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Articles 91 - 120 of 157
Full-Text Articles in Organic Chemistry
Organic Synthesis For Solving Clinical Conundrums Of Drug Activation And For Facilitating Natural Product Drug Discovery, Elkin Libardo Romero
Organic Synthesis For Solving Clinical Conundrums Of Drug Activation And For Facilitating Natural Product Drug Discovery, Elkin Libardo Romero
Open Access Theses & Dissertations
Organic chemistry is an exploratory world in which chemists translate their knowledge by creating new molecules and explore their biological and physical properties. For the past three years, our research has been focused on organic synThesis and chemical biology to solve challenges in this area. Two major approaches have been faced: First, the chemical synThesis of the active metabolite of antithrombotic prodrug Plavix (clopidogrel). Clopidogrel (CPG) has been widely used as an antithrombotic prodrug, which undergoes extensive metabolism in patients; among it, only a trivial portion is converted through a series of cytochrome P450 (CYP)-catalyzed thiophene degradation to form active …
Theranostic Nanoparticles Folic Acid-Carbon Dots-Drug(S) For Cancer, Godwin Kweku Babanyinah
Theranostic Nanoparticles Folic Acid-Carbon Dots-Drug(S) For Cancer, Godwin Kweku Babanyinah
Electronic Theses and Dissertations
This study aims to prepare theranostic nanoparticles (NPs) that are expected to increase cancer diagnostics and therapeutic efficacy. We prepared the NPs constituting carbon dots (CDs) as an imaging agent, folic acid as a targeting agent, doxorubicin (DOX), or gemcitabine (GEM) as chemotherapy agents. The NPs include noncovalent FA-CDs-DOX, covalent CDs-FA-DOX, and covalent FA-CDs-GEM. Through ultraviolet-visible spectroscopy, fluorescence spectroscopy, and Fourier transform-infrared spectroscopy, the fabrication of these NPs was confirmed. It was discovered that the high drug loading efficiency is the noncovalent series while the high drug loading capacity is the covalent series The in-vitro pH-dependent drug release data indicate …
Biomedical Applications And Syntheses Of Selected Anthraquinone Dyes, Richard Sirard
Biomedical Applications And Syntheses Of Selected Anthraquinone Dyes, Richard Sirard
Senior Honors Theses
Anthraquinones are aromatic organic compounds that have multiple applications in the biomedical field. Some anthraquinone-based compounds are used as fluorophores to contrast cell nuclei while others act as chemotherapeutic agents. However, there are not many fluorescent anthraquinone cell stains currently available. In this study, commercially available anthraquinone dyes, in addition to other dye families and compounds, were reviewed for their unique properties, advantages, and drawbacks. The development and characterization of three novel anthraquinone fluorophores revealed promising photophysical characteristics, like large Stokes shifts. One of the compounds, RBS3, was chosen for fixed and live cell staining and exhibited desirable biomedical properties. …
Thermal, Mechanical, And Rehealing Properties Of Cross-Linked Ionene Networks, Katelyn Lindenmeyer
Thermal, Mechanical, And Rehealing Properties Of Cross-Linked Ionene Networks, Katelyn Lindenmeyer
Honors College Theses
Polymers which contain ionic liquid groups have numerous applications in a wide variety of fields. Past research from our group has shown that IL-containing polymers which exist in covalently crosslinked networks can exhibit good ionic conductivities despite the hindrance in polymer chain mobility and relaxation. In part one of this thesis, efforts to create ionic networks which have the capability of being rehealed after exposure to an external stimulus are discussed. Thermoreversible maleimide-furan chemistry was incorporated into an imidazolium-containing ionene network. Maleimide-terminated, imidazolium-containing monomers were coupled with furan-functionalized monomers, prepared from commercially available multifunctional acrylates. Thermal, mechanical and rheological characterization …
Experimental And Theoretical Investigation Of Regioselectivity For A Series Of Ketoimines With Nuclear Magnetic Resonance Spectroscopy And Density Functional Theory, Amanda Stahl, Joseph M. Fritsch, Kelsey R. Brereton
