Y
Yoshiki Nishiguchi
Researcher at Kyoto University
Publications - 6
Citations - 229
Yoshiki Nishiguchi is an academic researcher from Kyoto University. The author has contributed to research in topics: Catalysis & Moiety. The author has an hindex of 3, co-authored 6 publications receiving 207 citations.
Papers
More filters
Journal ArticleDOI
Iridium-catalyzed ring cleavage reaction of cyclobutanone O-benzoyloximes providing nitriles.
TL;DR: Iridium-catalyzed ring cleavage reaction of cyclobutanone O-benzoyloximes in the presence of 9,10-dihydroanthracene and potassium carbonate proceeds to give saturated nitriles via C-C bond fission at the sterically more hindered site.
Journal ArticleDOI
Palladium-catalyzed transformation of cyclobutanone O-benzoyloximes to nitriles via C-C bond cleavage.
TL;DR: Palladium-catalyzed transformation of cyclobutanone O-benzoyloximes to a variety of nitriles is described and the sequential reaction composed of the C-C bond cleavage and the subsequent intra- and intermolecular C- C bond formations via the corresponding alkylpalladium species is demonstrated.
Journal ArticleDOI
Ruthenium/chloride catalytic system for conjugate addition of terminal alkynes to acrylate esters
TL;DR: The addition of terminal alkynes to acrylate esters in the presence of a ruthenium catalyst and chloride sources proceeds to give the corresponding γ,δ-alkynyl ester in good yields.
Journal ArticleDOI
Ruthenium/Chloride Catalytic System for Conjugate Addition of Terminal Alkynes to Acrylate Esters.
TL;DR: The addition of terminal alkynes to acrylate esters in the presence of a ruthenium catalyst and chloride sources proceeds to give the corresponding γ,δ-alkynyl esters with good yields.
Journal ArticleDOI
Iridium-Catalyzed Ring Cleavage Reaction of Cyclobutanone O-Benzoyloximes Providing Nitriles.
TL;DR: Iridium-catalyzed ring cleavage reaction of cyclobutanone O-benzoyloximes in the presence of 9,10-dihydroanthracene and potassium carbonate proceeds to give saturated nitriles via C−C bond fission at the sterically more hindered site.