D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Chemistry D-index 66 Citations 13,560 208 World Ranking 4561 National Ranking 1545

Overview

What is he best known for?

The fields of study he is best known for:

  • Organic chemistry
  • Enzyme
  • Catalysis

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

  • Enantiomer which connect with Alkylation,
  • Electrophile which intersects with area such as Stereoselectivity and Decarboxylation.

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 most cited work include:

  • Development of a decarboxylative palladation reaction and its use in a Heck-type olefination of arene carboxylates. (447 citations)
  • Pseudoephedrine as a Practical Chiral Auxiliary for the Synthesis of Highly Enantiomerically Enriched Carboxylic Acids, Alcohols, Aldehydes, and Ketones (405 citations)
  • 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 (324 citations)

What are the main themes of his work throughout his whole career to date?

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.

He most often published in these fields:

  • Stereochemistry (39.26%)
  • Organic chemistry (28.52%)
  • Combinatorial chemistry (16.30%)

What were the highlights of his more recent work (between 2009-2021)?

  • Stereochemistry (39.26%)
  • Organic chemistry (28.52%)
  • Combinatorial chemistry (16.30%)

In recent papers he was focusing on the following fields of study:

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.

Between 2009 and 2021, his most popular works were:

  • Mediator kinase inhibition further activates super-enhancer-associated genes in AML (195 citations)
  • The Evolving Role of Chemical Synthesis in Antibacterial Drug Discovery (194 citations)
  • A platform for the discovery of new macrolide antibiotics (149 citations)

In his most recent research, the most cited papers focused on:

  • Organic chemistry
  • Enzyme
  • Catalysis

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.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

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)

763 Citations

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)

701 Citations

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)

565 Citations

The Evolving Role of Chemical Synthesis in Antibacterial Drug Discovery

Peter M. Wright;Ian B. Seiple;Andrew G. Myers.
Angewandte Chemie (2014)

373 Citations

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)

366 Citations

A convergent enantioselective route to structurally diverse 6-deoxytetracycline antibiotics

Mark G. Charest;Christian D. Lerner;Jason D. Brubaker;Dionicio Rhodes Siegel.
Science (2005)

319 Citations

Proposed structure of the neocarzinostatin chromophore-methyl thioglycolate adduct; A mechanism for the nucleophilic activation of neocarzinostatin

Andrew G. Myers.
Tetrahedron Letters (1987)

306 Citations

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)

300 Citations

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)

297 Citations

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)

291 Citations

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