S
Seijiro Matsubara
Researcher at Kyoto University
Publications - 336
Citations - 5372
Seijiro Matsubara is an academic researcher from Kyoto University. The author has contributed to research in topics: Catalysis & Cycloaddition. The author has an hindex of 38, co-authored 327 publications receiving 4813 citations. Previous affiliations of Seijiro Matsubara include University of Tokyo.
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Nickel-catalyzed intermolecular carboiodination of alkynes with aryl iodides.
Toshifumi Takahashi,Daiki Kuroda,Toru Kuwano,Yuji Yoshida,Takuya Kurahashi,Seijiro Matsubara +5 more
TL;DR: Nickel-catalyzed intermolecular carboiodination of alkynes with aryl iodides to form highly substituted and functionalized alkenyl iodides has been developed.
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Reaction Pathway of Methylenation of Carbonyl Compounds with Bis(iodozincio)methane
Mutsumi Sada,Shinsuke Komagawa,Masanobu Uchiyama,Masami Kobata,Tsuyoshi Mizuno,Kiitiro Utimoto,Koichiro Oshima,Seijiro Matsubara +7 more
TL;DR: The present computational/theoretical study concluded that the methylenation reaction with gem-dizinc reagent proceeds as a two-step reaction, that is, methylene addition (RDS) and olefination.
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Organocatalytic enantio- and diastereoselective cycloetherification via dynamic kinetic resolution of chiral cyanohydrins.
TL;DR: A concise organocatalytic cycloetherification for the highly enantio- and diastereoselective synthesis of tetrahydropyrans involving simultaneous construction of two chiral centres, one of which is fully substituted.
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H–D exchange reaction on benzene ring of polystyrene in hydrothermal deuterium oxide with platinum(IV) oxide catalyst
TL;DR: Benzene rings of polystyrene samples are labelled with deuterium oxide and catalytic amount of platinum(iv) oxide under hydrothermal conditions.
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"Naked" Lithium Cation: Strongly Activated Metal Cations Facilitated by Carborane Anions.
TL;DR: The superactivated lithium cation has greatly enhanced Lewis acidic character and mediates various organic reactions such as carbonyl-ene reaction, NBS-bromination of unactivated aromatics, and Friedel-Crafts alkylation, which are not promoted by conventional lithium salts.