2023 - Research.com Chemistry in Japan Leader Award
Yoshinori Yamamoto mainly investigates Catalysis, Organic chemistry, Medicinal chemistry, Palladium and Cycloaddition. Yoshinori Yamamoto interconnects Nanoporous, Photochemistry, Combinatorial chemistry and Polymer chemistry in the investigation of issues within Catalysis. His Combinatorial chemistry research is multidisciplinary, incorporating elements of Annulation and Regioselectivity.
The study incorporates disciplines such as Alkyne, Intramolecular force, Lewis acids and bases and Reaction mechanism in addition to Medicinal chemistry. His Cycloaddition research focuses on subjects like Azide, which are linked to Triple bond. His Allylic rearrangement research integrates issues from Group 2 organometallic chemistry and Nucleophile.
The scientist’s investigation covers issues in Catalysis, Organic chemistry, Medicinal chemistry, Palladium and Stereochemistry. His work carried out in the field of Catalysis brings together such families of science as Combinatorial chemistry, Intramolecular force, Nanoporous and Polymer chemistry. His Allylic rearrangement, Reagent, Regioselectivity, Nucleophile and Addition reaction investigations are all subjects of Organic chemistry research.
The Medicinal chemistry study combines topics in areas such as Yield, Aldehyde, Lewis acids and bases and Aryl, Alkyl. His work on Palladium is being expanded to include thematically relevant topics such as Hydroamination. The concepts of his Stereochemistry study are interwoven with issues in Ether, Ring and Stereoselectivity.
Yoshinori Yamamoto mostly deals with Catalysis, Organic chemistry, Combinatorial chemistry, Nanoporous and Medicinal chemistry. The study of Catalysis is intertwined with the study of Polymer chemistry in a number of ways. In his research, Group, Photochemistry and Manganese is intimately related to Fullerene, which falls under the overarching field of Polymer chemistry.
As a part of the same scientific family, Yoshinori Yamamoto mostly works in the field of Nanoporous, focusing on Metal and, on occasion, Organic synthesis. His biological study spans a wide range of topics, including Aryl, Cascade, Cyanation and Alkene. The various areas that he examines in his Regioselectivity study include Nucleophile and Surface modification.
Yoshinori Yamamoto mainly focuses on Catalysis, Organic chemistry, Nanoporous, Combinatorial chemistry and Polymer chemistry. Yoshinori Yamamoto has researched Catalysis in several fields, including Fullerene and Nanotechnology. His research links Surface modification with Organic chemistry.
Yoshinori Yamamoto studied Surface modification and Rhodium that intersect with Medicinal chemistry. His Combinatorial chemistry research incorporates elements of Dimethyl sulfoxide, Photochemistry, Hydroamination and Cascade. His biological study deals with issues like Phosphine, which deal with fields such as Cyanation, Tris, Ligand, Palladium and Cyanide.
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Transition-Metal-Catalyzed Reactions in Heterocyclic Synthesis
Itaru Nakamura;Yoshinori Yamamoto.
Chemical Reviews (2004)
Coinage Metal-Assisted Synthesis of Heterocycles
Nitin T. Patil;Yoshinori Yamamoto.
Chemical Reviews (2008)
Atomic origins of the high catalytic activity of nanoporous gold
Takeshi Fujita;Takeshi Fujita;Pengfei Guan;Keith P McKenna;Keith P McKenna;Xingyou Lang.
Nature Materials (2012)
Lewis acid-catalyzed benzannulation via unprecedented [4+2] cycloaddition of o-alkynyl(oxo)benzenes and enynals with alkynes.
Naoki Asao;Tsutomu Nogami;Sunyoung Lee;Yoshinori Yamamoto.
Journal of the American Chemical Society (2003)
From σ- to π-Electrophilic Lewis Acids. Application to Selective Organic Transformations
Journal of Organic Chemistry (2007)
Transition Metal‐Catalyzed Reactions of Methylenecyclopropanes
Itaru Nakamura;Yoshinori Yamamoto.
Advanced Synthesis & Catalysis (2002)
Gold‐Catalyzed Intramolecular Carbothiolation of Alkynes: Synthesis of 2,3‐Disubstituted Benzothiophenes from (α‐Alkoxy Alkyl) (ortho‐Alkynyl Phenyl) Sulfides
Itaru Nakamura;Takuma Sato;Yoshinori Yamamoto.
Angewandte Chemie (2006)
Pd(II) acts simultaneously as a Lewis acid and as a transition-metal catalyst: synthesis of cyclic alkenyl ethers from acetylenic aldehydes.
Naoki Asao;Tsutomu Nogami;Kumiko Takahashi;Yoshinori Yamamoto.
Journal of the American Chemical Society (2002)
Copper- or Phosphine-Catalyzed Reaction of Alkynes with Isocyanides. Regioselective Synthesis of Substituted Pyrroles Controlled by the Catalyst
Shin Kamijo;Chikashi Kanazawa;Yoshinori Yamamoto.
Journal of the American Chemical Society (2005)
Selective Synthesis by Use of Lewis Acids in the Presence of Organocopper and Related Reagents. New Synthetic Methods (61)
Angewandte Chemie (1986)
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