Experimental And Theoretical Investigation Of Regioselectivity For A Series Of Ketoimines With Nuclear Magnetic Resonance Spectroscopy And Density Functional Theory, Amanda Stahl, Joseph M. Fritsch, Kelsey R. Brereton
Seaver College Research And Scholarly Achievement Symposium
A series of ketoimines bearing pendant quinolyl substituents were prepared by Schiff base condensation of 1,3-diketones with two different substituents: trifluoromethyl and an alkyl/aryl group (e.g., Me, Et, iPr,tBu, Ph. Synthetic reactions of ketoimines with varying alkyl/aryl substituents altered the distribution of regioisomers as measured in isolated yields and detected by 1H and 19F NMR spectroscopy of crude reaction mixtures. Reaction with the least sterically encumbered diketone (CF3with Me) resulted in mixture of ketoimines with virtually quantitative formation of the ketoimine resulting from quinolyl addition to the carbonyl adjacent to the alkyl substituent. …
Raising Global Awareness And Internationality In The Undergraduate Organic Chemistry Laboratory, Marissa Scilley, Michael R. Korn
Raising Global Awareness And Internationality In The Undergraduate Organic Chemistry Laboratory, Marissa Scilley, Michael R. Korn
Liberty University Research Week
Undergraduate
Applied
Acid Catalyzed Small Ring Alcohols And Alkenes: An Artistic Approach To Visualizing Relationships Between Features Produced By Uv-Visible Spectra, Madeleine Ware
Campus Research Month
Madeleine Ware
Research Description
Campus Research Day
My physical organic chemistry research was supervised by Dr. Mitch Menzmer who studies the formation of carbocation intermediates in acid-catalyzed reactions of alkylated and non-alkylated small ring alcohols. The goal of my work was to compile data and develop methods to search for relationships between the initial structures of molecules analyzed and the wavelengths of maximum absorbance for features observed within a given spectrum. In addition, my advisor from the School of Visual Art and Design, Associate Professor Marc Boyson, contributed to this process by providing insights about the way information could be …
Enantioselective Nickel-Catalyzed Alkyne-Azide Cycloaddition By Dynamic Kinetic Resolution, En Chih Liu, Joseph J. Topczewski
Enantioselective Nickel-Catalyzed Alkyne-Azide Cycloaddition By Dynamic Kinetic Resolution, En Chih Liu, Joseph J. Topczewski
Chemistry Faculty Research & Creative Works
The triazole heterocycle has been widely adopted as an isostere for the amide bond. Many native amides are α-chiral, being derived from amino acids. This makes α-N-chiral triazoles attractive building blocks. This report describes the first enantioselective triazole synthesis that proceeds via nickel-catalyzed alkyne-azide cycloaddition (NiAAC). This dynamic kinetic resolution is enabled by a spontaneous [3,3]-sigmatropic rearrangement of the allylic azide. The 1,4,5-trisubstituted triazole products, derived from internal alkynes, are complementary to those commonly obtained by the related CuAAC reaction. Initial mechanistic experiments indicate that the NiAAC reaction proceeds through a monometallic Ni complex, which is distinct from the CuAAC …
Preparation Of Perylene Bisimide Acceptors With Ethylcarboxyl And Pyrenylcyclohexyl Imide Groups, Michael Cashen Stark
Preparation Of Perylene Bisimide Acceptors With Ethylcarboxyl And Pyrenylcyclohexyl Imide Groups, Michael Cashen Stark
Honors Theses
Multiple attempts were made to deprotect TBDMS-protected (tert-butyldimethylsilyl protected) serinol and swallowtailed PBI (Compound 2), synthesized by past researcher Tarrah Frederick, to generate Compound 1. The theoretical Compound 1 product is intended for use in molecular rectification of electricity because the perylene core acts as a good acceptor with high electron affinity, and it does not require an electron donor group. Many rectification molecules are amphiphilic Donor-σ-Acceptor compounds, which allow for electron transfer through localized molecular orbitals when placed between electrodes (Langmuir-Blodgett Method). However, PBIs can transfer electrons from one electrode, through the LUMO of perylene, and to the other …
Synthesis Of Phosphindolizine, Tyler Bell
Synthesis Of Phosphindolizine, Tyler Bell
Campus Research Month
Synthesis of Phosphindolizine which hasn't been done before.
