Okuyama Tadashi | Graduate School Of Material Sci. Himeji Inst. Of Technol. Univ. Of Hyogo Kohto Kamigori Hyogo 678-12

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著作論文

Reactions of 2,2-Dialkylvinyl Iodonium Salt with Halide Ions
Solvolysis of 2, 2-Dialkylvinyl Iodonium Salt : Alkyl Participation and Possibility of a Primary Vinylic Cation Intermediate
Solvolysis of β,β-Dialkylvinyliodonium Salt : Primary Vinyl Cation Intermediate and Alkyl Participation
Vinylic S_N2 Reaction of 1-Decenyliodonium Salt with Halide Ions
Ligand Coupling Mechanism of Nucleophilic Vinylic Substitution of Iodonium Salts with Hypervalent 10-I-3 and 12-I-4 Intermediates
Preparation of Methoxy-Substituted Optically Active 7-Alkoxycarbonylcycloheptatrienes and Their Acid-Promoted Rearrangements
Perhydroxylation of Chiral Cycloheptatriene Ring through Stepwise Oxidation under Regio- and Stereocontrol
Regioselective Formation of Optically Active Cycloheptatrienes by Chiral Tethered Buchner Reaction
Novel Acid-Catalyzed Rearrangement of Alkoxycarbonylcycloheptatriene Assisted by Alkoxy Substitution
Carbenoid Addition to Phenols to Give Cycloheptatrienols. Stereochemical Regulation and Ligand-dependent Switching of Chemoselectivity
Stereoselective Intramolecular O-H Insertion of Rhodium Carbenoid Controlled by the 2,4-Pentanediol Tether
Generation of Cycloheptyne during the Solvolysis of Cyclohexylidenemethyliodonium Salt in the Presence of Base
Michael Addition of Cyanide to Cyclohex-1-enyliodonium Salts
Cyclohexynes. Generation from Iodonium Salts and Regioselective Reaction with Nucleophile
Solvolysis of Optically Active 4-Methylcyclohexylidenemethyl Triflate: Evidence against a Primary Vinyl Cation as an Intermediate
Regioselectivity in Nucleophilic Addition of Siloxyalkenes to an Alkylideneallyl Cation
Chirality probe approach to reactive intermediates : Primary vinyl cation and cycloalkyne
Asymmetric Synthesis of gem-Dimethylcyclopropane-fused Compounds through Chemo-, Regio-, and Stereoselective Cyclopropanation and Stereospecific Rearrangement
Temperature-Independent Stereoselectivity in Intramolecular Cycloaddition of Ketene Generated from Diazoester in Solution and in Vapor Phase : How Entropy Term Governs the Selectivity

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