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Triflic acid

  • Synergistic Effect of Acids and HFIP on Friedel-Crafts Reactions of Alcohols and Cyclopropanes Vuk Vukovic

    Synergistic Effect of Acids and HFIP on Friedel-Crafts Reactions of Alcohols and Cyclopropanes Vuk Vukovic

  • WO 2015/014733 Al 5 February 2015 (05.02.2015) P O P C T

    WO 2015/014733 Al 5 February 2015 (05.02.2015) P O P C T

  • Copper(II)–Acid Co-Catalyzed Intermolecular Substitution of Electron-Rich Aromatics with Diazoesters

    Copper(II)–Acid Co-Catalyzed Intermolecular Substitution of Electron-Rich Aromatics with Diazoesters

  • Supplementary Information

    Supplementary Information

  • Trifluoromethanesulfonic Acid As Acylation Catalyst: Special Feature for C- And/Or O-Acylation Reactions

    Trifluoromethanesulfonic Acid As Acylation Catalyst: Special Feature for C- And/Or O-Acylation Reactions

  • One-Step Synthesis, Characterization and Oxidative Desulfurization of 12-Tungstophosphoric Heteropolyanions Immobilized on Amino Functionalized SBA-15

    One-Step Synthesis, Characterization and Oxidative Desulfurization of 12-Tungstophosphoric Heteropolyanions Immobilized on Amino Functionalized SBA-15

  • Fluorine Gas F Is the Most Powerful Oxidizing Agent Known, Reacting

    Fluorine Gas F Is the Most Powerful Oxidizing Agent Known, Reacting

  • Wo 2U11/1U4724 A2

    Wo 2U11/1U4724 A2

  • Appendix a Reports the Determination Regarding Whether Or Not Domestic

    Appendix a Reports the Determination Regarding Whether Or Not Domestic

  • Preparation of O-Pivaloyl Hydroxylamine Triflic Acid

    Preparation of O-Pivaloyl Hydroxylamine Triflic Acid

  • Brønsted-Acid-Catalyzed Exchange in Polyester Dynamic Covalent Networks

    Brønsted-Acid-Catalyzed Exchange in Polyester Dynamic Covalent Networks

  • Group Vibrational Mode Assignments As a Broadly Applicable Tool For

    Group Vibrational Mode Assignments As a Broadly Applicable Tool For

  • Triflamide Anchored SBA-15 Catalyst for Nitration of Alkyl Aromatics in Microwave

    Triflamide Anchored SBA-15 Catalyst for Nitration of Alkyl Aromatics in Microwave

  • (12) Patent Application Publication (10) Pub. No.: US 2008/0021235 A1 Lebedev (43) Pub

    (12) Patent Application Publication (10) Pub. No.: US 2008/0021235 A1 Lebedev (43) Pub

  • Robert H. Morris

    Robert H. Morris

  • Acidity and Reactivity of Trifluoromethanesulfonic Acid in Liquid and Solid Acid Catalysts

    Acidity and Reactivity of Trifluoromethanesulfonic Acid in Liquid and Solid Acid Catalysts

  • Common Acid and Base Storage Group Recommendations

    Common Acid and Base Storage Group Recommendations

  • Trifluoromethanesulfonic Acid As Acylation Catalyst

    Trifluoromethanesulfonic Acid As Acylation Catalyst

Top View
  • Incompatible Chemicals
  • About the Acidity-Catalytic Activity Relationship in Ionic Liquids: Application to the Selective Isobutene Dimerization
  • PRODUCT LIST Industrial
  • Protonation and Other Acid-Base Chemistry Of
  • Carborane Acids. New ‘‘Strong Yet Gentle’’ Acids for Organic and Inorganic Chemistry
  • 1 Protonolysis of Fe-C Bonds of a Diiminopyridineiron(II) Dialkyl Complex by Acids of Different Strengths: Influence of Monoanio
  • Working with Hazardous Chemicals
  • Recent Evidence for the Association of Initiator with Counter Ion in Cationic Polymerization
  • “Superacids” Safety Guidelines
  • Public Law 115–239 115Th Congress an Act to Amend the Harmonized Tariff Schedule of the United States to Modify Temporarily Sept
  • Trifluoromethanesulfonic Acid
  • Nitronium Salts in Superacidic and Aprotic Media: Activation of the Nitronium Ion by Protosolvation GEORGE A
  • Keteniminium Ions: Unique and Versatile Reactive Intermediates for Chemical Synthesis
  • Aldrichimica Acta 48.3
  • APPLIED CHEMISTRY Effects of Solvent Acidity on the Free-Radical
  • A Strong Acid That Does Not Protonate Water
  • United States Patent (19) 11 Patent Number: 4,598,131 Prucnal 45 Date of Patent: Jul
  • Ionization Constants of Aqueous Amino Acids at Temperatures up to 250°C Using Hydrothermal Ph Indicators and UV-Visible Spectroscopy: Glycine, ␣-Alanine, and Proline


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