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 Organic chemistry, Catalysis, Medicinal chemistry, Stereochemistry and Helicene.
His research integrates issues of Optically active, Metal and Methylaniline in his study of Catalysis.
His Medicinal chemistry research is multidisciplinary, incorporating elements of Pauson–Khand reaction, Adduct, Silyl enol ether and Michael reaction.
His Stereochemistry study combines topics from a wide range of disciplines, such as Crystallography, Helix and Dimer.
His Helicene study combines topics in areas such as Cycloalkyne, Moiety, Chirality, Vapor pressure osmometry and Monomer.
His work in Rhodium addresses issues such as Aryl, which are connected to fields such as Bond energy, Reactivity, Sulfur and Benzene.
His most cited work include:
- ASYMMETRIC MICHAEL ADDITION OF MALONATE ANIONS TO PROCHIRAL ACCEPTORS CATALYZED BY L-PROLINE RUBIDIUM SALT (185 citations)
- Rhodium-catalyzed substitution reaction of aryl fluorides with disulfides: p-orientation in the polyarylthiolation of polyfluorobenzenes. (152 citations)
- A Catalytic Enantioselective Michael Addition of a Simple Malonate to Prochiral α,β‐Unsaturated Ketoses and Aldehydes (138 citations)
What are the main themes of his work throughout his whole career to date?
Masahiko Yamaguchi mainly investigates Organic chemistry, Catalysis, Medicinal chemistry, Rhodium and Stereochemistry.
The Catalysis study combines topics in areas such as Sulfur and Polymer chemistry.
His Medicinal chemistry research incorporates elements of Enol, Bond formation, Ketone, Triphenylphosphine and Silylation.
His Rhodium research includes elements of Aryl, Alkyl, Bond cleavage and Metathesis.
His Stereochemistry research incorporates themes from Crystallography, Optically active and Helicene.
His studies deal with areas such as Nanoparticle and Chirality as well as Helicene.
He most often published in these fields:
- Organic chemistry (40.45%)
- Catalysis (40.45%)
- Medicinal chemistry (35.73%)
What were the highlights of his more recent work (between 2014-2021)?
- Catalysis (40.45%)
- Rhodium (22.33%)
- Helicene (11.91%)
In recent papers he was focusing on the following fields of study:
His scientific interests lie mostly in Catalysis, Rhodium, Helicene, Organic chemistry and Medicinal chemistry.
His Catalysis research integrates issues from Sulfur and Polymer chemistry.
The various areas that Masahiko Yamaguchi examines in his Rhodium study include Combinatorial chemistry, Reagent and Thiazole.
His Helicene research includes elements of Chemical reaction, Helix, Oligomer, Metastability and Chirality.
In the field of Organic chemistry, his study on Aryl, Precipitation, Organic synthesis and Nucleophile overlaps with subjects such as Thesaurus.
His research investigates the link between Medicinal chemistry and topics such as Phosphine that cross with problems in Acyl group, Adduct and Flue-gas desulfurization.
Between 2014 and 2021, his most popular works were:
- Molecular switching involving metastable states: molecular thermal hysteresis and sensing of environmental changes by chiral helicene oligomeric foldamers (36 citations)
- Dynamic and Reversible Polymorphism of Self-Assembled Lyotropic Liquid Crystalline Systems Derived from Cyclic Bis(ethynylhelicene) Oligomers. (25 citations)
- Energy Aspects of Thermal Molecular Switching: Molecular Thermal Hysteresis of Helicene Oligomers. (23 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
Masahiko Yamaguchi mainly focuses on Catalysis, Helicene, Rhodium, Organic chemistry and Crystallography.
His research in Catalysis intersects with topics in Yield, Photochemistry and Medicinal chemistry.
His Medicinal chemistry study combines topics from a wide range of disciplines, such as Aryl and Phosphine.
His biological study spans a wide range of topics, including Chemical reaction, Non-equilibrium thermodynamics, Nanoparticle, Hysteresis and Metastability.
His Rhodium study frequently links to other fields, such as Polymer chemistry.
His Crystallography research integrates issues from Molecule and Stereochemistry.
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