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Dissertations / Theses on the topic 'Amino-substituted'

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Published: 5 June 2025

Last updated: 1 August 2025

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1

Mellor, Lisa Catherine. "Studies on #beta#-substituted amino acids." Thesis, University of Oxford, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.357423.

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2

Feier-Iova, Ovidiu Cristian. "Synthesis and reactivity of ferrocenyl substituted bis(amino)gallanes." [S.l. : s.n.], 2008. http://nbn-resolving.de/urn:nbn:de:bsz:16-opus-85879.

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3

Gibson, Mairi. "Organozinc and titanium reagents for synthesis of sila-substituted Î±-amino acids and 2-substituted piperidines." Thesis, University of Glasgow, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.400808.

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4

El, Naggar Ossama. "Approaches to the syntheses of c-substituted-a-amino-c lactones." Thesis, McGill University, 1986. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=65948.

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5

Soboyejo, N. O. "Disperse dyes derived from brominated 1,4-amino- or hydroxy-substituted anthraquinones." Thesis, University of Bradford, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.371497.

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6

Kelly, Clare L. "Synthetic routes to isotopically labelled amino acids and substituted #delta#-lactones." Thesis, University of Bristol, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299591.

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7

Alnoman, Rua Bandar A. "Approaches to the synthesis of chiral and amino-substituted BODIPY dyes." Thesis, University of Newcastle upon Tyne, 2016. http://hdl.handle.net/10443/3278.

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Boron dipyrromethenes (BODIPYs) have attracted considerable attention due to their fluorescence properties, including high fluorescence quantum yields and absorption coefficients, good photochemical stability and narrow absorption and emission bandwidths. Because of these properties, they have found extensive use for in vivo imaging, analyte sensing, photodynamic therapy, solar cells and light harvesting arrays. This thesis is divided in two parts. Part one covers the synthesis of functionalised chiral BODIPYs whilst part two involves investigations into the synthesis and application of aminoB

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8

Treweeke, Nigel R. "Preparation of #alpha#-substituted amino acid derivatives by dynamic kinetic resolution." Thesis, University of Sussex, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.390818.

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9

Junker, Philip [Verfasser]. "Formation and reactions of P-amino substituted Li/Cl phosphinidenoid complexes / Philip Junker." Bonn : Universitäts- und Landesbibliothek Bonn, 2021. http://d-nb.info/123191114X/34.

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10

Nguyen, Thi D. T. "Antilarval substituted phenols, distribution of tricyclic pyrones in mice, and synthesis of unnatural amino acids." Diss., Kansas State University, 2014. http://hdl.handle.net/2097/18199.

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Doctor of Philosophy<br>Department of Chemistry<br>Duy H. Hua<br>Three research projects were carried out and they are described below. The synthesis of substituted phenolic compounds including halogenated di- and trihydroxybenzenes, aminophenols, and substituted di-tert-butylphenols are described. Redox potentials of the synthesized molecules along with various known laccase substrates were measured, and an inverse relationship between the oxidation potential and the efficiency of oxidation by laccase of halogenated hydroxybenzenes and aminophenols is demonstrated. The synthesized substitu

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11

Valenrod, Yevgeny. "Development of solid phase-dynamic kinetic resolution for syntheses of N-substituted [alpha]-amino acids." Diss., Online access via UMI:, 2005.

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12

Lowe, Christopher William George. "An investigation into the design and activity of biocidal agents based upon alkyl-substituted amino acids." Thesis, University of Sunderland, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.290902.

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13

Patil, K. M. "Design, synthesis and evaluation of amino- and guanidino-substituted oligomers and oligonucleotides for better cellular uptake." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2013. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2209.

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14

Cakir, Esen. "Synthesis Of Novel Chiral N,n-dialkyl Substituted 1,4-amino Alcohols And Applications In Asymmetric Transformation Reactions." Master's thesis, METU, 2007. http://etd.lib.metu.edu.tr/upload/12608484/index.pdf.

