| Journal Articles: 23 results |
|
|
Synthesis of Albendazole Metabolite: Characterization and HPLC Determination Graciela Mahler, Danilo Davyt, Sandra Gordon, Marcelo Incerti, Ivana Núñez, Horacio Pezaroglo, Laura Scarone, Gloria Serra, Mauricio Silvera, and Eduardo Manta
In this laboratory activity, students are introduced to the synthesis of an albendazole metabolite obtained by a sulfide oxidation reaction. Albendazole as well as its metabolite, albendazole sulfoxide, are used as anthelmintic drugs. The oxidation reagent is H2O2 in acetic acid. The reaction is environmental friendly, fast, and proceeds with high yield. The crude reaction is analyzed by HPLC chromatography to determine purity. The simplicity of the experiment allows students to study chiral concepts, physicochemical and spectroscopic properties of the compounds, and HPLC determinations.
Mahler, Graciela; Davyt, Danilo; Gordon, Sandra; Incerti, Marcelo; Núñez, Ivana; Pezaroglo, Horacio; Scarone, Laura; Serra, Gloria; Silvera, Mauricio; Manta, Eduardo. J. Chem. Educ. 2008, 85, 1652.
Chirality / Optical Activity |
Drugs / Pharmaceuticals |
HPLC |
Medicinal Chemistry |
Organosulfur Compounds |
Oxidation / Reduction |
Synthesis
|
Dimethyl Sulfoxide Jay A. Young
The hazards of dimethyl sulfoxide are discussed.
Young, Jay A. J. Chem. Educ. 2008, 85, 629.
Laboratory Management
|
Synthesis of Quaternary Ammonium Salts of Tricyclic Cationic Drugs: A One-Pot Synthesis for the Bioorganic Chemistry Laboratory Linda S. Brunauer, Abid C. Mogannam, Won B. Hwee, and James Y. Chen
Describes a one-pot conversion of tricyclic cationic drugs to their quaternary ammonium forms for a widely used bioactive drug, chlorpromazine, a phenothiazine-based antipsychotic. The conversion of parent drug to the methylated form was evaluated by qualitatively measuring its ability to induce alterations in the shape of mammalian erythrocytes.
Brunauer, Linda S.; Mogannam, Abid C.; Hwee, Won B.; Chen, James Y. J. Chem. Educ. 2007, 84, 1992.
Amines / Ammonium Compounds |
Bioorganic Chemistry |
Drugs / Pharmaceuticals |
IR Spectroscopy |
Microscale Lab |
NMR Spectroscopy |
Synthesis |
Thin Layer Chromatography
|
Using Ozone in Organic Chemistry Lab: The Ozonolysis of Eugenol Bruce M. Branan, Joshua T. Butcher, and Lawrence R. Olsen
This organic laboratory involves the ozonolysis of eugenol (clove oil) followed by a reductive workup that generates an aldehyde easily identified by its NMR and IR spectra.
Branan, Bruce M.; Butcher, Joshua T.; Olsen, Lawrence R. J. Chem. Educ. 2007, 84, 1979.
Aldehydes / Ketones |
Gases |
IR Spectroscopy |
Laboratory Equipment / Apparatus |
Natural Products |
NMR Spectroscopy |
Synthesis |
Oxidation / Reduction
|
Determination of Solvent Effects on Keto—Enol Equilibria of 1,3-Dicarbonyl Compounds Using NMR A. Gilbert Cook and Paul M. Feltman
Expands the classic physical chemistry experiment using of proton NMR to determine the equilibrium position of tautomeric 1,3-dicarbonyl compounds in various solvents.
Cook, A. Gilbert; Feltman, Paul M. J. Chem. Educ. 2007, 84, 1827.
Aldehydes / Ketones |
Equilibrium |
Hydrogen Bonding |
Molecular Modeling |
Molecular Properties / Structure |
NMR Spectroscopy |
Solutions / Solvents |
Thermodynamics
|
Keeping Your Students Awake: Facile Microscale Synthesis of Modafinil, a Modern Anti-Narcoleptic Drug Evangelos Aktoudianakis, Rui Jun Lin, and Andrew P. Dicks
Describes the microscale preparation of modafinil, a pharmaceutical recently approved for the treatment of narcolepsy, by a sulfide oxidation reaction. An unusual feature of modafinil is the presence of a chiral sulfoxide functionality where a sulfur atom acts as a stereocenter, demonstrating that atoms other than carbon can act as centers of chirality.
