Tatsuhiko Yoshino
www.pharm.hokudai.ac.jp
0000-0001-9441-9272
Hokkaido University
20 papers found
Refreshing results…
Cobalt(III)/Chiral Carboxylic Acid‐Catalyzed Enantioselective Synthesis of Benzothiadiazine‐1‐oxides via C−H Activation
1,2-Disubstituted 1,2-Dihydro-1,2,4,5-tetrazine-3,6-dione as a Dynamic Covalent Bonding Unit at Room Temperature
Cp*Rh(iii)/boron hybrid catalysis for directed C–H addition to β-substituted α,β-unsaturated carboxylic acids
Cp*RhIII/Chiral Disulfonate/CuOAc Catalyst System for the Enantioselective Intramolecular Oxyamination of Alkenes
Ruthenium(II)/Chiral Carboxylic Acid Catalyzed Enantioselective C–H Functionalization of Sulfoximines
Development of Pseudo-C2-symmetric Chiral Binaphthyl Monocarboxylic Acids for Enantioselective C(sp3)–H Functionalization Reactions under Rh(III) Catalysis
Metal-Containing Schiff Base/Sulfoxide Ligands for Pd(II)-Catalyzed Asymmetric Allylic C–H Aminations
Silane- and peroxide-free hydrogen atom transfer hydrogenation using ascorbic acid and cobalt-photoredox dual catalysis
Chemoselective Cleavage of Si–C(sp3) Bonds in Unactivated Tetraalkylsilanes Using Iodine Tris(trifluoroacetate)
Rhodium(III)/Chiral Carboxylic Acid Catalyzed Enantioselective C(sp3)–H Alkylation of 8-Ethylquinolines with α,β-Unsaturated Carbonyl Compounds
Iridium(III) Catalysts with an Amide‐Pendant Cyclopentadienyl Ligand: Double Aromatic Homologation Reactions of Benzamides by Fourfold C−H Activation
Allyl 4-Chlorophenyl Sulfone as a Versatile 1,1-Synthon for Sequential α-Alkylation/Cobalt-Catalyzed Allylic Substitution
Catalytic Enantioselective Methylene C(sp 3 )−H Amidation of 8‐Alkylquinolines Using a Cp*Rh III /Chiral Carboxylic Acid System
Imidate as the Intact Directing Group for the Cobalt-Catalyzed C–H Allylation
Chiral 2-Aryl Ferrocene Carboxylic Acids for the Catalytic Asymmetric C(sp3)–H Activation of Thioamides
Cobalt‐Catalyzed Allylic Alkylation Enabled by Organophotoredox Catalysis
Synthesis of Heteroaryl Iodanes(III) viaipso‐Substitution Reactions Using Iodine Triacetate Assisted by HFIP
Enantioselective C(sp 3 )–H Amidation of Thioamides Catalyzed by a Cobalt III /Chiral Carboxylic Acid Hybrid System
Synthesis of Functionalized Monoaryl-λ3 -iodanes through Chemo- and Site-Selective ipso -Substitution Reactions
Chiral Carboxylic Acid Enabled Achiral Rhodium(III)-Catalyzed Enantioselective C−H Functionalization
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