Arthur J. Elliott
Arthur J. Elliott publishes mostly in Organic Chemistry, Molecular Biology and Physical and Theoretical Chemistry, on topics such as Synthesis and Characterization of Heterocyclic Compounds, Synthesis and Reactivity of Heterocycles and Synthesis and Biological Evaluation.
- World rank
- #1,459,869 of 7,710,434 ranked researchers
- Rank in United States
- #459,054 of 1,627,098
- Works
- 38
- Citations
- 1.3k
- Citations per work
- 33.7
What does Arthur J. Elliott research?
Arthur J. Elliott's work is mostly in Chemistry (67%), Biochemistry, Genetics and Molecular Biology (19%), Medicine (3%).
Their six largest subfields, inside their fields and domains; the grey slice is everything else they publish. The interactive view splits every one of their works down to single topics.
The fields and subfields, with their numbers
- Physical Sciences2669.2%
- Chemistry2667.3%
- Materials Science11.9%
- Life Sciences820.6%
- Everything else37.4%
- Health Sciences12.8%
- Medicine12.8%
- 1Organic Chemistry64% of their works
- 2Molecular Biology19% of their works
- 3Physical and Theoretical Chemistry4% of their works
- 4Infectious Diseases3% of their works
- 5Pharmaceutical Science2% of their works
- 6Materials Chemistry2% of their works
Research topics
- Synthesis and Characterization of Heterocyclic Compounds
- Synthesis and Reactivity of Heterocycles
- Synthesis and Biological Evaluation
- Biochemical and Molecular Research
- Phenothiazines and Benzothiazines Synthesis and Activities
- Synthesis and Reactions of Organic Compounds
- Synthesis and biological activity
- Chemical Reaction Mechanisms
Which keywords describe Arthur J. Elliott's research?
The keywords of their largest research topics: Synthesis, Biological Evaluation, Heterocyclic Compounds, Molecular Docking, Antimicrobial Activity, Anticancer, Antimicrobial and Catalyst.
- Vascular Targeting Agents
- Nucleophilicity
- Phenothiazines
- Nucleotide Metabolism
- Enzyme Regulation
- Quinoxaline
- Triazines
- Drug Discovery
- Medicinal Chemistry
- Catalyst
- Anticancer
- Molecular Docking
- Biological Evaluation
- Synthesis
- Heterocyclic Compounds
- Antimicrobial Activity
- Antimicrobial
- Anticancer Agents
- Bioactivity
- Indolizines
- Derivatives
- Biological Activities
- Imidazoles
- Oxazolones
- Acidity Scales
- Tubulin Inhibitors
Size is their works in the topics tagged with each word, from their 8 largest topics. Each links to the topic it comes from most. The words come from the keyword list OpenAlex gives each topic, not from the text of the papers, so a word can appear that none of the papers uses.
All 26 words, with their numbers
- Synthesis435 topics
- Biological Evaluation293 topics
- Heterocyclic Compounds253 topics
- Molecular Docking202 topics
- Antimicrobial Activity192 topics
- Anticancer172 topics
- Antimicrobial172 topics
- Catalyst162 topics
- Anticancer Agents152 topics
- Medicinal Chemistry152 topics
- Bioactivity101 topic
- Drug Discovery101 topic
- Indolizines101 topic
- Triazines101 topic
- Derivatives91 topic
- Quinoxaline91 topic
- Biological Activities71 topic
- Enzyme Regulation71 topic
- Imidazoles71 topic
- Nucleotide Metabolism71 topic
- Oxazolones71 topic
- Phenothiazines71 topic
- Acidity Scales61 topic
- Nucleophilicity61 topic
- Tubulin Inhibitors61 topic
- Vascular Targeting Agents61 topic
Where does Arthur J. Elliott work?
Arthur J. Elliott's main affiliation in the publication record is BioCryst Pharmaceuticals (United States), United States.
How many publications and citations does Arthur J. Elliott have?
OpenAlex counts 38 works and 1,281 citations for Arthur J. Elliott, an h-index of 16, ranking #1,459,869 of 7,710,434 researchers worldwide on the quality score.
Ranked on field-normalised citation excellence (50%), output (30%) and citations (20%). Counts come from OpenAlex author records, which occasionally merge different people who share a name or split one person into several.
Papers, co-authors, who cited this work and researchers on the nearest topics have tabs of their own, above. Is this your page? Claim it with your ORCID iD, or request a correction or removal.
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