• myGriffith
    • Staff portal
    • Contact Us⌄
      • Future student enquiries 1800 677 728
      • Current student enquiries 1800 154 055
      • International enquiries +61 7 3735 6425
      • General enquiries 07 3735 7111
      • Online enquiries
      • Staff phonebook
    View Item 
    •   Home
    • Griffith Research Online
    • Journal articles
    • View Item
    • Home
    • Griffith Research Online
    • Journal articles
    • View Item
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Browse

  • All of Griffith Research Online
    • Communities & Collections
    • Authors
    • By Issue Date
    • Titles
  • This Collection
    • Authors
    • By Issue Date
    • Titles
  • Statistics

  • Most Popular Items
  • Statistics by Country
  • Most Popular Authors
  • Support

  • Contact us
  • FAQs
  • Admin login

  • Login
  • Dialkyl Imidazolium Benzoates – Room Temperature Ionic Liquids Useful in the Peracetylation and Perbenzoylation of Simple and Sulfated Saccharides

    Author(s)
    Murugesan, Saravanababu
    Karst, Nathalie
    Islam, Tasneem
    M. Wiencek, John
    J. Linhardt, Robert
    Griffith University Author(s)
    Islam, Tasneem
    Year published
    2003
    Metadata
    Show full item record
    Abstract
    Dialkyl imidazolium benzoates, room temp. ionic liqs. including 1-ethyl-3-Me imidazolium benzoate, 1-butyl-3-Me imidazolium benzoate and 1-hexyl-3-Me imidazolium benzoate were used in the peracetylation and perbenzoylation of several simple and sulfated carbohydrates. Org. solvents and catalysts were not required in the syntheses and these ionic liqs. gave excellent yields in short reaction times.Dialkyl imidazolium benzoates, room temp. ionic liqs. including 1-ethyl-3-Me imidazolium benzoate, 1-butyl-3-Me imidazolium benzoate and 1-hexyl-3-Me imidazolium benzoate were used in the peracetylation and perbenzoylation of several simple and sulfated carbohydrates. Org. solvents and catalysts were not required in the syntheses and these ionic liqs. gave excellent yields in short reaction times.
    View less >
    Journal Title
    Synlett
    Volume
    2003
    Issue
    9
    Publisher URI
    http://www.thieme-chemistry.com/thieme-chemistry/journals/info/synlett/index.shtml
    Subject
    Medicinal and Biomolecular Chemistry
    Organic Chemistry
    Publication URI
    http://hdl.handle.net/10072/32445
    Collection
    • Journal articles

    Footer

    Disclaimer

    • Privacy policy
    • Copyright matters
    • CRICOS Provider - 00233E

    Tagline

    • Gold Coast
    • Logan
    • Brisbane - Queensland, Australia
    First Peoples of Australia
    • Aboriginal
    • Torres Strait Islander