What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
His primary scientific interests are in Catalysis, Organic chemistry, Medicinal chemistry, Rhenium and C h bond.
His Catalysis study combines topics from a wide range of disciplines, such as Intramolecular force and Indium.
His research in the fields of Molecule, Palladium and Regioselectivity overlaps with other disciplines such as Activator.
Yoichiro Kuninobu has included themes like Denticity and Functional group in his Medicinal chemistry study.
Yoichiro Kuninobu focuses mostly in the field of Rhenium, narrowing it down to topics relating to Acetylene and, in certain cases, Indene, Aldimine, Reductive elimination and Photochemistry.
His study in C h bond is interdisciplinary in nature, drawing from both Annulation, Manganese and Aldehyde.
His most cited work include:
- Insertion of polar and nonpolar unsaturated molecules into carbon-rhenium bonds generated by C-H bond activation: synthesis of phthalimidine and indene derivatives. (212 citations)
- A meta -selective C–H borylation directed by a secondary interaction between ligand and substrate (197 citations)
- Rhenium-catalyzed formation of indene frameworks via C-H bond activation: [3+2] Annulation of aromatic aldimines and acetylenes (181 citations)
What are the main themes of his work throughout his whole career to date?
Yoichiro Kuninobu mostly deals with Catalysis, Medicinal chemistry, Rhenium, Organic chemistry and Regioselectivity.
His Catalysis research integrates issues from Single bond and Polymer chemistry.
His studies in Medicinal chemistry integrate themes in fields like Yield, Manganese, Aryl, Intramolecular force and Nucleophile.
Yoichiro Kuninobu works mostly in the field of Intramolecular force, limiting it down to topics relating to Alkyl and, in certain cases, Solvent.
His research integrates issues of Acetylene, Reductive elimination, Aldimine and Indene in his study of Rhenium.
His research investigates the link between Regioselectivity and topics such as Lewis acids and bases that cross with problems in Trifluoromethylation and Borane.
He most often published in these fields:
- Catalysis (72.49%)
- Medicinal chemistry (57.64%)
- Rhenium (41.92%)
What were the highlights of his more recent work (between 2014-2021)?
- Catalysis (72.49%)
- Medicinal chemistry (57.64%)
- Regioselectivity (18.78%)
In recent papers he was focusing on the following fields of study:
His main research concerns Catalysis, Medicinal chemistry, Regioselectivity, Organic chemistry and Combinatorial chemistry.
In his works, Yoichiro Kuninobu conducts interdisciplinary research on Catalysis and Substrate.
His Medicinal chemistry research incorporates themes from Yield, Functional group, C h bond, Steric effects and Rhenium.
His Regioselectivity research is multidisciplinary, relying on both Ligand, Lewis acids and bases, Borylation, Trifluoromethylation and Nucleophile.
His Organic chemistry research focuses on Borane in particular.
His biological study deals with issues like Non-covalent interactions, which deal with fields such as Organic molecules and Transition metal.
Between 2014 and 2021, his most popular works were:
- A meta -selective C–H borylation directed by a secondary interaction between ligand and substrate (197 citations)
- Manganese- and Borane-Mediated Synthesis of Isobenzofuranones from Aromatic Esters and Oxiranes via C-H Bond Activation. (81 citations)
- Palladium-catalyzed oxirane-opening reaction with arenes via C-H bond activation (55 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
Medicinal chemistry, Catalysis, Organic chemistry, Regioselectivity and Borylation are his primary areas of study.
His Medicinal chemistry research is multidisciplinary, incorporating elements of Photochemistry, Aryl, Intramolecular force and Functional group.
As a member of one scientific family, Yoichiro Kuninobu mostly works in the field of Aryl, focusing on Aldehyde and, on occasion, C h bond.
His Palladium study, which is part of a larger body of work in Catalysis, is frequently linked to Substrate, bridging the gap between disciplines.
His Regioselectivity study incorporates themes from Trifluoromethylation, Iridium, Lewis acids and bases and Nucleophile.
His Borylation course of study focuses on Ligand and Stereochemistry, Primary, Nitrogen atom, Rhenium and Hydrogen.
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