attractive in a branch of medicine quite promising in terms respect to combat cancer, called photodynamic therapy. The lanthanide-porphyrin complex act as photosensitizers in the production of singlet oxygen, a cytotoxic spec

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18

Kachel, Stefan Renato [Verfasser], and J. Michael [Akademischer Betreuer] Gottfried. "Investigations of Metal/Organic Interfaces and Metalation Reactions of Organic Semiconductors / Stefan Renato Kachel ; Betreuer: J. Michael Gottfried." Marburg : Philipps-Universität Marburg, 2020. http://d-nb.info/1224046862/34.

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19

Rohbogner, Christoph. "TMP2Mg•2LiCl and Related Bases for the Metalation of Unsaturated Substrates and the Role of the Phosphorodiamidate Directing Group." Diss., lmu, 2010. http://nbn-resolving.de/urn:nbn:de:bvb:19-114575.

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20

Chauder, Brian Andrew. "Combined directed ortho metalation-transition metal catalyzed coupling reactions for the synthesis of chromenes, ergot alkaloids, and biaryl macrocycles." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/NQ63410.pdf.

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21

Onuska, Nicholas Paul Ralph. "Studies Towards the Synthesis of 2,5-Disubstituted-3-Fluorothiophenes Using a Directed Ortho-Metalation/Nickel-Catalyzed Cross-Coupling Approach." Kent State University Honors College / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=ksuhonors1460652408.

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22

Balkenhohl, Moritz [Verfasser], and Paul [Akademischer Betreuer] Knochel. "Metalation and amination of N-heterocycles and the halogen/zinc exchange of aryl halides / Moritz Balkenhohl ; Betreuer: Paul Knochel." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2019. http://d-nb.info/1211957128/34.

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23

James, Clint A. "The directed remote metalation-carbamoyl migration reaction, total syntheses of the defucogilvocarcins and Arnottin I and synthesis of heteroarylfused benzopyranones." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp02/NQ32833.pdf.

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24

Green, Anthony Laine. "The Directed ortho Metalation of pyridine derivatives with in situ boronation and links to the Suzuki-Miyaura cross coupling reaction." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/MQ63310.pdf.

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25

Ganiek, Maximilian [Verfasser], and Paul [Akademischer Betreuer] Knochel. "Metalation and Halogen-Lithium exchange of sensitive substrates and mild ester homologation in continuous flow / Maximilian Ganiek ; Betreuer: Paul Knochel." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2018. http://d-nb.info/1172634327/34.

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26

Costa, Wijeendra M. R. S. "Coordination of Chemistry of Re(I) Carbonyl Complexes as Pharmaceutically Important Compounds and Synthesis, Characterization, and Metalation of Novel Phthalocyanine Analogs." University of Akron / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=akron1302492223.

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27

Langgaard, Kristensen Jesper. "Metalation, halogen-metal exchange and Pd(0) catalyzed cross-coupling reactions : application to the synthesis of substituted aromatic and heteroaromatic systems /." [Cph.] : Department of Medicinal Chemistry, Royal Danish School of Pharmacy, 2001. http://www.dfh.dk/phd/defences/previous2002.htm.

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28

Weidmann, Niels [Verfasser], and Paul [Akademischer Betreuer] Knochel. "Preparation of lithium, sodium and potassium organometallics by metalation and halogen/metal exchange in continuous flow / Niels Weidmann ; Betreuer: Paul Knochel." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2020. http://d-nb.info/1220631949/34.

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29

DOMÍNGUEZ, RIVERA MARCOS. "STRUCTURAL AND ELECTRONIC COUPLING OF ORGANIC HETEROAROMATIC MOLECULES ON INORGANIC SURFACES OF OXIDES." Doctoral thesis, Università degli Studi di Trieste, 2017. http://hdl.handle.net/11368/2912861.

