Maurice Brookhart
Maurice Brookhart publishes mostly in Organic Chemistry, Inorganic Chemistry and Process Chemistry and Technology, on topics such as Organometallic Complex Synthesis and Catalysis, Asymmetric Hydrogenation and Catalysis and Synthetic Organic Chemistry Methods.
- World rank
- #47,941 of 7,710,434 ranked researchers
- Rank in United States
- #18,498 of 1,627,098
- Works
- 485
- Citations
- 41k
- Citations per work
- 83.9
What does Maurice Brookhart research?
Maurice Brookhart's work is mostly in Chemistry (71%), Chemical Engineering (8%), Materials Science (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 Sciences39982.2%
- Chemistry34571.1%
- Chemical Engineering387.9%
- Materials Science163.2%
- Everything else8617.8%
- 1Organic Chemistry52% of their works
- 2Inorganic Chemistry16% of their works
- 3Process Chemistry and Technology6% of their works
- 4Materials Chemistry3% of their works
- 5Physical and Theoretical Chemistry2% of their works
- 6Catalysis2% of their works
Research topics
- Organometallic Complex Synthesis and Catalysis
- Asymmetric Hydrogenation and Catalysis
- Synthetic Organic Chemistry Methods
- Carbon dioxide utilization in catalysis
- Catalytic Cross-Coupling Reactions
- Cyclopropane Reaction Mechanisms
- Organoboron and organosilicon chemistry
- Inorganic and Organometallic Chemistry
Which keywords describe Maurice Brookhart's research?
The keywords of their largest research topics: Hydrogenation, Catalysis, Organometallic Chemistry, Polymerization, Bond Activation, Transition Metal, Transition Metal Complexes and Asymmetric Catalysis.
- Functional Group Transformations
- Frustrated Lewis Pairs
- Carbene Chemistry
- Cross-Coupling Reactions
- Chemical Synthesis
- Ruthenium Catalysts
- Enantioselective Synthesis
- Asymmetric Catalysis
- Transition Metal
- Polymerization
- Catalysis
- Hydrogenation
- Organometallic Chemistry
- Bond Activation
- Transition Metal Complexes
- Chiral Ligands
- Olefin Metathesis
- Carbon Dioxide
- Organic Synthesis
- Palladium-Catalyzed
- Cyclopropanation
- Metal-Free Hydrogen Activation
- Metal Complexes
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 23 words, with their numbers
- Hydrogenation4473 topics
- Catalysis3804 topics
- Organometallic Chemistry3122 topics
- Polymerization3122 topics
- Bond Activation2381 topic
- Transition Metal2381 topic
- Transition Metal Complexes1732 topics
- Asymmetric Catalysis1361 topic
- Chiral Ligands1361 topic
- Enantioselective Synthesis1122 topics
- Olefin Metathesis741 topic
- Ruthenium Catalysts741 topic
- Carbon Dioxide731 topic
- Chemical Synthesis731 topic
- Organic Synthesis722 topics
- Cross-Coupling Reactions401 topic
- Palladium-Catalyzed401 topic
- Carbene Chemistry381 topic
- Cyclopropanation381 topic
- Frustrated Lewis Pairs371 topic
- Metal-Free Hydrogen Activation371 topic
- Functional Group Transformations321 topic
- Metal Complexes321 topic
Where does Maurice Brookhart work?
Maurice Brookhart's main affiliation in the publication record is University of North Carolina at Chapel Hill, United States.
How many publications and citations does Maurice Brookhart have?
OpenAlex counts 485 works and 40,678 citations for Maurice Brookhart, an h-index of 95, ranking #47,941 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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