"Syn-Effect" in the Base-Induced Isomerization of Vinylic Sulfones to Allylic Sulfones and the Related Various Reactions
スポンサーリンク
概要
- 論文の詳細を見る
“Syn–effect” has been recognized as a major cause of stabilizing the syn–conformation at the transition state of a number of reactions against the steric hindrance. This account deals with the origin of the “syn–effect” on the basis of the stereochemical outcome in the isomerization of vinylic sulfones leading to the formation of allylic sulfones and in the related various reactions. We proposed that a σ→π* interaction between the σ–orbital(s) of the allylic C–H σ–bond(s) (or of the C–H σ–bond(s) at the α–position for carbonyl compounds) and the antibonding orbital (π*) of the C=C double bond (or of the C=O double bond for carbonyl compounds) is the most important and essential factor for the “syn–effect”, though the contribution of a 6π–electron homoaromaticity and/or of a hydrogen bonding cannot be entirely ruled out.
- 社団法人 有機合成化学協会の論文
- 2009-11-01
著者
-
Inomata Katsuhiko
Division Of Material Sciences Graduate School Of Natural Science And Technology Kanazawa University
-
Inomata Katsuhiko
Division of Material Sciences, Graduate School of Natural Science and Technology, Kanazawa University
関連論文
- "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
- "Syn-Effect" in the Desilylation Reaction of γ-Silylated Allylic and Vinylic Sulfones
- 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 Bis(alkoxycarbonylation) Reaction of Terminal Olfins Catalyzed by Palladium in the Presence of Copper(I) Triflate and a Chiral Bioxazoline Ligand
- 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
- An Efficient Method for the Conversion of 2-Bromo-5-tosylpyrroles to the Corresponding 5-Tosylpyrrolinones as the D-Ring of Phycocyanobilin Derivatives
- "Syn-Effect" in the Desulfonylation Reaction of a, a-Dialkylated (E)-Allylic Sulfones
- "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
- 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
- Selective Transformation of N-(Propargylic)hydroxylamines into 4-Isoxazolines and Acylaziridines Promoted by Metal Salts
- Total Synthesis of Doubly Locked 5Za15Ea-Biliverdin Derivative : A Convergent Synthesis of the E-anti Dipyrrole Component Locked with a 7-Membered Ring
- Studies on the Structure and Function of Phytochromes as Photoreceptors Based on Synthetic Organic Chemistry
- Strecker-Type Reaction of Nitrones Using Cyanohydrin
- Asymmetric Bis(alkoxycarbonylation) Reaction of Cyclic Olefins Catalyzed by Palladium in the Presence of Copper(I) Triflate