2012 - Fellow of the American Chemical Society
2004 - Fellow of the American Association for the Advancement of Science (AAAS)
1993 - Fellow of Alfred P. Sloan Foundation
The scientist’s investigation covers issues in Stereochemistry, Organic chemistry, Schmidt reaction, Intramolecular force and Total synthesis. Many of his research projects under Stereochemistry are closely connected to Phenyl group with Phenyl group, tying the diverse disciplines of science together. His Organic chemistry study frequently draws connections to adjacent fields such as Medicinal chemistry.
His work in Schmidt reaction covers topics such as Intramolecular reaction which are related to areas like Stereocenter. In general Intramolecular force, his work in Lepadiformine is often linked to Diene linking many areas of study. His Total synthesis research is multidisciplinary, incorporating elements of Aspidospermidine, Sparteine and Stereoisomerism.
His primary areas of study are Stereochemistry, Organic chemistry, Schmidt reaction, Intramolecular force and Medicinal chemistry. The concepts of his Stereochemistry study are interwoven with issues in Ring and Regioselectivity. His biological study deals with issues like Combinatorial chemistry, which deal with fields such as Peptidomimetic.
A large part of his Intramolecular force studies is devoted to Intramolecular reaction. His Medicinal chemistry research incorporates elements of Azide, Lewis acids and bases and Alkyl. Jeffrey Aubé combines subjects such as Ketone, Nucleophile and Iminium with his study of Azide.
Jeffrey Aubé mostly deals with Cancer research, Organic chemistry, Biochemistry, Stereochemistry and Combinatorial chemistry. His research integrates issues of Cancer cell, Cancer, Metastasis, Cell and RNA-binding protein in his study of Cancer research. His is involved in several facets of Organic chemistry study, as is seen by his studies on Acylation, Catalysis, Intramolecular force, Hexafluoro-2-propanol and Schmidt reaction.
Azide is closely connected to Nucleophile in his research, which is encompassed under the umbrella topic of Schmidt reaction. His study connects Mycobacterium tuberculosis and Biochemistry. His Combinatorial chemistry research is multidisciplinary, relying on both Structure–activity relationship and Drug discovery.
Structure–activity relationship, Pharmacology, κ-opioid receptor, Agonist and Organic chemistry are his primary areas of study. His research in Structure–activity relationship intersects with topics in Mitochondrial permeability transition pore, Mitochondrion, Drug discovery and Virology. His Drug discovery research focuses on subjects like Lepadiformine, which are linked to Combinatorial chemistry.
His Organic chemistry research focuses on Intramolecular force, Friedel–Crafts reaction, Reagent, Hexafluoro-2-propanol and Acylation. His Intramolecular force study which covers Catalysis that intersects with Functional group, Molecule, Enantiomer and Stereochemistry. His work carried out in the field of Azide brings together such families of science as Schmidt reaction and Nucleophile.
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The internal quaternary ammonium receptor site of Shaker potassium channels
Kathleen L. Choi;Craig Mossman;Jeffrey Aubé;Gary Yellen.
Improvement of oral peptide bioavailability: Peptidomimetics and prodrug strategies
Giovanni M. Pauletti;Giovanni M. Pauletti;Sanjeev Gangwar;Teruna J. Siahaan;Jeffrey Aubé.
Advanced Drug Delivery Reviews (1997)
Intramolecular Schmidt Reaction of Alkyl Azides
Jeffrey Aube;Gregory L. Milligan.
Journal of the American Chemical Society (1991)
Intramolecular Schmidt Reactions of Alkyl Azides with Ketones: Scope and Stereochemical Studies
Gregory L. Milligan;Craig J. Mossman;Jeffrey Aube.
Journal of the American Chemical Society (1995)
Chemistry of Bridged Lactams and Related Heterocycles
Michal Szostak;Jeffrey Aubé.
Chemical Reviews (2013)
First Asymmetric Total Synthesis of (+)-Sparteine
Brenton T. Smith;John A. Wendt;John A. Wendt;Jeffrey Aube.
Organic Letters (2002)
Syntheses of the Stemona Alkaloids (±)-Stenine, (±)-Neostenine, and (±)-13-Epineostenine Using a Stereodivergent Diels–Alder/Azido-Schmidt Reaction
Kevin J. Frankowski;Jennifer E. Golden;Yibin Zeng;Yao Lei.
Journal of the American Chemical Society (2008)
Biased agonists of the kappa opioid receptor suppress pain and itch without causing sedation or dysphoria
Tarsis F. Brust;Jenny Morgenweck;Susy A. Kim;Jamie H. Rose.
Science Signaling (2016)
Development of Functionally Selective, Small Molecule Agonists at Kappa Opioid Receptors
Lei Zhou;Kimberly M. Lovell;Kevin J. Frankowski;Stephen R. Slauson.
Journal of Biological Chemistry (2013)
Characterization of a Cdc42 protein inhibitor and its use as a molecular probe.
Lin Hong;S. Ray Kenney;Genevieve K. Phillips;Denise S. Simpson.
Journal of Biological Chemistry (2013)
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