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Department Of Chemistry Faculty Of Science Kanazawa University Kakuma | 論文
- An Efficient Method to Construct the A,B-Rings Component toward Total Syntheses of Phycocyanobilin and Its Derivative as a Photoprobe
- Total Syntheses of (±)-Phycocyanobilin and Its Derivatives Bearing a Photoreactive Group at D-ring
- Syntheses of 3,4-Disubstituted 2-Tosylpyrroles and 5-Tosyl-1,5-dihydro-2H-pyrrol-2-ones Starting from Ethyl 3,4-Disubstituted 2-Pyrrolecarboxylates
- Convenient and Regioselective Syntheses of 3, 4-Disubsutituted Δ^3-Pyrrolin-2-one Derivatives Starting from 2-Tosyl-3, 4-Disubstituted Pyrroles
- Catalytic Asymmetric 1, 3-Dipolar Cycloaddition of Nitrile Oxides to an Achiral Allyl Alcohol Utilizing Diisopropyl Tartrate as a Chiral Auxiliary
- "Syn-Effect" in the Desulfonylation Reaction of a, a-Dialkylated (E)-Allylic Sulfones
- Catalytic Asymmetric Addition of Dialkylzinc to 3,4-Dihydroisoquinoline N-Oxides Utilizing Tartaric Acid Ester as a Chiral Auxiliary
- Catalytic Asymmetric Addition Reaction of Dialkylzinc to Nitrone Utilizing Tartaric Acid Ester as a Chiral Auxiliary
- "Syn Effect" in the 1,4-Eliminative Ring Opening of [3-Substituted (E)-1-Propenyl]oxiranes to the Corresponding 2,4-Dienyl Alcohols
- Palladium-Catalyzed Elimination Reaction of Acyclic (E)-Allylic Acetates : The Stereochemistry Elucidated by "Syn-Effect"
- "Syn Effect" in Nucleophilic Addition of Amines to 1,3-Dienyl Sulfone and Ethyl (E)-2,4-Pentadienoate
- "Syn-Effect" in Nucleophilic Addition of Amines to 1,3-Dienylsulfone
- Pt-B Catalyst Supported on Phosphates for controlling Emissions of NOx, CO and Hydrocarbon at Low Temperatures
- A New Method for the Preparation of A- and D-Rings of Phycocyanobilin Using Mucochloric Acid as a Starting Material
- A New Aerobic Oxidation System Using Pd-Cu Catalysts in the Presence of CO
- A New and Convenient Wittig-type Reaction for the Preparation of Pyrromethenone Derivative
- Catalytic asymmetric 1,3-dipolar cycloaddition of azomethine imines to allyl alcohol utilizing tartaric acid ester as a chiral auxiliary
- 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
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