What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
His primary areas of study are Organic chemistry, Catalysis, Nickel, Medicinal chemistry and Lewis acids and bases.
His work carried out in the field of Catalysis brings together such families of science as Aryl, Intramolecular force and Polymer chemistry.
His Aryl research incorporates elements of Molecule, Hydroxymethyl and Copper.
His Nickel study incorporates themes from Lewis acid catalysis, Alkylation, Pyridine, Carbene and Oxidative addition.
His Medicinal chemistry study combines topics in areas such as Regioselectivity, Ligand, Formamides, Alkyl and Silylation.
Yoshiaki Nakao interconnects Reactivity and Nitrile in the investigation of issues within Lewis acids and bases.
His most cited work include:
- Silicon-based cross-coupling reaction: an environmentally benign version (368 citations)
- A strategy for C-H activation of pyridines: direct C-2 selective alkenylation of pyridines by nickel/Lewis acid catalysis. (286 citations)
- Selective C-4 Alkylation of Pyridine by Nickel/Lewis Acid Catalysis (231 citations)
What are the main themes of his work throughout his whole career to date?
His primary scientific interests are in Catalysis, Organic chemistry, Nickel, Medicinal chemistry and Aryl.
His research in Catalysis intersects with topics in Combinatorial chemistry and Polymer chemistry.
Steric effects is closely connected to Carbene in his research, which is encompassed under the umbrella topic of Nickel.
His study in Medicinal chemistry is interdisciplinary in nature, drawing from both Oxidative addition, Ligand, Intramolecular force, Hydroxymethyl and Addition reaction.
Yoshiaki Nakao works mostly in the field of Aryl, limiting it down to topics relating to Coupling reaction and, in certain cases, Reagent, Silicon, Silicon based and Palladium catalyst, as a part of the same area of interest.
His studies in Lewis acids and bases integrate themes in fields like Pyridine, Reactivity, Nitrile and Moiety.
He most often published in these fields:
- Catalysis (70.74%)
- Organic chemistry (45.85%)
- Nickel (41.05%)
What were the highlights of his more recent work (between 2015-2021)?
- Catalysis (70.74%)
- Organic chemistry (45.85%)
- Aryl (24.89%)
In recent papers he was focusing on the following fields of study:
Yoshiaki Nakao mainly investigates Catalysis, Organic chemistry, Aryl, Polymer chemistry and Nickel.
His studies deal with areas such as Combinatorial chemistry, Aluminium and Copper as well as Catalysis.
His study in Regioselectivity and Alkene falls under the purview of Organic chemistry.
His Medicinal chemistry research extends to Aryl, which is thematically connected.
His Medicinal chemistry research is multidisciplinary, incorporating perspectives in Oxidative addition, Ligand, Amine gas treating and Reaction mechanism.
His work investigates the relationship between Nickel and topics such as Carbene that intersect with problems in Steric effects.
Between 2015 and 2021, his most popular works were:
- The Suzuki-Miyaura Coupling of Nitroarenes. (69 citations)
- para-Selective Alkylation of Benzamides and Aromatic Ketones by Cooperative Nickel/Aluminum Catalysis (69 citations)
- Reductive Cross-Coupling of Conjugated Arylalkenes and Aryl Bromides with Hydrosilanes by Cooperative Palladium/Copper Catalysis. (57 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
Catalysis, Organic chemistry, Nickel, Palladium and Medicinal chemistry are his primary areas of study.
His work in Catalysis addresses subjects such as Combinatorial chemistry, which are connected to disciplines such as Hydride.
His Aluminium, Aryl, Regioselectivity and Alkene investigations are all subjects of Organic chemistry research.
In his research on the topic of Regioselectivity, Polymer chemistry is strongly related with Lewis acids and bases.
His biological study spans a wide range of topics, including Amination and Catalytic cycle.
His Medicinal chemistry research is multidisciplinary, incorporating elements of Oxidative addition and Ligand.
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