Aktoudianakis, Evangelos; Lin, Rui Jun; Dicks, Andrew P. J. Chem. Educ. 2006, 83, 1832.
Chirality / Optical Activity |
Drugs / Pharmaceuticals |
Synthesis |
Mechanisms of Reactions |
IR Spectroscopy |
NMR Spectroscopy |
Microscale Lab |
Stereochemistry
|
3,5-Diarylisoxazoles: Individualized Three-Step Synthesis and Isomer Determination Using 13C NMR or Mass Spectroscopy Chad E. Stephens and Reem K. Arafa
Describes the three-step synthesis and definitive characterization of a 3,5-diarylisoxazole via the chalcone and chalcone dibromide. The project is individualized with regard to compound purification, characterization, and literature searches as each student prepares a differently substituted chalcone.
Stephens, Chad E.; Arafa, Reem K. J. Chem. Educ. 2006, 83, 1336.
Alkenes |
Heterocycles |
IR Spectroscopy |
Mass Spectrometry |
NMR Spectroscopy |
Synthesis |
Spectroscopy
|
Regioselective Synthesis of a Stereodefined Heterocyclic Push–Pull Alkene. 1H NMR Studies and Two-Dimensional TLC Illustrating Z/E Isomerization Rade Markovi, Marija Baranac, Vesna Jovanovi, and Zdravko Dambaski
Facile and direct regioselective synthesis of the 4-oxothiazolidine derivative from inexpensive chemicals as an example of kinetic versus thermodynamic control is described.
Markovi, Rade; Baranac, Marija; Jovanovi, Vesna; Dambaski, Zdravko. J. Chem. Educ. 2004, 81, 1026.
Heterocycles |
Alkenes |
Stereochemistry |
Synthesis |
NMR Spectroscopy
|
Acid–Base Titrations in Nonaqueous Solvents and Solvent Mixtures Lajos Barcza and Ágnes Buvári-Barcza
Discussion of acid-base theory, the role of hydrogen bonding in acid-base reactions, and promoting, leveling, and differentiating effects.
Barcza, Lajos; Buvári-Barcza, Ágnes. J. Chem. Educ. 2003, 80, 822.
Acids / Bases |
Equilibrium |
Solutions / Solvents |
Titration / Volumetric Analysis |
Enrichment / Review Materials |
Hydrogen Bonding |
Lewis Acids / Bases |
Brønsted-Lowry Acids / Bases
|
Protecting Groups in Carbohydrate Chemistry Sigthór Pétursson
The most important protecting groups in carbohydrate chemistry are reviewed. The paper is aimed at those beginning to specialize in synthetic carbohydrate chemistry and at teachers with other specialties who wish to go beyond the content of general organic chemistry textbooks.
Petursson, Sigthor. J. Chem. Educ. 1997, 74, 1297.
Carbohydrates |
Molecular Properties / Structure |
Synthesis
|
Diastereospecific Synthesis of an Epoxide: An Introductory Experiment in Organic Synthetic and Mechanistic Chemistry James A. Ciaccio
A two-step epoxide synthesis that can be presented to students in the form of two mechanistic "puzzles" that probe the stereoselectivity of two important reactions: halohydrin formation from alkenes and epoxide formation via intramolecular Williamson ether synthesis.
Ciaccio, James A. J. Chem. Educ. 1995, 72, 1037.
Stereochemistry |
Molecular Properties / Structure |
Mechanisms of Reactions |
Synthesis |
Epoxides |
Alkenes
|
Other Publications on C6Cl6 and C2Cl6 Keiter, Richard L.
Previous JCE articles on the formation of C6Cl6 and C2Cl6.
Keiter, Richard L. J. Chem. Educ. 1995, 72, 956.
Synthesis
|
Information sources for organic chemistry, 3 Somerville, Arleen N.