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Amino alcohols are valuable bioactive substances and frequently used as chiral catalyst in various asymmetric transformation reactions. In the synthetic route, the asymmetric synthesis of novel chiral N,N-dialkyl substituted chiral 1,4-amino alcohols are performed starting with meso-anhydride 38. Quinine-mediated desymmetrization of the anhydride with methanol afforded (2S,3R)-cis-monoester 39 with a high enantiomeric excess (up to 98% ee). Chemoselective amidation of hemiester with various N,N-dialkyl substituted amines resulted in amido esters and they were subjected to LAH reduction to affo

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15

Gunler, Zeynep Inci. "Synthesis Of N-(2-propylphenyl) Substituted Chiral Amino Alcohols And Their Usage In Enantioselective Diethylzinc Addition Reactions." Master's thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12613001/index.pdf.

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Chiral 1,2-amino alcohols were synthesized via newly developed &ldquo<br>intramolecular unsaturation transfer&rdquo<br>using cyclohexanone, propargyl bromide, and various chiral amino alcohols as starting components. These amino alcohols can be potential chiral ligands for many asymmetric transformation reactions. Therefore, their effectiveness as chiral ligands in diethylzinc addition to benzaldehyde and N-diphenylphosphinoyl imines were tested. Various parameters including temperature, solvent, ligand amount etc. were screened for the synthesized chiral ligands. In diethylzinc addition to be

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16

Lu, Yingdong. "The development of metal catalyzed, one-step approaches to alpha-amino acids, pyrroles and alpha-substituted amides." Thesis, McGill University, 2009. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=66774.

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THE DEVELOPMENT OF METAL CATALYZED, ONE-STEP APPROACHES TO α-AMINO ACIDS, PYRROLES AND α-SUBSTITUTED AMIDES The purpose of this research was to develop new, one pot methods to assemble nitrogen-contained biologically relevant products, such as pyrroles, amido acid derivatives, and α-substituted amines/amides. These products are all generated from readily available building blocks, such as imines, acid chlorides, alkynes, and/or carbon monoxide, and often via metal catalysis. Chapter 2 of this thesis describes how α-phenoxyamides can be used in palladium catalyzed carbonylatio

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17

Tse, Heong Wai. "Stereoselective synthesis and pharmacological characterisation of #beta#-substituted #beta#-amino acids as selective metabotropic glutamate receptor antagonists." Thesis, University of Bristol, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.337278.

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18

El, Berjawi Rayane. "Construction and characterizations of new perylenediimide based molecular assemblies derived from nitro or amino bay-substituted derivatives." Thesis, Angers, 2019. http://www.theses.fr/2019ANGE0062.

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Les dérivés de pérylènediimide (PDI) font partie des accepteurs d’électrons les plus performants. Leur squelette rigide liéà un système π aromatique étendu, des propriétés optiques et électroniques remarquables et une bonne stabilité chimique et thermique en font de bons candidats comme matériaux de type-n avec de nombreuses applications, en particulier dans le domaine du photovoltaïque organique. Ce travail étudie la réactivité de dérivés pérylènediimides en position «bay» pour la synthèse et la caractérisation de nouveaux systèmes accepteurs originaux dont certains seront utilisés comme maté

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19

Frost, Aileen Bernadette. "Aziridines and aziridinium intermediates in the asymmetric synthesis of beta-substituted-alpha-amino acids and 1,2,3,4-tetrahydroisoquinolines." Thesis, University of Oxford, 2015. http://ora.ox.ac.uk/objects/uuid:ab3aa702-caab-4d20-9057-028258be5fdb.

