His main research concerns Catalysis, Organic chemistry, Photochemistry, Polymer chemistry and Palladium. His biological study spans a wide range of topics, including Reagent, Medicinal chemistry, Nickel and Halide. His Photodissociation study in the realm of Photochemistry interacts with subjects such as Ultraviolet.
His research integrates issues of Inorganic chemistry and Transition metal in his study of Polymer chemistry. He works mostly in the field of Palladium, limiting it down to topics relating to Aliphatic compound and, in certain cases, Carboxylic acid and Diketone. Makoto Kumada combines subjects such as Denticity, Aryl, Stereochemistry and Hydrosilylation with his study of Phosphine.
The scientist’s investigation covers issues in Organic chemistry, Medicinal chemistry, Catalysis, Photochemistry and Polymer chemistry. His study in the field of Trimethylsilyl is also linked to topics like Cleavage. The Catalysis study combines topics in areas such as Halide, Alkyl and Nickel.
His work carried out in the field of Photochemistry brings together such families of science as Intramolecular force, Optically active, Methanol and Silylene. As a part of the same scientific study, Makoto Kumada usually deals with the Polymer chemistry, concentrating on Enantioselective synthesis and frequently concerns with Combinatorial chemistry. His studies in Phosphine integrate themes in fields like Aryl and Coupling reaction.
His main research concerns Organic chemistry, Catalysis, Palladium, Medicinal chemistry and Polymer chemistry. His Catalysis study combines topics from a wide range of disciplines, such as Halide and Metal. While the research belongs to areas of Palladium, Makoto Kumada spends his time largely on the problem of Optically active, intersecting his research to questions surrounding Hydrosilylation.
His Medicinal chemistry research incorporates themes from Reactivity, Bromide, Ring and Coupling reaction. His Polymer chemistry research focuses on Enantioselective synthesis and how it connects with Transition metal. The study incorporates disciplines such as Aryl, Silylation and Nickel in addition to Phosphine.
His primary areas of study are Palladium, Catalysis, Polymer chemistry, Aliphatic compound and Reagent. His studies deal with areas such as Medicinal chemistry and Enantioselective synthesis as well as Palladium. In Medicinal chemistry, he works on issues like Ethylamine, which are connected to Ring.
His study on Catalysis is covered under Organic chemistry. His Aliphatic compound research is multidisciplinary, relying on both Solvent effects, Stereochemistry, Organic synthesis and Optically active. In his study, Alkyl and Primary is strongly linked to Halide, which falls under the umbrella field of Reagent.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Selective carbon-carbon bond formation by cross-coupling of Grignard reagents with organic halides. Catalysis by nickel-phosphine complexes
Kohei Tamao;Koji Sumitani;Makoto Kumada.
Journal of the American Chemical Society (1972)
Nickel-phosphine complex-catalyzed Grignard coupling—II : Grignard coupling of heterocyclic compounds
K. Tamao;S. Kodama;I. Nakajima;M. Kumada.
Tetrahedron (1982)
Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II): an effective catalyst for cross-coupling of secondary and primary alkyl Grignard and alkylzinc reagents with organic halides
Tamio Hayashi;Mitsuo Konishi;Yuji Kobori;Makoto Kumada.
Journal of the American Chemical Society (1984)
Nickel-phosphine complex-catalyzed Grignard coupling. I. Cross-coupling of alkyl, aryl, and alkenyl Grignard reagents with aryl and alkenyl halides: General scope and limitations.
Kohei Tamao;Koji Sumitani;Yoshihisa Kiso;Michio Zembayashi.
Bulletin of the Chemical Society of Japan (1976)
Asymmetric Synthesis Catalyzed by Chiral Ferrocenylphosphine–Transition Metal Complexes. I. Preparation of Chiral Ferrocenylphosphines
Tamio Hayashi;Takaya Mise;Motoo Fukushima;Masahiro Kagotani.
Bulletin of the Chemical Society of Japan (1980)
Silafunctional compounds in organic synthesis. Part 20. Hydrogen peroxide oxidation of the silicon-carbon bond in organoalkoxysilanes
Kohei Tamao;Neyoshi Ishida;Tatsu Tanaka;Makoto Kumada.
Organometallics (1983)
Asymmetric synthesis catalyzed by chiral ferrocenylphosphine-transition metal complexes. 2. Nickel- and palladium-catalyzed asymmetric Grignard cross-coupling
Tamio Hayashi;Mitsuo Konishi;Motoo Fukushima;Takaya Mise.
Journal of the American Chemical Society (1982)
Asymmetric synthesis catalyzed by transition-metal complexes with functionalized chiral ferrocenylphosphine ligands
Tamio Hayashi;Makoto Kumada.
Accounts of Chemical Research (1982)
Alkyl group isomerization in the cross-coupling reaction of secondary alkyl Grignard reagents with organic halides in the presence of nickel-phosphine complexes as catalysts
Kohei Tamao;Yoshihisa Kiso;Koji Sumitani;Makoto Kumada.
Journal of the American Chemical Society (1972)
Asymmetric synthesis catalyzed by chiral ferrocenylphosphine-transition metal complexes. 5. Palladium-catalyzed asymmetric allylation of active methine compounds
Tamio Hayashi;Koichi Kanehira;Toshiya Hagihara;Makoto Kumada.
Journal of Organic Chemistry (1988)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
Kyoto University
Hiroshima University
National Tsing Hua University
Tokyo University of Science
Kyoto University
Tokyo Institute of Technology
Osaka Metropolitan University
Hangzhou Normal University
Nagasaki Institute of Applied Science
Ritsumeikan University
University of Central Florida
Widya Mandala Surabaya Catholic University
University of Rochester Medical Center
Brookhaven National Laboratory
University of Santiago de Compostela
Nara Institute of Science and Technology
University of Genoa
University of Melbourne
University of Rochester Medical Center
University of Montreal
Mayo Clinic
McGill University
Federal University of Toulouse Midi-Pyrénées
University of Gothenburg
University College London
National Observatory of Athens