Inomata Katsuhiko | Division of Material Sciences, Graduate School of Natural Science and Technology, Kanazawa University

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著作論文

"Syn-Effect" in the Conversion of (E)-α, β-Unsaturated Esters into the Corresponding β, γ-Unsaturated Esters and Aldehydes into Silyl Enol Ethers
"Syn-Effect" in the Conversion of (E)-α, β-Unsaturated Esters to the Corresponding β, γ-Unsaturated Esters
"Syn-Effect"in the Isomerization of (E)-α-Fluorovinylic Sulfones to the Corresponding Allylic Sulfones under Basic Conditions
Ring-opening Bis(alkoxycarbonylation) Reaction of Methylenecyclopropanes Catalyzed by Palladium in the Presence of Copper(I) Salt
Asymmetric Bis(alkoxycarbonylation) Reaction of Cyclic Olefins Catalyzed by Palladium in the Presence of Copper(I) Triflate
Asymmetric Addition of Alkynylzinc Reagents to Nitrones Utilizing Tartaric Acid Ester as a Chiral Auxiliary
Total Syntheses of Doubly Locked Biliverdin Derivatives toward Elucidation of the Stereochemistry of Phytochrome Chromophore
Syntheses of Biliverdin Derivatives Sterically Locked at the CD-Ring Components
Synthesis of Biliverdin Derivative Bearing the Sterically Fixed E-anti C/D-Ring Component
Synthesis of the Sterically Fixed Biliverdin Derivative Bearing the Z-anti C/D-Ring Component
Regioselective Oxidation of Pyrrole Derivatives with DDQ and Its Synthetic Application
Asymmetric 1,3-Dipolar Cycloaddition of Nitrones with an Electron-Withdrawing Group to Allylic Alcohols Utilizing Diisopropyl Tartrate as a Chiral Auxiliary
Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Imines to Homoallytic Alcohols
Asymmetric 1,3-Dipolar Cycloaddition Reaction of Azomethine Imines to Allyl Alcohol
Catalytic Asymmetric Addition of Alkynylzinc Reagents to Nitrones
The First Enantioselective Hetero Diels-Alder Reaction of Nitroso Compound Utilizing Tartaric Acid Ester as a Chiral Auxiliary
Catalytic Asymmetric 1,3-Dipolar Cycloaddition of a Nitrone Bearing a Bulky Amide Moiety to γ-Substituted Allylic Alcohols
Synthesis of Doubly Locked 5Zs15Za-Biliverdin Derivatives and Their Unique Spectral Behavior
Total Syntheses of Sterically Locked Phycocyanobilin Derivatives Bearing a 15Z-anti or a 15E-anti CD-Ring Component
Stereoselective One-pot 1,4-Elimination and the [1,2]-Wittig Rearrangement of (E)-δ-(Arylmethoxy or 3-Silyl-2-propynyloxy)-substituted Allylic Sulfones
"Syn-Effect" in the Base-Induced Isomerization of Vinylic Sulfones to Allylic Sulfones and the Related Various Reactions
Total Synthesis of Doubly Locked 5Za15Ea-Biliverdin Derivative : A Convergent Synthesis of the E-anti Dipyrrole Component Locked with a 7-Membered Ring
Strecker-Type Reaction of Nitrones Using Cyanohydrin

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