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This thesis is concerned with the development of methodology for the regioselective ring-opening of aziridines and aziridinium intermediates and its subsequent application to the asymmetric synthesis of β-substituted-α-amino acids and 1,2,3,4-tetrahydroisoquinolines. Chapter 1 introduces methods for the formation of aziridines and aziridinium ions and focusses on their utility as intermediates in synthesis. Chapter 2 describes studies into the synthesis of aziridines from enantiopure α-hydroxy-β-amino esters and their subsequent conversion to the corresponding β-hydr

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20

Stanfield, Charles Freeman. "Synthesis of alpha-amino aldehydes as kallikrein inhibitors; synthetic methods for preparation of beta-substituted cysteine analogues." Diss., The University of Arizona, 1989. http://hdl.handle.net/10150/184738.

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The first half of this dissertation describes the synthesis and biological activities of a series of amino aldehydes; which were derivatives of the basic amino acids, arginine, lysine and ornithine. The synthesis of the amino aldehydes was complicated by the difficulty of producing an intermediate oxidation state (the aldehyde) in the presence of two other functional groups (the α-amino, and the side chain functionality). The amino aldehydes were of biological interest due to the fact that they were inhibitors of the proteolytic enzymes called kallikreins. The kallikreins are known to be invol

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21

Odabas, Serhat. "Asymmetric Synthesis Of N-aryl Substituted Chiral 1,4-amino Alcohol Derivatives And Applications In Various Asymmetric Transformation Reactions." Master's thesis, METU, 2007. http://etd.lib.metu.edu.tr/upload/12608489/index.pdf.

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The asymmetric synthesis of N-aryl substituted chiral 1,4-aminoalcohols and their applications in asymmetric borane reduction and enantioselective diethylzinc addition to benzaldehyde reactions were performed starting from meso anhydride 51 that is the cycloadduct of cyclopentadiene and maleic anhydride. The desymmetrization of meso-anhydride 51 was achieved by using quinine or quinidine with very high enantiomeric excess value (up to 98% ee) and with high chemicalb yield. The quinine-mediated desymmetrization of meso-anhydride 51 with methanol gave (2S,3R)-(-)-cis-monoester 52. The hemiester

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22

Ouellette, Mélanie. "Gas-phase Ion Chemistry of Hydroxy and Amino-substituted Interstellar Polycyclic Aromatic Hydrocarbons and Protonated Polycyclic Aromatic Hydrocarbons." Thesis, Université d'Ottawa / University of Ottawa, 2014. http://hdl.handle.net/10393/31349.

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The gas-phase ion chemistry of hydroxyl- and amino-substituted polycyclic aromatic hydrocarbons (PAHs) and their protonated counterparts were studied using mass spectrometry. Ions were generated using an electron ionization (EI) source and the unimolecular chemistry of metastable ions was studied by performing mass-analysed ion kinetic energy spectrometry (MIKES) experiments with a magnetic sector tandem mass spectrometer. Collision-induced dissociation (CID) experiments were used in conjunction with MIKES experiments to determine ion structure. The ten molecules studied were: 1-naphthol, 2-na

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23

Gallanti, M. "STEREOSELECTIVE SYNTHESIS OF A-AMINO ACIDS B-SUBSTITUTED WITH A 4,5-DIHYDROISOXAZOLE NUCLEUS AND OF TERTIARY AND QUATERNARY ALLYLSILANES." Doctoral thesis, Università degli Studi di Milano, 2012. http://hdl.handle.net/2434/168366.

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In the section A of the thesis is presented a stereoselective synthesis of b-hydroxy-a -amino acids b-substituted with a 4,5 dihydroisoxazole nucleus through an aldol type reaction between Schollkopf reagent and isoxazolynil aldehydes and ketones. In the section B is presented the preparation of allyl- or crotylsilane in high dr and er via the lithiation-borylation reaction of alkylcarbamates with silaboronates.The synthesis of quaternary allylsilane through a related strategy is also presented.

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24

Ghosh, Baidyanath. "Synthesis and Physicochemical Studies on Co-ordination Compounds of molybdenum, Copper, Iron and Zinc with 2-Amino Substituted Pterins." Thesis, University of North Bengal, 2016. http://ir.nbu.ac.in/handle/123456789/2140.

