Faculty

Institution

Unit

Venue

Alan J. Shusterman

Reed College

Affiliations

Mathematical and Natural Sciences

Chemistry

NoneAlan J. Shusterman is currently serving as a Chemistry faculty at Reed College.

Honors

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Experiences

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Education

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Alan J. Shusterman

Reed College

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chemistry organic chemistry biochemistry toxicology physical organic chemistry chemical sciences chemical engineering organic chemistry frontier medicinal chemistry chemical biology analytical toxicology organic process research chemical synthesis molecular science regulatory toxicology molecular structure pharmacology environmental toxicology drug discovery in vitro toxicology enzyme inhibition biochemical sciences drug analysis structural chemistry general chemistry transition metal chemistry antimicrobial agents ecotoxicology toxicological mechanism heterocycle chemistry pharmaceutical chemistry radical (chemistry) organometallic catalysis inhibitory activity structural composition mutagenesis chromatographic analysis liquid chromatography spectra-structure correlation surface reactivity alkene metathesis toxicological aspect toxicology testing anti-cancer agents experimental toxicology derivative (chemistry) reaction process reaction intermediates stereoselective synthesis structure-activity relationship heteroaromatic nitro compounds molecular orbital energies qsar model radical-based toxicity dry-column flash chromatography spectroscopic observation tungsten-carbene-alkene intermediate cyclopropane formation benzyl alcohols rapidly dividing cells qsar analysis radical reaction ring-opening reaction

Notable Scholarly Works

Notable Federal Grants

Collaborators

Stereochemistry and Mechanism of the Ring-Opening Reaction of Cyclopropylenones With Licu(Me) 2. Organometallics (2012)

Charles P. CaseyMark C. CesaAlan J. Shusterman

ring-opening reactionchemical synthesistransition metal chemistryorganometallic catalysischemistryreaction processheterocycle chemistrystereoselective synthesisreaction intermediatesorganometallic chemistryorganic synthesis

Limob, an Unsymmetrical Nonaromatic Orthoborate Salt for Nonaqueous Solution Electrochemical Applications. Journal of The Electrochemical Society (2004)

chemical sciencesenergy chemistryorganic chemistry frontiergreen chemistryelectrochemical engineeringchemical engineeringfuel cellselectroanalytical chemistryenergy storage materialssustainable chemistrychemistryorganic chemistryelectrocatalystsadvanced energy materialelectrochemical energy conversionelectrochemistry

Synthesis, Cytotoxicity, and Qsar Analysis of X-Thiophenols in Rapidly Dividing Cells. Chemical Research in Toxicology (2003)

toxicologynatural product researchqsar analysispharmaceutical chemistrytoxicological mechanismnatural productsdrug analysisanti-cancer agentsmedicinal chemistrybiochemistrybioactive compoundsexperimental toxicologypharmacologyrapidly dividing cellsdrug discoveryin vitro toxicology

Qsar for the Cytotoxicity of 2-Alkyl or 2,6-Dialkyl, 4-X-Phenols: The Nature of the Radical Reaction. Journal of the Chemical Society Perkin Transactions 2 (2002)

future medicinal chemistrypharmacognosyradical reactionbiochemistrymedicinal chemistryderivative (chemistry)chemistrypharmacologyorganic chemistrydrug discoveryradical (chemistry)organic process research

Structures of Orthoborate Anions and Physical Properties of Their Lithium Salt Nonaqueous Solutions. Journal of The Electrochemical Society (2002)

chemical sciencesinorganic chemistryelectrochemical engineeringinorganic chemistry frontierchemical structurestructural chemistrychemical engineeringcrystal engineeringenergy storage materialschemistryenergy storagephysical organic chemistryadvanced energy materialmolecular structureelectrochemical energy conversionmaterials scienceelectrochemistry

Teaching Chemistry With Electron Density Models. 2. Can Atomic Charges Adequately Explain Electrostatic Potential Maps?. The Chemical Educator (2000)

chemical physicsquantum chemistryphysicscomputational physicscomputational chemistryphysical chemistryatomic physicstheoretical chemistryelectron configurationmolecular scienceelectroanalytical chemistrychemistryscience advancemolecular physicsmolecular modelsdensity functional theory

Toxicology of Benzyl Alcohols: A Qsar Analysis. Chemosphere (2000)

toxicologytoxicological aspecttoxicological mechanismdrug analysisanalytical toxicologybenzyl alcoholsmedicinal chemistryalcohol (drug)pharmacologytoxicology testing

On the Toxicity of Phenols to Fast Growing Cells. a Qsar Model for a Radical-Based Toxicity. Journal of the Chemical Society Perkin Transactions 2 (1999)

toxicologynatural product researchtoxicological mechanismradical-based toxicityqsar modelbiochemistrychemical biologybioactive compoundspharmacologyradical (chemistry)in vitro toxicology

Dry-Column Flash Chromatography. Journal of Chemical Education (1997)

biological engineeringdrug analysisanalytical chemistrychromatographychromatographic analysisliquid chromatographymass spectrometrydry-column flash chromatography

Teaching Chemistry With Electron Density Models. Journal of Chemical Education (1997)

chemical engineeringquantum chemistrycomputational chemistrychemistrychemistry educationgeneral chemistrydensity functional theory

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Alan J. Shusterman

Reed College

Affiliations

Mathematical and Natural Sciences

Chemistry

NoneAlan J. Shusterman is currently serving as a Chemistry faculty at Reed College.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Alan J. Shusterman

Reed College

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

Stereochemistry and Mechanism of the Ring-Opening Reaction of Cyclopropylenones With Licu(Me) 2. Organometallics (2012)

Charles P. CaseyMark C. CesaAlan J. Shusterman

Limob, an Unsymmetrical Nonaromatic Orthoborate Salt for Nonaqueous Solution Electrochemical Applications. Journal of The Electrochemical Society (2004)

Synthesis, Cytotoxicity, and Qsar Analysis of X-Thiophenols in Rapidly Dividing Cells. Chemical Research in Toxicology (2003)

Qsar for the Cytotoxicity of 2-Alkyl or 2,6-Dialkyl, 4-X-Phenols: The Nature of the Radical Reaction. Journal of the Chemical Society Perkin Transactions 2 (2002)

Structures of Orthoborate Anions and Physical Properties of Their Lithium Salt Nonaqueous Solutions. Journal of The Electrochemical Society (2002)

Teaching Chemistry With Electron Density Models. 2. Can Atomic Charges Adequately Explain Electrostatic Potential Maps?. The Chemical Educator (2000)

Toxicology of Benzyl Alcohols: A Qsar Analysis. Chemosphere (2000)

toxicologytoxicological aspecttoxicological mechanismdrug analysisanalytical toxicologybenzyl alcoholsmedicinal chemistryalcohol (drug)pharmacologytoxicology testing

On the Toxicity of Phenols to Fast Growing Cells. a Qsar Model for a Radical-Based Toxicity. Journal of the Chemical Society Perkin Transactions 2 (1999)

toxicologynatural product researchtoxicological mechanismradical-based toxicityqsar modelbiochemistrychemical biologybioactive compoundspharmacologyradical (chemistry)in vitro toxicology

Dry-Column Flash Chromatography. Journal of Chemical Education (1997)

biological engineeringdrug analysisanalytical chemistrychromatographychromatographic analysisliquid chromatographymass spectrometrydry-column flash chromatography

Teaching Chemistry With Electron Density Models. Journal of Chemical Education (1997)

chemical engineeringquantum chemistrycomputational chemistrychemistrychemistry educationgeneral chemistrydensity functional theory

1
2
3
10 / page