Andrew G. Myers mostly deals with Organic chemistry, Stereochemistry, Enantioselective synthesis, Medicinal chemistry and Yield. His research integrates issues of Combinatorial chemistry, Methyl thioglycolate, Adduct and Neocarzinostatin chromophore in his study of Stereochemistry. His Enantioselective synthesis study also includes fields such as
His Medicinal chemistry study combines topics from a wide range of disciplines, such as Heck reaction, Decarboxylative cross-coupling and Nanotechnology. The various areas that Andrew G. Myers examines in his Yield study include A-site, Benzoic acid, Cycloaddition and Trifluoromethanesulfonate. He has researched Alkyl in several fields, including Lithium chloride, Pseudoephedrine and Chiral auxiliary.
His main research concerns Stereochemistry, Organic chemistry, Combinatorial chemistry, Medicinal chemistry and Enantioselective synthesis. His study focuses on the intersection of Stereochemistry and fields such as Neocarzinostatin chromophore with connections in the field of Thiol and Methyl thioglycolate. His work investigates the relationship between Organic chemistry and topics such as Pseudoephedrine that intersect with problems in Chiral auxiliary.
His work on Coupling reaction expands to the thematically related Medicinal chemistry. Enantioselective synthesis connects with themes related to Yield in his study. His Alkylation research integrates issues from Amino acid, Diastereomer, Amide, Hydrolysis and Alkyl.
Andrew G. Myers focuses on Stereochemistry, Organic chemistry, Combinatorial chemistry, Stereoisomerism and Antibiotics. His Stereochemistry research is multidisciplinary, relying on both Alkylation, Aldol reaction, Enantioselective synthesis and Stereoselectivity. When carried out as part of a general Organic chemistry research project, his work on Reagent, Substrate, Coupling reaction and Electrophile is frequently linked to work in Mycaminose, therefore connecting diverse disciplines of study.
His work in the fields of Combinatorial chemistry, such as Trioxacarcin, overlaps with other areas such as Component. His work carried out in the field of Stereoisomerism brings together such families of science as Glycosidic bond, Ketone and Sharpless asymmetric dihydroxylation. His study in the fields of Antibacterial drug and Penicillin under the domain of Antibiotics overlaps with other disciplines such as Development economics and Human health.
Stereochemistry, Combinatorial chemistry, Organic chemistry, Drug discovery and Sequence are his primary areas of study. His specific area of interest is Stereochemistry, where Andrew G. Myers studies Enone. Andrew G. Myers interconnects Natural product, Turn, Tetracycline antibiotics and Cyclohexenone in the investigation of issues within Combinatorial chemistry.
Electrophile, Benzoic acid, Alkene, Dimethyl sulfoxide and Reagent are the subjects of his Organic chemistry studies. Andrew G. Myers works mostly in the field of Drug discovery, limiting it down to topics relating to Antibiotics and, in certain cases, Pharmacology. The various areas that Andrew G. Myers examines in his Sequence study include Tetracycline, Isoxazole, Hydroxylation, Trioxacarcin and Stereoselectivity.
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Development of a decarboxylative palladation reaction and its use in a Heck-type olefination of arene carboxylates.
Andrew G. Myers;Daisuke Tanaka;Michael R. Mannion.
Journal of the American Chemical Society (2002)
Pseudoephedrine as a Practical Chiral Auxiliary for the Synthesis of Highly Enantiomerically Enriched Carboxylic Acids, Alcohols, Aldehydes, and Ketones
Andrew G. Myers;Bryant H. Yang;Hou Chen;Lydia McKinstry.
Journal of the American Chemical Society (1997)
On the Mechanism of the Palladium(II)-Catalyzed Decarboxylative Olefination of Arene Carboxylic Acids. Crystallographic Characterization of Non-Phosphine Palladium(II) Intermediates and Observation of Their Stepwise Transformation in Heck-like Processes
Daisuke Tanaka;Stuart P. Romeril;Andrew G. Myers.
Journal of the American Chemical Society (2005)
The Evolving Role of Chemical Synthesis in Antibacterial Drug Discovery
Peter M. Wright;Ian B. Seiple;Andrew G. Myers.
Angewandte Chemie (2014)
Thermal generation of .alpha.,3-dehydrotoluene from (Z)-1,2,4-heptatrien-6-yne
Andrew G. Myers;Elaine Y. Kuo;Nathaniel S. Finney.
Journal of the American Chemical Society (1989)
A convergent enantioselective route to structurally diverse 6-deoxytetracycline antibiotics
Mark G. Charest;Christian D. Lerner;Jason D. Brubaker;Dionicio Rhodes Siegel.
Science (2005)
Proposed structure of the neocarzinostatin chromophore-methyl thioglycolate adduct; A mechanism for the nucleophilic activation of neocarzinostatin
Andrew G. Myers.
Tetrahedron Letters (1987)
Use of Pseudoephedrine as a Practical Chiral Auxiliary for Asymmetric Synthesis
Andrew G. Myers;Bryant H. Yang;Hou Chen;James L. Gleason.
Journal of the American Chemical Society (1994)
New and Stereospecific Synthesis of Allenes in a Single Step from Propargylic Alcohols
Andrew G. Myers;Bin Zheng.
Journal of the American Chemical Society (1996)
Heck-Type Arylation of 2-Cycloalken-1-ones with Arylpalladium Intermediates Formed by Decarboxylative Palladation and by Aryl Iodide Insertion
Daisuke Tanaka;Andrew G. Myers.
Organic Letters (2004)
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