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25

Jäckel, Christian. "Development of a screening system for the systematic evaluation of the interactions of fluoroalkyl-substituted amino acids in polypeptide environments." [S.l.] : [s.n.], 2006. http://www.diss.fu-berlin.de/2006/562/index.html.

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26

Ndungu, John M. "The design and synthesis of novel beta-substituted amino acids, bicyclic dipeptide mimetics, and their incorporation into cholecystokinin/opioidchimeric peptides." Diss., The University of Arizona, 2004. http://hdl.handle.net/10150/290126.

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Peptide ligands and protein receptors play critical roles in the regulation of nearly every biological system. However, peptides are characteristically highly flexible and thus identifying the basic conformational elements necessary for recognition between a peptide ligand and it's receptor at the molecular level remains a formidable task. Great emphasis in peptide research has thus focused on the determination of the receptor-bound conformation adopted by bioactive peptides by synthesizing constrained analogues of the peptides. Knowledge of the three dimensional interaction between a peptide

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27

Xu, Peng. "Asymmetric Synthesis of Nitrogen Containing Bioactive Compounds via the Utilization of Enantiopure p-Toluenesulfinimines." Diss., Temple University Libraries, 2013. http://cdm16002.contentdm.oclc.org/cdm/ref/collection/p245801coll10/id/216585.

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Chemistry<br>Ph.D.<br>The research objective of this thesis research was to develop new methods for the asymmetric synthesis of amine derivatives using p-toluenesulfinimines. Enantiopure sulfinimines are versatile chiral building blocks for the asymmetric synthesis of alkaloids. Sulfinimines were prepared by the condensation of (S)- or (R)-p-toluenesulfinamide with aldehydes and ketones in good to excellent yields, which were prepared from the commercially available Anderson reagent. The first research project was the development of a new method for the preparation of enantiopure anti-anti- α-

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28

GADDIRAJU, NARENDRA VARMA. "Asymmetric Synthesis of C-1 Substituted Cocaine Analogues Using Sulfinimine (N-Sulfinyl Imine) Chemistry And Vinylaluminum Addition to Sulfinimines (N-Sulfinyl Imines) For The Asymmetric Synthesis Of Alpha-Substituted-Beta-Amino Esters." Diss., Temple University Libraries, 2013. http://cdm16002.contentdm.oclc.org/cdm/ref/collection/p245801coll10/id/225834.

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Chemistry<br>Ph.D.<br>Organic nitrogen containing chiral compounds are widely found in nature, and a number of them exhibit important biological and medicinal properties. The main objective of this research is to develop new methods for the asymmetric synthesis of cocaine analogues having methyl (Me), ethyl (Et), n-propyl (n-Pr), n-pentyl (n-C5H11) and phenyl (Ph) groups at the C-1 bridgehead position. The second project concerned the asymmetric synthesis of anti-α-alkyl substituted beta-amino esters, a new chiral building block, utilizing chiral sulfinimine (N-sulfinyl imine) chemistry. The e

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29

Monzón, Díaz Gabriel Andrés [Verfasser], and Paul [Akademischer Betreuer] Knochel. "Zincation of heterocycles and aryl nonaflates : directed magnesiation of highly substituted anilines and amino-substituted heterocycles ; synthesis of heterobenzylic zinc compounds ; new generation of iminium salts / Gabriel Andrés Monzón Díaz. Betreuer: Paul Knochel." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2012. http://d-nb.info/1025821947/34.

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30

Hu, Zilun. "CONSTRAINED β–PROLINES: I. METHANOPYRROLIDINE β-AMINO ACIDS: SYNTHESIS AND CHARACTERIZATION OF NOVEL C6- SUBSTITUTED ANALOGUES AND PEPTIDE OLIGOMERS II. SYNTHESIS OF 2,2-DISUBSTITUTED PYRROLIDINE-3-CARBOXYLIC ACIDS". Diss., Temple University Libraries, 2015. http://cdm16002.contentdm.oclc.org/cdm/ref/collection/p245801coll10/id/339315.

