L. VASVARI‐DEBRECZY
L. VASVARI‐DEBRECZY publishes mostly in Organic Chemistry, Molecular Biology and Spectroscopy, on topics such as Synthesis and Reactions of Organic Compounds, Synthesis and Characterization of Heterocyclic Compounds and Synthesis and Biological Evaluation.
- World rank
- #5,389,839 of 7,710,434 ranked researchers
- Rank in Hungary
- #13,807 of 25,218
- Works
- 55
- Citations
- 395
- Citations per work
- 7.2
What does L. VASVARI‐DEBRECZY research?
L. VASVARI‐DEBRECZY's work is mostly in Chemistry (88%), Biochemistry, Genetics and Molecular Biology (7%), Pharmacology, Toxicology and Pharmaceutics (1%).
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 Sciences4989.0%
- Chemistry4988.3%
- Chemical Engineering00.7%
- Life Sciences58.5%
- Everything else12.5%
- 1Organic Chemistry84% of their works
- 2Molecular Biology7% of their works
- 3Spectroscopy3% of their works
- 4Pharmaceutical Science1% of their works
- 5Catalysis1% of their works
- 6Physical and Theoretical Chemistry1% of their works
Research topics
- Synthesis and Reactions of Organic Compounds
- Synthesis and Characterization of Heterocyclic Compounds
- Synthesis and Biological Evaluation
- Synthesis of heterocyclic compounds
- Chemical Reaction Mechanisms
- Synthesis and Reactivity of Heterocycles
- Synthesis and biological activity
- Structural and Chemical Analysis of Organic and Inorganic Compounds
Which keywords describe L. VASVARI‐DEBRECZY's research?
The keywords of their largest research topics: Synthesis, Heterocycles, Biological Evaluation, Catalyst, Heterocyclic Compounds, Molecular Docking, Antimicrobial Activity and Antimicrobial.
- Tubulin Inhibitors
- Oxadiazoles
- Bioactivity
- Acidity Scales
- Annulation
- Derivatives
- Anticancer
- Oxazolones
- Medicinal Chemistry
- Antimicrobial
- Molecular Docking
- Catalyst
- Heterocycles
- Synthesis
- Biological Evaluation
- Heterocyclic Compounds
- Antimicrobial Activity
- Anticancer Agents
- Imidazoles
- Catalyzed Reactions
- Triazines
- Quinoxaline
- Ketene Dithioacetal
- Nucleophilicity
- Indolizines
- Thiadiazoles
- Vascular Targeting Agents
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 27 words, with their numbers
- Synthesis886 topics
- Heterocycles624 topics
- Biological Evaluation453 topics
- Catalyst412 topics
- Heterocyclic Compounds323 topics
- Molecular Docking272 topics
- Antimicrobial Activity262 topics
- Antimicrobial252 topics
- Anticancer Agents242 topics
- Medicinal Chemistry242 topics
- Imidazoles231 topic
- Oxazolones231 topic
- Catalyzed Reactions222 topics
- Anticancer191 topic
- Triazines191 topic
- Derivatives181 topic
- Quinoxaline181 topic
- Annulation141 topic
- Ketene Dithioacetal141 topic
- Acidity Scales91 topic
- Nucleophilicity91 topic
- Bioactivity81 topic
- Indolizines81 topic
- Oxadiazoles61 topic
- Thiadiazoles61 topic
- Tubulin Inhibitors61 topic
- Vascular Targeting Agents61 topic
Where does L. VASVARI‐DEBRECZY work?
L. VASVARI‐DEBRECZY's main affiliation in the publication record is Research and Development for Silicates and Ceramics, Hungary.
How many publications and citations does L. VASVARI‐DEBRECZY have?
OpenAlex counts 55 works and 395 citations for L. VASVARI‐DEBRECZY, an h-index of 11, ranking #5,389,839 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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