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Many novel technologies base their main capabilities on the interface between organic semiconductors and dielectric surfaces. Understanding and manipulating its behaviour becomes then an important task for their development, from production cost to efficiency and better employment qualities. In the present thesis, I dealt the issue of molecular ordering and electronic properties at the organodielectric interfaces of four donor heteroaromatic molecules regarding the rutile-TiO2 (110) surface in an ultra-high vacuum (UHV) environment, combining some of them with a carbon allotrope as acceptor.

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30

Yin, Chunfeng. "Regiospecific synthesis of chlorodihydroxybiphenyls and synthesis of 3,3'-bisaryl substituted BINOLs by combined directed ortho metalation (DoM) and Suzuki-Miyaura cross coupling." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp05/MQ63395.pdf.

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31

Nguyen, Quang. "Reinventing Aromatic Substitution: A Novel Look." TopSCHOLAR®, 2013. http://digitalcommons.wku.edu/theses/1292.

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Electrophilic aromatic substitution (EAS) and directed ortho-metalation (DoM) involve the direct substitution of an arene hydrogen. A major drawback involving EAS is the necessity for harsh forcing conditions for the reaction to proceed. Catalysts such as Lewis acids FeBr3 and AICI3 for the introduction of halogens and acyl groups, respectively, are each highly toxic and corrosive. Textbook preparations of aryl iodides classicaly involved the use of iodine and nitric acid. This approach affords only modest yields and does not provide regiospecific substitution of most substituted aromatics bec

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32

Baldwin, Luke Adam. "Synthesis of Dehydrobenzoannulene-Based Covalent Organic Frameworks." The Ohio State University, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=osu1491561788473597.

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33

Dunst, Cora. "Functionalization of arenes and heteroarenes by metalation with TMP-bases or metal insertion and synthesis of tetrasubstituted alkenyl sulfides via a Cu(I)-mediated carbometalation." Diss., lmu, 2011. http://nbn-resolving.de/urn:nbn:de:bvb:19-141952.

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34

Schwärzer, Kuno [Verfasser], and Paul [Akademischer Betreuer] Knochel. "Highly regioselective addition of organozinc reagents to [1.1.1]propellane and Selective metalation of nitrogen containing heterocycles using 2,2,6,6-tetramethylpiperidyl bases / Kuno Schwärzer ; Betreuer: Paul Knochel." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2021. http://d-nb.info/1232176281/34.

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35

Peel, Andrew James. "Group 11 'ate bases : towards an understanding of solid- and solution-state structures." Thesis, University of Cambridge, 2017. https://www.repository.cam.ac.uk/handle/1810/267910.

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Lithium bis(amido)cuprates are an important class of bimetallic base, which can chemo- and regioselectively metalate aromatic compounds, via directed ortho cupration (DoCu). This thesis begins with an introduction to aspects of the chemistry of organolithium compounds, group 11 organometallic compounds and their lithium 'ate complexes. Examples of such synergic bases are presented and the introduction is concluded with a discussion of lithium bis(amido)cuprate bases, which along with their silver congeners, are the subject of this dissertation. In general, syntheses involve the addition of a l

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36

Michaux, Jérôme. "Méthodologies d'accès à des N-hydroxyphtalimides hautement substitués, vers de nouveaux catalyseurs d'oxydation aérobie." Thesis, Grenoble, 2012. http://www.theses.fr/2012GRENV071/document.

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Dans un contexte industriel où les réactions d'oxydation sont réalisées dans des conditions qui ne satisfont pas toujours les principes de la chimie verte, notre groupe étudie des catalyseurs de structure N-hydroxyphtalimide (NHPI), pour l'oxydation aérobie de substrats organiques variés dans des conditions douces. Dans le but d'obtenir des catalyseurs plus actifs, deux familles d'analogues hautement substitués sur le noyau phtalimide ont été préparées, suivant deux nouvelles méthodologies de synthèse. La première consiste en la bis-ortho-métallation / silylation d'acides ortho-phtaliques non

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37

Dunst, Cora [Verfasser], and Paul [Akademischer Betreuer] Knochel. "Functionalization of arenes and heteroarenes by metalation with TMP-bases or metal insertion and synthesis of tetrasubstituted alkenyl sulfides via a Cu(I)-mediated carbometalation / Cora Dunst. Betreuer: Paul Knochel." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2011. http://d-nb.info/1021307890/34.