Greening Of Ferrocene Column Chromatography, Marissa Scilley, Anderson Hill, Michael R. Korn
Greening Of Ferrocene Column Chromatography, Marissa Scilley, Anderson Hill, Michael R. Korn
Liberty University Research Week
Undergraduate
Basic
Incorporating The Origin Of Life Theme In Organic Chemistry Laboratories: Analyses Of Amino Acids, Emmalyn Sarver, Michael R. Korn
Incorporating The Origin Of Life Theme In Organic Chemistry Laboratories: Analyses Of Amino Acids, Emmalyn Sarver, Michael R. Korn
Liberty University Research Week
Undergraduate
Basic
Nitro Group Reduction For Use In Organic, Cathodic Materials, Brock G. Goeden
Nitro Group Reduction For Use In Organic, Cathodic Materials, Brock G. Goeden
Honors Thesis
The industrial demand for higher capacity, light-weight battery materials has skyrocketed in recent years due to heavy investments in portable electronics, electronic vehicles, and renewable energy sources. However, rechargeable battery technology has seen little improvement since the invention of the Lithium-Ion battery in the 1980s. The low energy density of the traditionally utilized LiCoO2 cathodic material (specific capacity: 272 mAh g-1), has limited its potential to meet these increasing demands. To solve this problem, our research group is investigating new types of lightweight, organic, polymeric materials with conductive backbones as a possible replacement for the cathodic materials in Lithium-Ion batteries. …
Synthesis Of Dibenzophosphole Derivatives, Allan Roy Sison
Synthesis Of Dibenzophosphole Derivatives, Allan Roy Sison
Campus Research Month
This presentation will demonstrate how dibenzophosphole derivatives are synthesized. There will also be studies on the properties of this complex compound. Our experiment is based on previous studies on dibenzophospholes. We will be using the methods from the previous studies and we will synthesize the derivatives of the dibenzophosphole compound using other compounds such as dibromophenol.
"What Lights Up Your "Tech"? - Subtitle: Synthesis Of Polycyclic Aromatic Hydrocarbons (Pah) Using To 2,2-Dibromo-1,1-Binapthalene, Jefferd Daniel
"What Lights Up Your "Tech"? - Subtitle: Synthesis Of Polycyclic Aromatic Hydrocarbons (Pah) Using To 2,2-Dibromo-1,1-Binapthalene, Jefferd Daniel
Campus Research Month
The application of this molecule can be used eventually to add several elements like (Bromine, Chlorine, etc.) Previous done research that was conducted was in shortening the process to synthesize PAH. Since then, there has been research conducted to stabilize the compound by closing/linking two of the un-linked benzene rings.
Synthesize phosphyl-paralene, functionalize, and analyze the properties of those molecules and attach its derivatives
Synthesis Of Dibenzophospholes From Biphenyl, Claudia Velasquez
Synthesis Of Dibenzophospholes From Biphenyl, Claudia Velasquez
Campus Research Month
The aim is a direct synthesis of various diphenzylphospholes using biphenyl, phosphonic acid, and Tf2O. Successful addition of the phosphonic acid in a one step reaction would result in a more efficient production of the diphenylphospholes.
Visible Light Generation And Mechanistic Investigation Of High-Valent Metal-Oxo Species Supported By Different Ligands, Seth Ellis Klaine
Visible Light Generation And Mechanistic Investigation Of High-Valent Metal-Oxo Species Supported By Different Ligands, Seth Ellis Klaine
Masters Theses & Specialist Projects
Numerous transition metal catalysts have been designed as biomimetic model compounds for the active site of metalloenzymes found throughout Nature, most notably cytochrome P450 monooxygenases that carry out the oxidative transformations of organic substrates with near-perfect chemo-, regio-, and stereo-selectivity. The primary active oxidants in catalytic and enzymatic cycles are fleeting high-valent metal-oxo intermediates where the oxo ligand can transfer to an organic substrate in a process known as oxygen atom transfer (OAT).
In the present work, porphyrin-manganese(III), salen-chromium(III), and salenmanganese( III) derivatives were successfully synthesized and spectroscopically characterized using 1H NMR and UV-Vis spectroscopies. A facile photochemical approach was …
Synthesis And Catalytic Oxidation Of Organic Substrates By Light-Harvesting Metalloporphyrins, Christian Alcantar
Synthesis And Catalytic Oxidation Of Organic Substrates By Light-Harvesting Metalloporphyrins, Christian Alcantar
Masters Theses & Specialist Projects
note: Some notation in this abstract may not appear exactly as formatted in the thesis.
