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Triflate

  • Optimizing the Least Nucleophilic Anion. a New, Strong Methyl+ Reagent Daniel Stasko and Christopher A

    Optimizing the Least Nucleophilic Anion. a New, Strong Methyl+ Reagent Daniel Stasko and Christopher A

  • Aldol Reactions: E-Enolates and Anti-Selectivity

    Aldol Reactions: E-Enolates and Anti-Selectivity

  • Probing Ion Exchange in the Triflic Acid-Guanidinium Triflate System: a Solid- State Nuclear Magnetic Resonance Study

    Probing Ion Exchange in the Triflic Acid-Guanidinium Triflate System: a Solid- State Nuclear Magnetic Resonance Study

  • (And In-Betweens) of Solubility Measurements of Solid Electrolytes*

    (And In-Betweens) of Solubility Measurements of Solid Electrolytes*

  • Catalytic Silane Nanopatterning Using Scandium Triflate Functionalised PPL Arrays

    Catalytic Silane Nanopatterning Using Scandium Triflate Functionalised PPL Arrays

  • Formal Synthesis of (+/-) Morphine Via an Oxy-Cope/Claisen/Ene Reaction Cascade

    Formal Synthesis of (+/-) Morphine Via an Oxy-Cope/Claisen/Ene Reaction Cascade

  • Functional Group Interconversions 119

    Functional Group Interconversions 119

  • Synthesis of Lycodine-Type Lycopodium Alkaloids Using C-H Functionalization Tactics by James Neel Newton a Dissertation Submitte

    Synthesis of Lycodine-Type Lycopodium Alkaloids Using C-H Functionalization Tactics by James Neel Newton a Dissertation Submitte

  • Synthesis of (+)-Lineariifolianone and Related Cyclopropenone- Containing Sesquiterpenoids Keith P

    Synthesis of (+)-Lineariifolianone and Related Cyclopropenone- Containing Sesquiterpenoids Keith P

  • A Convenient Synthesis of Triflate Anion Ionic Liquids and Their Properties

    A Convenient Synthesis of Triflate Anion Ionic Liquids and Their Properties

  • Enolate Chemistry

    Enolate Chemistry

  • Boron Enolate of Tert-Butyl Methyl Ketone

    Boron Enolate of Tert-Butyl Methyl Ketone

  • Attempted Azidation of Carbohydrate Secondary Alcohols Using Arylsulfonyl Azides

    Attempted Azidation of Carbohydrate Secondary Alcohols Using Arylsulfonyl Azides

  • Sc(Otf)3 Catalyzed Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions: a Review

    Sc(Otf)3 Catalyzed Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions: a Review

  • Diaryliodonium Salts Development of Synthetic Methodologies and Α-Arylation of Enolates

    Diaryliodonium Salts Development of Synthetic Methodologies and Α-Arylation of Enolates

  • ICH M7 – Regulatory Updates & Industry Practices

    ICH M7 – Regulatory Updates & Industry Practices

  • Attempted Total Syntheses of a Novel Lycopodine-Class Alkaloid and (R)-Myricanol, Compounds for the Treatment of Alzheimer's D

    Attempted Total Syntheses of a Novel Lycopodine-Class Alkaloid and (R)-Myricanol, Compounds for the Treatment of Alzheimer's D

  • Aluminium Triflate-Mediated Organic Synthesis

    Aluminium Triflate-Mediated Organic Synthesis

Top View
  • 10.3 Sulfonate and Inorganic Ester Derivatives of Alcohols 443
  • The Total Synthesis of Natural Products Possessing Biological Activity in Two Important Areas
  • Bismuth(III) Triflate Catalyzed Allylation of Cyclic Acetals
  • Contribution to the Chemistry of Boron, 136 [1] a Reinvestigation of the Existence of L,3,2-Dioxaborinium(L-|-) Cations
  • Galanthamine
  • 23Na NMR Mobility Studies on New Electrolytes for Sodium-Ion Batteries
  • Total Asymmetric Synthesis of Ring-A Derivatives of (+)-Trans-Dihydronarciclasine
  • Metal Triflates
  • Triflate Catalyzed Efficient Strecker Reaction of Ketones and Their Fluorinated Analogs
  • Triflate and Related Low Oxidation State Indium Salts
  • Working with Hazardous Chemicals
  • New Stereoselective Reactions to Form Amido Alkyl C-N and Vinyl Triflate C-O
  • A Strong Acid That Does Not Protonate Water
  • Development of New Reactions Employing Boron-Enolate Wittig Rearrangements
  • Comparing Triflate and Hexafluorophosphate Anions of Ionic Liquids in Polymer Electrolytes for Supercapacitor Applications
  • Methyl Triflate
  • Sodium Trifluoromethanesulfonate Safety Data Sheet 6164223 According to Federal Register / Vol
  • Activation of Alcohols to Nucleophilic Substitution


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