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Chemistry<br>Ph.D.<br>In the study of structurally restricted cyclic β-amino acids and peptides, methanopyrrolidine-5-carboxylic acids (MetPyr-5-acids), or 5-syn-carboxy-2-azabicyclo[2.1.1] hexanes, and derivatives were investigated. MetPyr-5-acids are a series of highly conformationally constrained β-proline derivatives, which belong to a novel category of β-amino acids utilized as building blocks for the synthesis of β-peptides. These β-peptides lack the backbone hydrogen bonds necessary for folding in the usual manner. Substituents and functional groups in this ring system were envisioned t

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31

Flanigan, David L. "Studies in rhodium catalyzed intramolecular C-H insertion of amino acid derived [alpha]-diazo-[alpha]-(substituted)acetamides and its application to the total synthesis of clasto-lactacystin [beta]-lactone." [Tampa, Fla.] : University of South Florida, 2004. http://purl.fcla.edu/fcla/etd/SFE0000418.

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32

Flanigan, David L. Jr. "Studies in Rhodium Catalyzed Intramolecular C-H Insertion of Amino Acid Derived α-Diazo-α-(substituted)acetamides and its Application to the Total Synthesis of clasto-Lactacystin β-Lactone". Scholar Commons, 2004. https://scholarcommons.usf.edu/etd/1037.

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Lactacystin is a microbial metabolite isolated by Omura that exhibits neurotrophic activity in neuroblastoma cell lines. Lactacystin and especially its β-lactone analog are the first examples of non-polypeptide small molecules capable of specifically inhibiting the 20S proteasome. Various asymmetric total syntheses of lactacystin and its analogs have been reported. The total synthesis of clasto -lactacystin β-lactone is achieved using L-serine methyl ester as the starting material and the sole source of stereochemical induction. The success of this synthesis hinges on two featured transformati

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33

Cheng, Ying. "Part I: the 't-amino effect' in the Vilsmeier formylation of p-substituted tertiary anilines : part II: study of the chemistry of aminochlorocarbenes derived from Vilsmeier reagents by the action of bases." Thesis, University of Sunderland, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297371.

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34

Dinsmore, Andrew. "Synthesis of monochiral alanyl substituted heterocycles capable of binding to neuronal glutamate receptors." Thesis, University of Sussex, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.259710.

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35

Norrish, Andrew Mark. "New methods for the synthesis of complex amino acids and carbohydrates." Thesis, University of Exeter, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341169.

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36

Breeze, Liam J. "Cav1.2 pore structure using the substituted-cysteine accessibility method /." Connect to full text via ProQuest. Limited to UCD Anschutz Medical Campus, 2006.

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Thesis (Ph.D. in Neuroscience) -- University of Colorado at Denver and Health Sciences Center, 2006.<br>Typescript. Includes bibliographical references (leaves 108-118). Free to UCD Anschutz Medical Campus. Online version available via ProQuest Digital Dissertations;

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37

Aquino, Estefania da Costa. "Aplicação de 5-bromo-1,1,1-trifluor-4-metoxipent-3-en-2-ona na síntese de pirróis, pirazóis, pirimidinas e 1,2,3-triazóis." Universidade Federal de Santa Maria, 2015. http://repositorio.ufsm.br/handle/1/4275.

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Conselho Nacional de Desenvolvimento Científico e Tecnológico<br>This thesis reports the synthesis of various series of trifluoromethyl substituted nitrogenated heterocycles, such as pyrroles, pyrazoles, pyrimidines and 1,2,3-triazoles, exploiting the synthetic versatility of 5-bromo-1,1,1-trifluoro-4-methoxypent-3-en-2-one in reactions with nitrogenated nucleophiles. In this way, synthesis of a novel series of 4-amino-3-trifluoromethyl-1H-N-substituted pyrroles was performed through two reaction steps. In the first stage is an addition reaction of primary or secondary amine in the 4-position

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38

Hong, Jyun-Wei, and 洪雋為. "Fluorescence Properties of meta-Amino Substituted Stiff Stilbenes." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/81142964130773490215.