In this work, ruthenium, iron, and manganese light-harvesting metalloporphyrins have been successfully synthesized to serve as biomimetic models of the active site of Cytochrome P450 for the development of a green and efficient oxidation catalyst. The covalent introduction of light-harvesting boron-dipyrrin (BODIPY) fluorophores on the porphyrin macrocycle allows for the absorption of a broader range of visible light in addition to that captured by the porphyrin aromatic system alone. It is expected that this core-antenna system will increase the absorbed light energy and transfer it …
Use Of Anthraquinone Derivatives And Methods Of Efficient Syntheses, Alex Crespo
Use Of Anthraquinone Derivatives And Methods Of Efficient Syntheses, Alex Crespo
Senior Honors Theses
While the bromination of aromatic compounds is a well-researched topic, AQ and hydroxy substituted AQ derivatives, with two carbonyl groups acting as strong deactivators for electrophilic substitution, are notoriously difficult to brominate.11 Although there are well defined ways to brominate an AQ or hydroxy substituted AQ dating back to 1921,12 in order to synthesize more complex AQ derivatives, a method for halogenating AQ derivatives already bonded to more complicated or unstable functional groups is needed in order for the compound to carry out desirable activities. This represents an area of great need in research. The purpose of this …
Novel Synthetic Transformations Targeting Δ-Valerolactone And Isocoumarin, Joshua Paul Van Houten
Novel Synthetic Transformations Targeting Δ-Valerolactone And Isocoumarin, Joshua Paul Van Houten
LSU Doctoral Dissertations
The purpose of this dissertation is to describe the efforts undertaken to develop synthetic methodology targeting δ-valerolactone and isocoumarin. At the onset, an introduction to the δ-valerolactone and isocoumarin is given. Relevant examples of δ-valerolactone being utilized in the production of materials of biological and industrial application are then discussed. Following, current methods for forming δ-valerolactone are presented. After, an introduction to isocoumarin is begun. Current methods for producing isocoumarin are then discussed.
The results and discussion section of this dissertation will focus on two methods that were explored with the goal of producing α-acyl-δ-valerolactone with two different substitution patterns. …
Indolizine Donor-Based Dyes For Applications In Fluorescence Biological Imaging, William Meador
Indolizine Donor-Based Dyes For Applications In Fluorescence Biological Imaging, William Meador
Honors Theses
NIR emissive fluorophores are intensely researched due to their potential to replace modern imaging procedures. Many molecular strategies have been employed in the literature to optimize fluorophores for deeper NIR absorption and emission, biocompatibility, and higher fluorescence quantum yields. Amongst the fluorophores studied to date, proaromatic indolizine donors are attractive alternatives to traditional alkyl amine and indoline based donors due to their 1) lower energy absorption and emission facilitated by proaromaticity, 2) large Stokes shifts due to increased dihedral angles about the π-system, 3) ease of functionalization and capacity for bioconjugation at the phenyl ring, and 4) potential for further …
Review Of Chemoselective Reagent Based-Breath Analysis Techniques, Madeline F. Mccloud
Review Of Chemoselective Reagent Based-Breath Analysis Techniques, Madeline F. Mccloud
Grawemeyer Colloquium Papers
Volatile organic compounds (VOCs) pose a threat due to the negative effects of many compounds on human health. VOCs of interest are specific carbonyl compounds produced exogenously and endogenously, resultant of industrial pollution and diseases such as cancer. High concentrations of these carbonyl compounds are found in exhaled breath are linked to cancer, therefore non-invasive breath tests would prove beneficial for cancer diagnosis. Usage of chemoselective cationic reagents allows for efficient testing of these concentrations. The development of these breath tests is detailed in the report.
Methylation Of The D2 Dopamine Receptor Affects Binding With The Human Regulatory Proteins Par-4 And Calmodulin, Alexander Bowitch, Ansuman Sahoo, Andrea M. Clark, Christiana Ntangka, Krishna K. Raut, Paul Gollnick, Michael C. Yu, Steven M. Pascal, Sarah E. Walker, Denise M. Ferkey
Methylation Of The D2 Dopamine Receptor Affects Binding With The Human Regulatory Proteins Par-4 And Calmodulin, Alexander Bowitch, Ansuman Sahoo, Andrea M. Clark, Christiana Ntangka, Krishna K. Raut, Paul Gollnick, Michael C. Yu, Steven M. Pascal, Sarah E. Walker, Denise M. Ferkey
Chemistry & Biochemistry Faculty Publications
No abstract provided.
