What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
The scientist’s investigation covers issues in Organic chemistry, Catalysis, Medicinal chemistry, Aryl and Transition metal.
His Catalysis study combines topics in areas such as Optically active and Copper.
His work in Medicinal chemistry addresses issues such as Stereoselectivity, which are connected to fields such as Nickel, Paraformaldehyde, Aldol condensation, Metallocene and Isocyanide.
The concepts of his Aryl study are interwoven with issues in Propargyl and Annulation.
As part of one scientific family, Eiji Shirakawa deals mainly with the area of Transition metal, narrowing it down to issues related to the Halide, and often Potassium tert-butoxide, Coupling reaction, Stereoisomerism and Derivative.
His Palladium research incorporates elements of Cationic polymerization, Polymer chemistry, Trifluoromethanesulfonate and Indium triflate.
His most cited work include:
- tert-Butoxide-mediated arylation of benzene with aryl halides in the presence of a catalytic 1,10-phenanthroline derivative. (350 citations)
- Addition of Ureas to Arynes: Straightforward Synthesis of Benzodiazepine and Benzodiazocine Derivatives (158 citations)
- Lipoxygenase-catalyzed oxygenation of arachidonylethanolamide, a cannabinoid receptor agonist (152 citations)
What are the main themes of his work throughout his whole career to date?
Eiji Shirakawa mostly deals with Catalysis, Organic chemistry, Medicinal chemistry, Aryl and Polymer chemistry.
Eiji Shirakawa has included themes like Conjugated system and Nickel in his Catalysis study.
His work deals with themes such as Regioselectivity, Iron catalyzed, Alkyl and Phosphine, which intersect with Medicinal chemistry.
Eiji Shirakawa interconnects Propargyl, Halide, Reagent and Coupling reaction in the investigation of issues within Aryl.
His Polymer chemistry study integrates concerns from other disciplines, such as Carbon, Zinc and Pyrrole derivatives.
His Palladium research incorporates themes from Oxidative addition, Ligand, Hexamethyldisilane and Combinatorial chemistry.
He most often published in these fields:
- Catalysis (65.42%)
- Organic chemistry (41.59%)
- Medicinal chemistry (31.31%)
What were the highlights of his more recent work (between 2012-2021)?
- Aryl (30.37%)
- Medicinal chemistry (31.31%)
- Coupling (8.41%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Aryl, Medicinal chemistry, Coupling, Photochemistry and Halide.
Aryl is the subject of his research, which falls under Organic chemistry.
His research combines Oxidative phosphorylation and Organic chemistry.
His study looks at the relationship between Medicinal chemistry and fields such as Hyponitrite, as well as how they intersect with chemical problems.
His Halide research is multidisciplinary, incorporating perspectives in Oxidative addition, Halogenation and Ruthenium.
Eiji Shirakawa combines subjects such as Zinc and Indium with his study of Catalysis.
Between 2012 and 2021, his most popular works were:
- Single electron transfer-induced Grignard cross-coupling involving ion radicals as exclusive intermediates (32 citations)
- Single-electron-transfer-induced coupling of arylzinc reagents with aryl and alkenyl halides. (29 citations)
- Single electron transfer-induced cross-coupling reaction of alkenyl halides with aryl Grignard reagents (22 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
Eiji Shirakawa spends much of his time researching Aryl, Photochemistry, Reagent, Coupling and Single electron.
His Aryl research includes themes of Halide and Catalysis.
His Catalysis research is multidisciplinary, relying on both Zinc and Indium.
The Photochemistry study combines topics in areas such as Zinc iodide and Propanol.
His Reagent study deals with Polymer chemistry intersecting with Alkylation, Iodide, Alkyl, Electron transfer and Diglyme.
His research ties Medicinal chemistry and Organic chemistry together.
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