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38

Chapell, Brian John. "Development of the di-tert-butylphosphinyl directed metalation group, application to the synthesis of aromatic phosphines, substituted ferrocenes and 7-substituted indoles ; Studies directed towards the total synthesis of biruloquinone." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/NQ60527.pdf.

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39

Haas, Diana [Verfasser], and Paul [Akademischer Betreuer] Knochel. "Metalation and functionalization of 5-membered heterocycles and the tropolone scaffold using TMP-bases and cobalt-catalyzed Negishi cross-coupling reactions of (hetero)arylzinc reagents / Diana Haas ; Betreuer: Paul Knochel." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2016. http://d-nb.info/1137466839/34.

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40

Weber, Alexander. "Supramolecular organisation, conformation and electronic properties of porphyrin molecules on metal substrates." Thesis, University of British Columbia, 2007. http://hdl.handle.net/2429/201.

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The investigation and control of molecular properties is currently a dynamic research field. Here I present molecular level studies of porphyrin molecules adsorbed on metal surfaces via Low Temperature Scanning Tunneling Microscopy/Spectroscopy (STM/STS), supported by complementary X-ray absorption experiments. Intermolecular and molecule-surface interactions of tetrapyrdil porphyrin (TPyP) on Ag(111) and Cu(111) were investigated. TPyP self-assembles on Ag(111) over a wide sample temperature range into large, highly-ordered 2D chiral domains. By contrast, adsorption of TPyP on the more reacti

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41

Andersson, Hans. "Reaction between grignard reagents and heterocyclic N-oxides synthesis of substituted pyridines, piperidines and piperazines /." Doctoral thesis, Umeå : Department of Chemistry, Umeå University, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-25619.

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42

Ziegler, Dorothée [Verfasser], and Paul [Akademischer Betreuer] Knochel. "Metalation and functionalization of pyridones, naphthyridones and pyrones using TMP-bases and Generation of aryl and heteroaryl magnesium reagents in toluene by Br/Mg- and Cl/Mg-exchange / Dorothée Ziegler ; Betreuer: Paul Knochel." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2018. http://d-nb.info/1174142901/34.

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43

Azzouz, Rabah. "Pyridinols protégés et leur utilisation en métallation. Synthèse d'indolizidines à partir de la pyridine : synthèse d'indolizidines à partir de la pyridine." Phd thesis, INSA de Rouen, 2008. http://tel.archives-ouvertes.fr/tel-00559656.

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Dans une première partie, la protection des phénols et des pyridinols a été étudiée. Une nouvelle méthode de tetrahydropyranylation a été développée via la réaction de Mitsunobu. Les pyridinols et des phénols ont ainsi été protégés sous forme d'acétal. Cette méthode est sélective d'un phénol vis-à-vis d'un alcool ou d'une amine. La métallation régiosélective des pyridinols 3- et 4- OTHP a été ensuite réalisée. La fonctionnalisation de ces composés, via des réactions successives de métallation et une hydrolyse acide, a permis la synthèse de pyridinols difonctionnalisés "one-pot". Dans le but d'

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44

Teulade-Fichou, Marie-Paule. "Vers une homologation de la reaction de michaelis-becker : avantage dans la preparation des phosphonates fonctionnels." Paris 6, 1986. http://www.theses.fr/1986PA066599.