Mechanism Of Action Of Dihydropteridine Reductase, Gabriela Arias De La Rosa
Mechanism Of Action Of Dihydropteridine Reductase, Gabriela Arias De La Rosa
Dissertations, Theses, and Capstone Projects
Human dihydropteridine reductase is an enzyme that transfers a hydride from NADH to reduce quinonoid 7,8-dihydropterin (qBH2) to 5,6,7,8-tetrahydropterin (BH4), which is a cofactor important in the production of neurotransmitters.DHPR deficiency causes a drastic form of the neurological genetic disease phenylketonuria (PKU) that does not benefit from a phenylalanine-free diet.From site-directed mutagenesis studies, mostly on Rat DHPR, we know that certain residues are important for cofactor binding, substrate binding, and hydride transfer; however, there are still some questions about how DHPR works, particularly, because there is not a crystal structure of the tertiary complex: What is …
Interactions Of Organic Fluorophores With Plasmonic Surface Lattice Resonances, Robert J. Collison
Interactions Of Organic Fluorophores With Plasmonic Surface Lattice Resonances, Robert J. Collison
Dissertations, Theses, and Capstone Projects
It is common knowledge that metals, alloys and pure elements alike, are lustrous and reflective, the more so when a metal surface is flat, polished, and free from oxidation and surface fouling. However, some metals reflect visible light, in the 380 nm to 740 nm range of wavelengths, much more strongly than others. In particular, some metals reflect wavelengths in certain portions of the ultraviolet (UV), visible, and near-infrared (NIR) regime, let us say 200 nm to 2000 nm, while absorbing light strongly in other segments of this range. There are several factors that account for this difference between various …
Using The Marcus Inverted Region And Artificial Cofactors To Create A Charge Separated State In De Novo Designed Proteins, Eskil Me Andersen
Using The Marcus Inverted Region And Artificial Cofactors To Create A Charge Separated State In De Novo Designed Proteins, Eskil Me Andersen
Dissertations, Theses, and Capstone Projects
To create an efficient de novo photosynthetic protein it is important to create long lived charge separated states. Achieving stable charge separation leads to an increase in the efficiency of the photosynthetic reaction which in turn leads to higher yields of end products, such as biofuels, electrical charge, or synthetic chemicals. In an attempt to create charge separated states in de novo proteins we hypothesized that we could engineer the free energy gaps in the proteins from excited primary donor (PD) to acceptor (A), and A back to ground state PD such that the forward electron transfer (ET) would be …
Design And Synthesis Of Non-Xanthone Structural Analogs Of Α-Mangostin, Maryam Foroozmehr
Design And Synthesis Of Non-Xanthone Structural Analogs Of Α-Mangostin, Maryam Foroozmehr
Theses and Dissertations
α-Mangostin belongs to a class of polyphenolic compounds called xanthones. The potential pharmacological effects such as anti-bacterial and anti-cancer effects of α-mangostin have made it an important natural product for medicinal chemistry evaluation. During this thesis research, we have designed and synthesized a series of non-xanthone analogs of α-mangostin for medicinal chemistry evaluation. A commercially available starting material, methyl-4-methoxysalicylate was used to synthesize these non-xanthone analogs. The analogs were designed as more flexible derivatives compared to the tricyclic motif within α-mangostin yet retain the hydroxybenzoate scaffold. Through a one-pot chemical synthesis, with relatively high yield (70%), we prepared eight different …
Photoassisted Synthesis Of Complex Polyheterocycles Via Rational Design Of Tailored Photoprecursors, Tina Alanna Holt
Photoassisted Synthesis Of Complex Polyheterocycles Via Rational Design Of Tailored Photoprecursors, Tina Alanna Holt
Electronic Theses and Dissertations
Natural products remain the most common source for drug leads, although diversity-oriented synthesis of unnatural complex molecules is gaining momentum. Our lab has been developing experimentally simple and straightforward approaches to complex molecular architectures via photochemical reactions involving a minimal number of experimental steps. In order to achieve this, photoprecursors were assembled via high yielding reactions. Next, we deployed photoinduced cycloadditions to create complex 3-dimentional structures. Lastly, with this obtained primary photoproduct, post-photochemical transformations were used to further grow its scaffold complexity.
One method to increase scaffold complexity is the [4+2] intramolecular cycloadditions of azaxylylenes, which are developed through standard …
Synthesis Of Cysteine-Tyrosine Crosslink, Samuel Braak, Michael Rettstatt, David Benson
Synthesis Of Cysteine-Tyrosine Crosslink, Samuel Braak, Michael Rettstatt, David Benson
Summer Research
Some posttranslationally-modified protein tyrosines, such as the crosslink between cysteine and tyrosine (Cys-Tyr) provide sites for reversible oxidation These crosslinks are formed by an adjacent, redox active metal center when reacted with O2 . While galactose oxidation was among the first documented cys-ty crosslinks, cross linked tyrosine PTM’s have three major functions.
The Photophysical Properties Of Grevillone (6- Hydroxycoumarin) And Methylgrevillone (6-Hydroxy-4- Methyl-Coumarin), Leah H. Knoor, Hyemin Seo, Liam Hoogewerf, George Du Laney, Isaac Jonker, Mark Muyskens
The Photophysical Properties Of Grevillone (6- Hydroxycoumarin) And Methylgrevillone (6-Hydroxy-4- Methyl-Coumarin), Leah H. Knoor, Hyemin Seo, Liam Hoogewerf, George Du Laney, Isaac Jonker, Mark Muyskens
Summer Research
Grevillone (L) and methylgrevillone (R) are two of many natural compounds called coumarins. Coumarins are useful as antioxidants, antivirals, and more.