Palladium-Catalyzed Carbonylation of Homoallylic Amine Derivatives in the Presence of a Copper Co-catalyst

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概要

• 論文の詳細を見る
• Chemical Society of Japanの論文
• 2003-06-15

著者

• Ukaji Yutaka

  Department Of Chemical Science Graduate School Of Natural Science And Technology Kanazawa University

• Inomata Katsuhiko

  Department Of Chemical Science Graduate School Of Natural Science And Technology Kanazawa University

• MIZUTANI Takanori

  Department of Chemical Science, Graduate School of Natural Science and Technology, Kanazawa Universi

• Mizutani T

  Department Of Chemical Science Graduate School Of Natural Science And Technology Kanazawa University

関連論文

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• "Syn-Effect"in the Isomerization of (E)-α-Fluorovinylic Sulfones to the Corresponding Allylic Sulfones under Basic Conditions
• "Syn-Effect" in the Desilylation Reaction of γ-Silylated Allylic and Vinylic Sulfones
• Asymmetric Bis(alkoxycarbonylation) Reaction of Terminal Olfins Catalyzed by Palladium in the Presence of Copper(I) Triflate and a Chiral Bioxazoline Ligand
• Asymmetric Bis(alkoxycarbonylation) Reaction of Homoallylic Alcohols Catalyzed by Palladium in the Presence of Cu(I) Triflate Using the Chiral Bioxazoline Ligand
• An Efficient Method for the Conversion of 2-Bromo-5-tosylpyrroles to the Corresponding 5-Tosylpyrrolinones as the D-Ring of Phycocyanobilin Derivatives
• Total Syntheses of Phycocyanobilin Derivatives Bearing a Modified A-Ring toward the Structure/Function Analysis of Phytochrome
• Efficient Synthesis of B- and C-Rings Components of Phycobilin Derivatives for Structure/Function Analysis of Phytochrome
• 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
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• 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
• Asymmetric Addition of Reformatsky-Type Reagent to Imines Utilizing Diisopropyl Tartrate as a Chiral Auxiliary
• Efficient Construction of A, B-Rings Component for Syntheses of Phycocyanobilin and Its Derivative
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• Rearrangement of Tosyl Group of 3,4-Disubstituted 2-Tosylpyrroles under Mild Acidic Conditions
• A Highly Efficient Method for the Preparation of the A/B-Ring Component of Phycobilin Derivatives Starting from Bilirubin
• Palladium-Catalyzed Carbonylation of Homoallylic Amine Derivatives in the Presence of a Copper Co-catalyst
• Asymmetric 1,3-Dipolar Cycloaddition of Nitrile Oxides Generated in situ by Direct Oxidation of Aldoximes
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• Enantioselective Synthesis of 2-Isoxazolines via Asymmetric 1,3-Dipolar Cycloaddition of Nitrile Oxide to Achiral Allyl Alcohol
• Synthesis of Silicon Substituted Cyclopropylmethyl Alcohols in Optically Active Form via Asymmetric Simmons-Smith Reaction of γ-Silicon Substituted Allylic Alcohols
• Enantioselective Construction of Cyclopropane Rings via Asymmetric Simmons-Smith Reaction of Allylic Alcohols
• A general synthetic method for 1-substituted 1,4-dihydro-3(2H)-isoquinolinones.
• The reactions of 2-fluoro-1,3,5-trinitrobenzene (FTNB) as a new condensing reagent.
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• Selective Mono- and Bis(alkoxycarbonylation)s of Olefins Catalyzed by Palladium in the Presence of Cu(I) or Cu(II) Chloride under Remarkably Mild Conditions. Application to the Synthesis of .GAMMA.-Butyrolactone Derivatives.
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• Quaternary ammonium periodate as a new oxidizing agent.
• Selective 1,4-chiral induction in the reaction of enolates generated from t-butyl .DELTA.-hydroxy carboxylates.

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