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碩士<br>國立臺灣大學<br>化學研究所<br>104<br>Because of the high efficiency in photoisomerization, stiff stilbene derivatives have been employed as photoswitches and sterically restricted substrates. As a result of efficient photoisomerization, stiff stilbenes are low fluorescent chromophores. Regarding the significant meta-amino effect on fluorescence enhancement of trans stilbene, we are interested in the fluorescence properties of stiff stilbene containing N, N-dimethylamino substituent at the meta positions. In this context, meta-amino stiff stilbenes are investigated. To have a full understanding of p

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39

Chen, Li-Ju, and 陳麗如. "Photophysical Properties of Ruthenium (II) Polypyridyl Complexes with Amino Substituted Bipyridine Ligands." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/38791466852360824520.

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碩士<br>國立臺灣師範大學<br>化學系<br>94<br>Ruthenium(II) polypyridyl complexes with amino substituted bipyridine ligands have been synthesized. Two ligands: 4,4’-diamino-2,2’-bipyridine (4,4’-dabpy) and 5,5’-diamino-2,2’-bipyridine (5,5’-dabpy) and six complexes: Ru(4,4’-dabpy)3, Ru(4,4’-dabpy)2bpy, Ru(4,4’-dabpy)bpy2, Ru(5,5’-dabpy)3, Ru(5,5’-dabpy)2bpy, and Ru(5,5’-dabpy)bpy2 were prepared. The MLCT band of the complexes shifts to the red with increasing number of 4,4’-dabpy ligands. The absorption maxima are 471, 481 and 502 nm for Ru(4,4’-dabpy)bpy2, Ru(4,4’-dabpy)2bpy, and Ru(4,4’-dabpy)3, res

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40

Tou, Ｓio-Lon, and 杜兆麟. "Synthesis and Fluorescence Properties of Amino-Substituted Green Fluorescence Protein Chromophore (GFPc)." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/61849576846779961441.

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碩士<br>國立臺灣大學<br>化學研究所<br>101<br>Abstract Green fluorescence protein is isolated form the jellyfish Aequorea Victoria which is a natural photoluminescence species with a high fluorescence quantum yield (0.79). We will discuss the photophysical properties of the green fluorescence protein chromophore analogue in this thesis. The green fluorescence protein chromophore is the emissive moiety of the green fluorescence protein. The syntheized green fluorescence protein chromophore and most of its analogue are not emissive in solution because the fast non-radioactive isomerization process competed wi

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41

Li, Ding-Li, and 李頂立. "Synthesis and Fluorescence Properties of New Meta-Amino Substituted GFP Chromophore Analogues." Thesis, 2017. http://ndltd.ncl.edu.tw/handle/34aztv.

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碩士<br>國立臺灣大學<br>化學研究所<br>105<br>Meta-Amino substituted green fluorescence protein chromophores (GFPc) such as m-DMABDI displays strong fluorescence in non-polar aprotic solvents (e.q., ϕ_f = 0.46 in n-Hex)as a result of the “meta-amino substituent effect” but undergoes fluorescence quenching in protic solvents due to solvent–solute H-bonding interactions. This type of chromophore has been applied in bioimaging, which showed green fluorescence in the hydrophobic regions of human mammary epithelial cells. However, fluorescent dyes with green emission might be interfered by autofluorescence of th

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42

Su, Wen-Chin, and 蘇文欽. "The investigation on the study for preparation of amino substituted galactosyl phytosphingosine." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/632wdd.

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43

Wang, Hui-Min, and 王惠民. "Electrochromic Polyamides and Polyimides Containing Di(4-tert-butylphenyl)amino-Substituted Triphenylamine Moieties." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/54313123196002015188.