This article is the third in a series that provides ready-to-use lecture material about organic chemistry information sources, a chart that links sources with questions which is suitable for distribution to students, and a set of practice questions.
Somerville, Arleen N. J. Chem. Educ. 1992, 69, 379.
Solutions / Solvents
|
A new method for the oxidation of 4-phenylurazole to 4-phenyltriazolinedione. Mallakpour, Shadpour E.
The procedures describe the synthesis of 4-phenyl-urazole from ethyl carbazate and then the oxidation of the urazole with NO2-N2O4 to yield 4-phenyl-1,2,4-trizoline-3,5-dione.
Mallakpour, Shadpour E. J. Chem. Educ. 1992, 69, 238.
Oxidation / Reduction |
Aldehydes / Ketones |
Synthesis |
Aromatic Compounds
|
The solvation of halide ions and its chemical significance Sharpe, Alan G.
Most of this article is concerned with structural and thermodynamic aspects of halide ion solvation, first by water and the by other solvents.
Sharpe, Alan G. J. Chem. Educ. 1990, 67, 309.
Solutions / Solvents |
Thermodynamics |
Ionic Bonding
|
The use of fluoromethanes in organic synthesis Everett, T. Stephen
A review of advances in selective fluorination; mechanisms and applications of fluoromethanes in organic synthesis.
Everett, T. Stephen J. Chem. Educ. 1987, 64, 143.
Synthesis |
Mechanisms of Reactions
|
Phase transfer catalysis. Part II: Synthetic applications Gokel, George W.; Weber, William P.
In this month's continuation of an article, the authors have catalogued a number of illustrative examples so that the range of applicability of phase transfer catalysis will be.
Gokel, George W.; Weber, William P. J. Chem. Educ. 1978, 55, 429.
Phases / Phase Transitions / Diagrams |
Catalysis |
Aromatic Compounds |
Organometallics |
Nucleophilic Substitution |
Synthesis |
Esters |
Oxidation / Reduction |
Alkylation
|
Preparation of vanillin from eugenol and sawdust Lampman, Gary M.; Andrews, Jennifer; Bratz, Wayne; Hanssen, Otto; Kelley, Kenneth; Perry, Dana; Ridgeway, Anthony
Two procedures are described for the conversion of eugenol to vanillin.
Lampman, Gary M.; Andrews, Jennifer; Bratz, Wayne; Hanssen, Otto; Kelley, Kenneth; Perry, Dana; Ridgeway, Anthony J. Chem. Educ. 1977, 54, 776.
Synthesis |
Consumer Chemistry |
Food Science |
Mechanisms of Reactions |
Aromatic Compounds |
Oxidation / Reduction
|
Hydrogen bonding and heat of solution Friedman, Norman
An experiment that clearly illustrates the role of hydrogen bond formation and its effect on the heat of solution.
Friedman, Norman J. Chem. Educ. 1977, 54, 248.
Hydrogen Bonding |
Calorimetry / Thermochemistry |
Solutions / Solvents
|
Lyophilization apparatus Lunelli, Bruno
A method based on an easily constructed apparatus that allows laboratory-scale lyophilizations to be carried out.
Lunelli, Bruno J. Chem. Educ. 1973, 50, 577.
Laboratory Equipment / Apparatus |
Separation Science |
Phases / Phase Transitions / Diagrams |
Laboratory Management
|
Selected properties of selected solvents Nilles, George P.; Schuetz, Robert D.
Selected properties of fifty common solvents.
Nilles, George P.; Schuetz, Robert D. J. Chem. Educ. 1973, 50, 267.
Physical Properties |
Solutions / Solvents
|
Potential hazards involved in using dimethyl sulfoxide Buckley, Alan
Solutions of compounds in DMSO can present particular hazards.
Buckley, Alan J. Chem. Educ. 1965, 42, 674.
Solutions / Solvents
|
Solvent effect on the keto-enol equilibrium of acetoacetic ester Lockwood, Karl L.
The purpose of the investigation is to introduce students to some of the factors that influence an equilibrium constant.
Lockwood, Karl L. J. Chem. Educ. 1965, 42, 481.
Solutions / Solvents |
Equilibrium
|
|
