Kazunori Nagao
Kazunori Nagao publishes mostly in Organic Chemistry, Inorganic Chemistry and Molecular Biology, on topics such as Catalytic C–H Functionalization Methods, Catalytic Cross-Coupling Reactions and Organoboron and organosilicon chemistry.
- World rank
- #331,903 of 7,710,434 ranked researchers
- Rank in Japan
- #2,921 of 383,136
- Works
- 104
- Citations
- 4.6k
- Citations per work
- 43.8
What does Kazunori Nagao research?
Kazunori Nagao's work is mostly in Chemistry (85%), Biochemistry, Genetics and Molecular Biology (7%), Pharmacology, Toxicology and Pharmaceutics (2%).
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 Sciences9086.9%
- Chemistry8985.4%
- Materials Science21.5%
- Life Sciences98.7%
- Everything else54.4%
- 1Organic Chemistry79% of their works
- 2Inorganic Chemistry6% of their works
- 3Molecular Biology6% of their works
- 4Pharmaceutical Science2% of their works
- 5Materials Chemistry2% of their works
- 6Biochemistry1% of their works
Research topics
- Catalytic C–H Functionalization Methods
- Catalytic Cross-Coupling Reactions
- Organoboron and organosilicon chemistry
- Radical Photochemical Reactions
- Sulfur-Based Synthesis Techniques
- Asymmetric Hydrogenation and Catalysis
- Chemical Synthesis and Analysis
- N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
Which keywords describe Kazunori Nagao's research?
The keywords of their largest research topics: Transition Metal Catalysis, Organic Synthesis, Transition Metal Complexes, Aryl Halides, Catalysis, Carbon–Carbon Bond Formation, C–H Activation and Cross-Coupling Reactions.
- Organometallic Chemistry
- Peptide Synthesis
- Hydrogenation
- Transition-Metal-Catalyzed
- Visible Light Photoredox Catalysis
- Asymmetric Catalysis
- Frustrated Lewis Pairs
- Cross-Coupling Reactions
- Carbon–Carbon Bond Formation
- Aryl Halides
- Organic Synthesis
- Transition Metal Catalysis
- Transition Metal Complexes
- Catalysis
- C–H Activation
- Palladium-Catalyzed
- Metal-Free Hydrogen Activation
- Electrochemical Methods
- Sulfur Bond Formation
- Chiral Ligands
- Drug Discovery
- N-Heterocyclic Carbenes
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 22 words, with their numbers
- Transition Metal Catalysis822 topics
- Organic Synthesis813 topics
- Transition Metal Complexes753 topics
- Aryl Halides552 topics
- Catalysis462 topics
- Carbon–Carbon Bond Formation451 topic
- C–H Activation451 topic
- Cross-Coupling Reactions371 topic
- Palladium-Catalyzed371 topic
- Frustrated Lewis Pairs331 topic
- Metal-Free Hydrogen Activation331 topic
- Asymmetric Catalysis292 topics
- Electrochemical Methods261 topic
- Visible Light Photoredox Catalysis261 topic
- Sulfur Bond Formation181 topic
- Transition-Metal-Catalyzed181 topic
- Chiral Ligands161 topic
- Hydrogenation161 topic
- Drug Discovery141 topic
- Peptide Synthesis141 topic
- N-Heterocyclic Carbenes131 topic
- Organometallic Chemistry131 topic
Where does Kazunori Nagao work?
Kazunori Nagao's main affiliation in the publication record is Kanazawa University, Japan.
How many publications and citations does Kazunori Nagao have?
OpenAlex counts 104 works and 4,554 citations for Kazunori Nagao, an h-index of 32, ranking #331,903 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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