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La methode de preparation utilise des carbanions phosphonates lithies (z)::(2)p(y)chrli. Elle realise l'introduction sur le phosphore et le carbone en position 1 de substituants non accessibles par le rearrangement thermique de michaelis-arbuzot. Ce procede est applique a des structures phosphoniques d'interet synthetique et biologique. Ce sont d'une part les alkylidene diphosphonates et d'autre part les formyl-1 phosphonate delta

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45

Zhang, XueYan. "Deprotonative Functionalization of Allylic C(sp³)-H Bonds with N-tert-Butyl-N'-Silyldiazenes." Electronic Thesis or Diss., Sorbonne université, 2025. http://www.theses.fr/2025SORUS009.

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La fonctionnalisation des liaisons C(sp³)-H allyliques revêt une importance majeure en synthèse organique, permettant la construction directe de structures moléculaires complexes sans pré-fonctionnalisation des substrats. Bien que la catalyse par les métaux de transition ait conduit à des avancées significatives dans ce domaine, son coût élevé, la présence de résidus métalliques et les enjeux de durabilité limitent son applicabilité. Cette thèse développe un système sans métal de transition basé sur les N-tert-butyl-N'-silyldiazènes, permettant la fonctionnalisation sélective des liaisons C(sp

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46

Azzouz, Rabah. "Pyridinols protégés et leur utilisation en métallation. Synthèse d'indolizidines à partir de la pyridine : synthèse d'indolizidines à partir de la pyridine." Electronic Thesis or Diss., Rouen, INSA, 2008. http://www.theses.fr/2008ISAM0004.

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Dans une première partie, la protection des phénols et des pyridinols a été étudiée. Une nouvelle méthode de tetrahydropyranylation a été développée via la réaction de Mitsunobu. Les pyridinols et des phénols ont ainsi été protégés sous forme d'acétal. Cette méthode est sélective d'un phénol vis-à-vis d'un alcool ou d'une amine. La métallation régiosélective des pyridinols 3- et 4- OTHP a été ensuite réalisée. La fonctionnalisation de ces composés, via des réactions successives de métallation et une hydrolyse acide, a permis la synthèse de pyridinols difonctionnalisés "one-pot". Dans le but d'

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47

Nickel, Johannes [Verfasser], and Paul [Akademischer Betreuer] Knochel. "Lewis acid triggered regioselective metalation and deprotection of uracils, uridines and cytidines, preparation of pyrrolo[2,3-d]pyrimidines via an intramolecular copper-mediated carbomagnesation of ynamides and regioselective preparation of tetrasubstituted fluorobenzenes / Johannes Nickel ; Betreuer: Paul Knochel." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2016. http://d-nb.info/1142787737/34.

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48

Mosrin, Marc. "Regio- and Chemoselective Metalations of N-Heterocycles." Diss., lmu, 2009. http://nbn-resolving.de/urn:nbn:de:bvb:19-102948.

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49

Thomas, dit Dumont Laurence. "Contribution à la synthèse de la Streptonigrine. Synthèse de 4-phénylpyridines polyfonctionnelles par métallation et couplage croisé." Rouen, 1992. http://www.theses.fr/1992ROUES045.

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Ce travail décrit la synthèse de 4-phénylpyridines polyfonctionnelles nécessaires à la construction du squelette de la Streptonigrine. La stratégie de synthèse de ces dérivés utilise l'association de deux méthodes: la fonctionnalisation par métallation et le couplage biarylique catalysé par le palladium. Ce schéma de synthèse nous a conduit à étudier une méthode d'amination électrophile par voie carbanionique (préparation de 3-aminopyridines diverses), la métallation de pyridine-N-oxydes et le couplage pyridine-benzène. Dans une dernière partie nous avons realisé un couplage phénylpyridine-qui

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Boudet, Nadège. "Polyfunctionalizations of N-Heterocycles via Chemo- and Regioselective Metalations." Diss., lmu, 2008. http://nbn-resolving.de/urn:nbn:de:bvb:19-80314.

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