His primary areas of study are Catalysis, Organic chemistry, Alkyl, Medicinal chemistry and Polymer chemistry. His research combines Intramolecular force and Catalysis. His work deals with themes such as Reagent, Halide, Coupling reaction and Photochemistry, which intersect with Alkyl.
His Reagent research is multidisciplinary, incorporating elements of Yield, Non catalytic and Aluminium. His Medicinal chemistry research integrates issues from Aryl and Aldehyde. His Polymer chemistry research includes themes of Carbon and Polymer, Monomer.
Nobuaki Kambe mostly deals with Catalysis, Organic chemistry, Medicinal chemistry, Alkyl and Reagent. Nobuaki Kambe has included themes like Aryl and Polymer chemistry in his Catalysis study. Organic chemistry is a component of his Carbon monoxide, Selenium, Sulfur, Silylation and Aliphatic compound studies.
His Medicinal chemistry research is multidisciplinary, incorporating perspectives in Intramolecular force, Moiety, Stereochemistry, Bond cleavage and Stereoselectivity. In his work, Ligand is strongly intertwined with Halide, which is a subfield of Alkyl. The concepts of his Reagent study are interwoven with issues in Combinatorial chemistry, 1,3-Butadiene and Nickel.
Nobuaki Kambe mainly focuses on Catalysis, Medicinal chemistry, Alkyl, Aryl and Reagent. His Catalysis research entails a greater understanding of Organic chemistry. His Medicinal chemistry research incorporates elements of Copper catalyzed, Cleavage, Regioselectivity, Bond cleavage and Stereochemistry.
His Alkyl study combines topics from a wide range of disciplines, such as Halide, Alkylation, Electrophile and Pyrene. The study incorporates disciplines such as Carbon–carbon bond, Carbon, 1,3-Butadiene and Steric effects in addition to Reagent. Intramolecular force is closely connected to Rhodium in his research, which is encompassed under the umbrella topic of Polymer chemistry.
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Pd-catalyzed cross-coupling reactions of alkyl halides
Nobuaki Kambe;Takanori Iwasaki;Jun Terao.
Chemical Society Reviews (2011)
Cross-Coupling Reaction of Alkyl Halides with Grignard Reagents Catalyzed by Ni, Pd, or Cu Complexes with π-Carbon Ligand(s)
Jun Terao;Nobuaki Kambe.
Accounts of Chemical Research (2008)
Nickel-catalyzed cross-coupling reaction of grignard reagents with alkyl halides and tosylates: remarkable effect of 1,3-butadienes.
Jun Terao;Hideyuki Watanabe;Aki Ikumi;Hitoshi Kuniyasu.
Journal of the American Chemical Society (2002)
Ni- or Cu-Catalyzed Cross-Coupling Reaction of Alkyl Fluorides with Grignard Reagents
Jun Terao;Aki Ikumi;Hitoshi Kuniyasu;Nobuaki Kambe.
Journal of the American Chemical Society (2003)
Palladium-catalyzed addition and carbonylative addition of diaryl disulfides and diselenides to terminal acetylenes
Hitoshi Kuniyasu;Akiya Ogawa;Shin Ichiro Miyazaki;Ilhyong Ryu.
Journal of the American Chemical Society (1991)
The first example of transition-metal-catalyzed addition of aromatic thiols to acetylenes
Hitoshi Kuniyasu;Akiya Ogawa;Ken Ichiro Sato;Ilhyong Ryu.
Journal of the American Chemical Society (1992)
Copper‐Catalyzed Cross‐Coupling Reaction of Grignard Reagents with Primary‐Alkyl Halides: Remarkable Effect of 1‐Phenylpropyne
Jun Terao;Hirohisa Todo;Shameem Ara Begum;Hitoshi Kuniyasu.
Angewandte Chemie (2007)
Nickel‐Catalyzed Cross‐Coupling Reaction of Alkyl Halides with Organozinc and Grignard Reagents with 1,3,8,10‐Tetraenes as Additives
Jun Terao;Hirohisa Todo;Hideyuki Watanabe;Aki Ikumi.
Angewandte Chemie (2004)
Lithium‐Tellurium Exchange: A New Entry to Organolithium Compounds
Tomoki Hiiro;Nobuaki Kambe;Akiya Ogawa;Noritaka Miyoshi.
Angewandte Chemie (1987)
Self-Organized Interconnect Method for Molecular Devices
Masateru Taniguchi;Yoshihiro Nojima;Kazumichi Yokota;Jun Terao.
Journal of the American Chemical Society (2006)
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