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碩士<br>大同大學<br>化學工程學系(所)<br>96<br>A new triphenylamine-based aromatic diamine monomer, N,N-bis(4-aminophenyl)-N',N'-bis(4-tert-butylphenyl)-1,4-phenylenediamine, was successfully synthesized in four steps starting from bis(4-tert-butylphenyl)amine. The newly synthesized diamine monomer was reacted with various dicarboxylic acids and tetracarboxylic dianhydrides to produce two series of novel electroactive polyamides and polyimides with 4-[bis(4-tert-butylphenyl)amino]triphenylamine units in the backbone. Most of the polymers were readily soluble in polar organic solvents, such as N-methyl-2-pyr

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44

Feier-Iova, Ovidiu Cristian [Verfasser]. "Synthesis and reactivity of ferrocenyl substituted bis(amino)gallanes / von Ovidiu Cristian Feier-Iova." 2008. http://d-nb.info/989821382/34.

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45

HsieH, Tai-ran, та 謝泰然. "Synthetic studies toward 3,4,5-trisubstituted-piperidine and cis-4-substituted-5-amino-δ-lactam". Thesis, 2004. http://ndltd.ncl.edu.tw/handle/86407437083433455480.

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46

Chiu, Yu-Jen, and 邱郁仁. "Formation of Heterocyclic Ring on Amino-substituted Naphthoquinone via Palladium Catalyzed C-H Activation." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/26e7zn.

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碩士<br>國立中興大學<br>化學系所<br>107<br>Abstract In this study, several nitrogen-containing naphthoquinone heterocyclic compounds, 4-6, were prepared from naphthoquinone derivatives 1-3c. The reactions were carried out in an open air system and in the presence of Pd(OAc)2 as the catalyst. Firstly, compound 4 was prepared from 1 with cyclohexylamine and in the yield of about 20%. Its crystal structure is resolved via single crystal X-ray determining methods. Obviously, a cyclization process took place during the reaction. Next, two amination products 2_a and 2_b were produced through the reaction of 2 w

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C, Chaitra, and S. Sharada D. "Palladium Catalyzed Aerobic Oxidative Isocyanide Insertion Leading to 2-Amino Substituted 4(3H)-Quinazolinones." Thesis, 2014. http://raiith.iith.ac.in/100/1/CY12M1008.pdf.

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An efficient one-pot cascade aerobic oxidative palladium-catalyzed multicomponent reaction was developed through isocyanide insertion between less active amide NH and aromatic amine. This approach leads to an efficient synthesis of 2- amino-substituted 4(3H)-quinazolinones.

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Behera, Nababrushna. "Chlora and amino substituted cyclocarbaphosphazenes: reagents for organic transformations and precursors for novel ligands." Thesis, 2008. http://localhost:8080/iit/handle/2074/3674.

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Oleksenko, Yaroslav. "Exploring chemically modified polymers: Synthesis of aryl substituted 2-amino-[1,3,4]-oxadiazole conjugated polyacrylic acid." 2008. http://link.library.utoronto.ca/eir/EIRdetail.cfm?Resources__ID=771997&T=F.

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"Development of Amino acid-Substituted Gemini Surfactant-Based Non-invasive Non-Viral Gene Delivery Systems." Thesis, 2013. http://hdl.handle.net/10388/ETD-2013-08-1189.

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Gemini surfactants are versatile gene delivery agents because of their ability to bind and compact DNA and their low cellular toxicity. The aim of my dissertation work was to develop non-invasive mucosal formulations of novel amino acid-substituted gemini surfactants with the general chemical formula C12H25(CH3)2N+-(CH2)3-N(AA)-(CH2)3-N+(CH3)2-C12H25 (AA= glycine, lysine, glycyl-lysine, lysyl-lysine). These compounds were formulated with a model plasmid DNA, encoding for interferon-γ and green fluorescent protein, in the presence of helper lipid, 1,2 dioleyl-sn-glycero-phosphatidyl-ethanolamin

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