Mamoru Tobisu mainly investigates Catalysis, Organic chemistry, Medicinal chemistry, Aryl and Combinatorial chemistry. The concepts of his Catalysis study are interwoven with issues in Photochemistry, Iodide, Polymer chemistry and Nickel. He works mostly in the field of Polymer chemistry, limiting it down to concerns involving Silylation and, occasionally, Isocyanide.
His Medicinal chemistry research is multidisciplinary, relying on both Electrophile, Palladium, Rhodium, Alkyne and Alkynylation. Mamoru Tobisu combines subjects such as Amination, Bond cleavage, Regioselectivity and Carbene with his study of Aryl. Reactivity is closely connected to Reagent in his research, which is encompassed under the umbrella topic of Combinatorial chemistry.
Catalysis, Medicinal chemistry, Aryl, Organic chemistry and Nickel are his primary areas of study. His studies in Catalysis integrate themes in fields like Combinatorial chemistry, Reagent, Carbon and Polymer chemistry. As part of one scientific family, Mamoru Tobisu deals mainly with the area of Polymer chemistry, narrowing it down to issues related to the Photochemistry, and often Oxidative addition.
His work deals with themes such as Cycloaddition, C h bond, Borylation, Carbene and Alkynylation, which intersect with Medicinal chemistry. The study incorporates disciplines such as Coupling reaction, Bond cleavage, Silylation and Reducing agent in addition to Aryl. His Nickel research integrates issues from Anisole, Atom economy and Ligand.
Mamoru Tobisu focuses on Catalysis, Medicinal chemistry, Aryl, Nickel and Organic chemistry. Mamoru Tobisu has researched Catalysis in several fields, including Combinatorial chemistry, Reagent, Carbon and Polymer chemistry. His work on Nucleophilic aromatic substitution as part of general Medicinal chemistry research is frequently linked to Allyl amine, thereby connecting diverse disciplines of science.
His Aryl research is multidisciplinary, incorporating perspectives in Moiety and Nucleophile. His Nickel research is multidisciplinary, incorporating elements of Decarbonylation, Molecule, Ligand and Photochemistry. His Photochemistry study integrates concerns from other disciplines, such as Oxidative addition, Atom economy, Bond cleavage and Activation energy.
Mamoru Tobisu mostly deals with Catalysis, Aryl, Nickel, Polymer chemistry and Reagent. His work carried out in the field of Catalysis brings together such families of science as Halide and Medicinal chemistry. His work in Medicinal chemistry covers topics such as Rhodium which are related to areas like Norbornane, Steric effects, Hydrometalation and Carbometalation.
In his study, Amination, Phenols, Decarboxylation, Leaving group and Sulfonyl is inextricably linked to Ligand, which falls within the broad field of Aryl. Mamoru Tobisu has included themes like Photochemistry and Decarbonylation in his Nickel study. When carried out as part of a general Organic chemistry research project, his work on Phosphole, Palladium, Phosphorus and Catalytic method is frequently linked to work in Substrate, therefore connecting diverse disciplines of study.
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Cross-Couplings Using Aryl Ethers via C-O Bond Activation Enabled by Nickel Catalysts.
Mamoru Tobisu;Naoto Chatani.
Accounts of Chemical Research (2015)
Catalytic reactions involving the cleavage of carbon–cyano and carbon–carbon triple bonds
Mamoru Tobisu;Naoto Chatani.
Chemical Society Reviews (2008)
Palladium-catalyzed direct ethynylation of C(sp3)-H bonds in aliphatic carboxylic acid derivatives.
Yusuke Ano;Mamoru Tobisu;Naoto Chatani.
Journal of the American Chemical Society (2011)
Nickel‐Catalyzed Cross‐Coupling of Aryl Methyl Ethers with Aryl Boronic Esters
Mamoru Tobisu;Toshiaki Shimasaki;Naoto Chatani.
Angewandte Chemie (2008)
Nickel-catalyzed reaction of arylzinc reagents with N-aromatic heterocycles: a straightforward approach to C-H bond arylation of electron-deficient heteroaromatic compounds.
Mamoru Tobisu;Isao Hyodo;Naoto Chatani.
Journal of the American Chemical Society (2009)
Modular Synthesis of Phenanthridine Derivatives by Oxidative Cyclization of 2-Isocyanobiphenyls with Organoboron Reagents†
Mamoru Tobisu;Keika Koh;Takayuki Furukawa;Naoto Chatani.
Angewandte Chemie (2012)
Ni(II)-Catalyzed Oxidative Coupling between C(sp2)–H in Benzamides and C(sp3)–H in Toluene Derivatives
Yoshinori Aihara;Mamoru Tobisu;Yoshiya Fukumoto;Naoto Chatani.
Journal of the American Chemical Society (2014)
Palladium-catalyzed direct alkynylation of C-H bonds in benzenes.
Mamoru Tobisu;Yusuke Ano;Naoto Chatani.
Organic Letters (2009)
A catalytic approach for the functionalization of C(sp3)-H bonds.
Mamoru Tobisu;Naoto Chatani.
Angewandte Chemie (2006)
Nickel-catalyzed amination of aryl pivalates by the cleavage of aryl C-O bonds.
Toshiaki Shimasaki;Mamoru Tobisu;Naoto Chatani.
Angewandte Chemie (2010)
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