What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
Sakae Uemura mostly deals with Catalysis, Organic chemistry, Medicinal chemistry, Ruthenium and Palladium.
His research in Catalysis is mostly focused on Enantioselective synthesis.
Toluene, Yield, Bond cleavage, Alcohol oxidation and Pyridine are among the areas of Organic chemistry where Sakae Uemura concentrates his study.
His Medicinal chemistry research includes elements of Catalytic cycle, Vanadium, Optically active and Nucleophile.
His Ruthenium study combines topics from a wide range of disciplines, such as Organic synthesis and Homogeneous catalysis.
His Palladium study incorporates themes from Oxygen atmosphere and Alkene.
His most cited work include:
- Palladium(II)-Catalyzed Oxidation of Alcohols to Aldehydes and Ketones by Molecular Oxygen. (347 citations)
- Pd(II)−Hydrotalcite-Catalyzed Oxidation of Alcohols to Aldehydes and Ketones Using Atmospheric Pressure of Air (169 citations)
- Pd(OAc)2-catalyzed oxidation of alcohols to aldehydes and ketones by molecular oxygen (155 citations)
What are the main themes of his work throughout his whole career to date?
Sakae Uemura focuses on Catalysis, Organic chemistry, Medicinal chemistry, Palladium and Polymer chemistry.
In his study, Allylic rearrangement is inextricably linked to Substitution reaction, which falls within the broad field of Catalysis.
Yield, Chloride, Enantioselective synthesis, Reagent and Acetic acid are subfields of Organic chemistry in which his conducts study.
His Medicinal chemistry research incorporates themes from Moiety, Aryl, Alkyl, Acetonitrile and Nucleophile.
His study in Palladium is interdisciplinary in nature, drawing from both Bond cleavage, Ligand, Catalytic cycle, Toluene and Oxygen.
The Polymer chemistry study combines topics in areas such as Photochemistry and Tetrahydrofuran.
He most often published in these fields:
- Catalysis (54.82%)
- Organic chemistry (46.18%)
- Medicinal chemistry (44.52%)
What were the highlights of his more recent work (between 2002-2010)?
- Catalysis (54.82%)
- Organic chemistry (46.18%)
- Medicinal chemistry (44.52%)
In recent papers he was focusing on the following fields of study:
Sakae Uemura mostly deals with Catalysis, Organic chemistry, Medicinal chemistry, Ruthenium and Substitution reaction.
His Catalysis research integrates issues from Combinatorial chemistry, Yield and Polymer chemistry.
His Yield research is multidisciplinary, relying on both Indole test and Oxygen.
He has researched Medicinal chemistry in several fields, including Moiety, Ligand, Ring, Catalytic cycle and Carbene.
His Ruthenium study integrates concerns from other disciplines, such as Regioselectivity, Alcohol, Reactivity, Cationic polymerization and Stereoselectivity.
His studies in Palladium integrate themes in fields like Alcohol oxidation and Bond cleavage.
Between 2002 and 2010, his most popular works were:
- Palladium-catalyzed asymmetric arylation, vinylation, and allenylation of tert-cyclobutanols via enantioselective C-C bond cleavage. (151 citations)
- Novel Ruthenium‐ and Platinum‐Catalyzed Sequential Reactions: Synthesis of Tri‐ and Tetrasubstituted Furans and Pyrroles from Propargylic Alcohols and Ketones (142 citations)
- Ruthenium-catalyzed propargylic substitution reactions of propargylic alcohols with oxygen-, nitrogen-, and phosphorus-centered nucleophiles. (128 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
His main research concerns Catalysis, Organic chemistry, Ruthenium, Medicinal chemistry and Enantioselective synthesis.
Sakae Uemura regularly links together related areas like Substitution reaction in his Catalysis studies.
His study in Yield, Alkylation, Chloride, Palladium and Reagent is done as part of Organic chemistry.
His studies deal with areas such as Homogeneous catalysis, Alcohol, Electrophilic aromatic substitution, Reactivity and Combinatorial chemistry as well as Ruthenium.
His Medicinal chemistry research is multidisciplinary, incorporating perspectives in Regioselectivity, Ligand, Ring, Stereochemistry and Nucleophile.
His study explores the link between Enantioselective synthesis and topics such as Acetone that cross with problems in Nucleophilic substitution.
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