Hideki Yorimitsu spends much of his time researching Organic chemistry, Catalysis, Medicinal chemistry, Palladium and Aryl. Organic chemistry is represented through his Halide, Reagent, Allylic rearrangement, Regioselectivity and Alcohol research. His study in Catalysis is interdisciplinary in nature, drawing from both Cobalt and Polymer chemistry.
His studies deal with areas such as Ether, Adduct and Alkyl as well as Medicinal chemistry. His biological study spans a wide range of topics, including Combinatorial chemistry, Reaction conditions, Indole test and Microwave irradiation. Hideki Yorimitsu has researched Aryl in several fields, including Oxidative addition, Sulfanyl, Helicene and Sulfur.
Hideki Yorimitsu focuses on Catalysis, Organic chemistry, Medicinal chemistry, Aryl and Palladium. His Catalysis research incorporates elements of Reagent, Polymer chemistry, Cobalt, Halide and Alkyl. His Reagent research is multidisciplinary, incorporating perspectives in Hydride, Triethylborane, Gallium trichloride, Gallium and Combinatorial chemistry.
His study in Stereoselectivity, Allylic rearrangement, Nickel, Chloride and Organic synthesis is done as part of Organic chemistry. His work carried out in the field of Medicinal chemistry brings together such families of science as Yield, Alcohol, Ether and Silylation. Hideki Yorimitsu regularly ties together related areas like Carbene in his Aryl studies.
His primary areas of study are Catalysis, Medicinal chemistry, Aryl, Organic chemistry and Palladium. Hideki Yorimitsu interconnects Combinatorial chemistry, Organosulfur compounds, Borylation and Polymer chemistry in the investigation of issues within Catalysis. His Combinatorial chemistry research incorporates themes from Reagent, Intramolecular force, Benzene and Photoredox catalysis.
His study in Medicinal chemistry is interdisciplinary in nature, drawing from both Regioselectivity, Alkylation, Nucleophile and Alkyl. Hideki Yorimitsu has researched Aryl in several fields, including Electrophile, Sulfur, Carbene, Coupling and Chloride. While the research belongs to areas of Palladium, Hideki Yorimitsu spends his time largely on the problem of Transmetalation, intersecting his research to questions surrounding Non-covalent interactions.
His scientific interests lie mostly in Catalysis, Medicinal chemistry, Organic chemistry, Aryl and Palladium. His research in Catalysis intersects with topics in Nickel, Organosulfur compounds and Intramolecular force, Stereochemistry, Benzofuran. The various areas that he examines in his Medicinal chemistry study include Yield, Alkylation, Ring, Reactivity and Hydrogen bond.
As part of his studies on Organic chemistry, Hideki Yorimitsu often connects relevant areas like Fluorescence. His Aryl research includes elements of Combinatorial chemistry, Electrophile, Coupling and Carbene. His Palladium study combines topics from a wide range of disciplines, such as Methyl triflate and Borylation.
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Cobalt-catalyzed Heck-type reaction of alkyl halides with styrenes.
Yousuke Ikeda;Tomoaki Nakamura;Hideki Yorimitsu;Koichiro Oshima.
Journal of the American Chemical Society (2002)
Nickel-catalyzed carboxylation of organozinc reagents with CO2.
Hidenori Ochiai;Minsul Jang;Koji Hirano;Hideki Yorimitsu.
Organic Letters (2008)
Cobalt-Catalyzed Trimethylsilylmethylmagnesium-Promoted Radical Alkenylation of Alkyl Halides: A Complement to the Heck Reaction
Walter Affo;Hirohisa Ohmiya;Takuma Fujioka;Yousuke Ikeda.
Journal of the American Chemical Society (2006)
Powerful solvent effect of water in radical reaction: Triethylborane-induced atom-transfer radical cyclization in water
Hideki Yorimitsu;Tomoaki Nakamura;Hiroshi Shinokubo;Koichiro Oshima.
Journal of the American Chemical Society (2000)
Cobalt-catalyzed tandem radical cyclization and cross-coupling reaction: Its application to benzyl-substituted heterocycles
Katsuyu Wakabayashi;Hideki Yorimitsu;Koichiro Oshima.
Journal of the American Chemical Society (2001)
Recent Progress in Asymmetric Allylic Substitutions Catalyzed by Chiral Copper Complexes
Hideki Yorimitsu;Koichiro Oshima.
Angewandte Chemie (2005)
Cobalt‐Catalyzed Coupling Reaction of Alkyl Halides with Allylic Grignard Reagents
Takashi Tsuji;Hideki Yorimitsu;Koichiro Oshima.
Angewandte Chemie (2002)
Cobalt(diamine)-catalyzed cross-coupling reaction of alkyl halides with arylmagnesium reagents: stereoselective constructions of arylated asymmetric carbons and application to total synthesis of AH13205.
Hirohisa Ohmiya;Hideki Yorimitsu;Koichiro Oshima.
Journal of the American Chemical Society (2006)
Stereoselective hydrothiolation of alkynes catalyzed by cesium base: Facile access to (Z)-1-alkenyl sulfides
Azusa Kondoh;Kazuaki Takami;Hideki Yorimitsu;Koichiro Oshima.
Journal of Organic Chemistry (2005)
Cobalt-catalyzed cross-coupling reactions of alkyl halides with allylic and benzylic Grignard reagents and their application to tandem radical cyclization/cross-coupling reactions.
Hirohisa Ohmiya;Takashi Tsuji;Hideki Yorimitsu;Koichiro Oshima.
Chemistry: A European Journal (2004)
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