What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Enzyme
His primary areas of investigation include Stereochemistry, Carbocation, Molecule, Quantum chemical and Organic chemistry.
He interconnects Quantum chemistry, Allylic rearrangement and Biosynthesis in the investigation of issues within Stereochemistry.
His study in Carbocation is interdisciplinary in nature, drawing from both Delocalized electron, Terpene, Active site, Enzyme and Terpene biosynthesis.
The Stereoisomerism research Dean J. Tantillo does as part of his general Molecule study is frequently linked to other disciplines of science, such as Aminoquinolines, therefore creating a link between diverse domains of science.
His studies deal with areas such as Hydride and Alkyl as well as Quantum chemical.
His studies in Terpene synthase integrate themes in fields like Computational chemistry, Photochemistry and Reactivity.
His most cited work include:
- Computational Prediction of 1H and 13C Chemical Shifts: A Useful Tool for Natural Product, Mechanistic, and Synthetic Organic Chemistry (579 citations)
- Small Molecule Signaling Agents: The Integrated Chemistry and Biochemistry of Nitrogen Oxides, Oxides of Carbon, Dioxygen, Hydrogen Sulfide, and Their Derived Species (230 citations)
- Redox chemistry and chemical biology of H2S, hydropersulfides, and derived species: implications of their possible biological activity and utility. (215 citations)
What are the main themes of his work throughout his whole career to date?
Dean J. Tantillo focuses on Stereochemistry, Computational chemistry, Carbocation, Organic chemistry and Catalysis.
His research in Stereochemistry intersects with topics in Cycloaddition, Molecule, Quantum chemical and Biosynthesis, Enzyme.
Dean J. Tantillo has included themes like Intramolecular force and Pericyclic reaction in his Cycloaddition study.
His Computational chemistry study combines topics in areas such as Reaction mechanism, Sigmatropic reaction, Photochemistry and Chemical shift.
The Carbocation study combines topics in areas such as Terpene biosynthesis, Terpene and Potential energy surface.
His research links Combinatorial chemistry with Catalysis.
He most often published in these fields:
- Stereochemistry (35.62%)
- Computational chemistry (21.90%)
- Carbocation (19.53%)
What were the highlights of his more recent work (between 2017-2021)?
- Stereochemistry (35.62%)
- Computational chemistry (21.90%)
- Density functional theory (12.14%)
In recent papers he was focusing on the following fields of study:
Dean J. Tantillo spends much of his time researching Stereochemistry, Computational chemistry, Density functional theory, Chemical physics and Carbocation.
His Stereochemistry research integrates issues from ATP synthase, Enzyme and Catalysis, Stereoselectivity.
His ATP synthase study also includes fields such as
- Terpene that intertwine with fields like Docking,
- Biosynthesis together with Natural product and Ring.
His research integrates issues of Stereoisomerism, Quantum chemical and Chemical shift in his study of Computational chemistry.
His study in Chemical shift is interdisciplinary in nature, drawing from both Conformational isomerism, Molecule, Scaling and Carbon-13 NMR.
His research investigates the connection between Chemical physics and topics such as Selectivity that intersect with issues in Potential energy surface and Intramolecular force.
Between 2017 and 2021, his most popular works were:
- The Value of Universally Available Raw NMR Data for Transparency, Reproducibility, and Integrity in Natural Product Research (32 citations)
- Diverged Plant Terpene Synthases Reroute the Carbocation Cyclization Path towards the Formation of Unprecedented 6/11/5 and 6/6/7/5 Sesterterpene Scaffolds (26 citations)
- Synthesis and Structure Revision of Dichrocephones A and B. (17 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Enzyme
Dean J. Tantillo mostly deals with Stereochemistry, Chemical physics, Density functional theory, ATP synthase and Combinatorial chemistry.
His biological study spans a wide range of topics, including Carbocation, Ring, Enantioselective synthesis and Stereoselectivity.
His study on Density functional theory is covered under Computational chemistry.
His studies deal with areas such as Conformational isomerism and Karplus equation as well as Computational chemistry.
Dean J. Tantillo interconnects Mutagenesis, Biosynthesis, Terpene, Bicyclic molecule and Diterpene in the investigation of issues within ATP synthase.
Dean J. Tantillo has included themes like Alcohol, Deoxygenation, Mechanism, Reactivity and Bond formation in his Combinatorial chemistry study.
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