• Title of article

    En route to sugar–alkaloid conjugates Original Research Article

  • Author/Authors

    Carsten-Endres Sowa، نويسنده , , Joachim Thiem، نويسنده ,

  • Issue Information
    دوهفته نامه با شماره پیاپی سال 2011
  • Pages
    5
  • From page
    1546
  • To page
    1550
  • Abstract
    After stereoselective addition of N-iodosuccinimide to glycals subsequent dehalogenation results in formation of N-glycopyranosyl succinimides. By UV irradiation both azepindiones and preferentially [5.3.1.02,6] tricyclic oxalactams could be obtained. Their transformation into a number of novel sugar conjugates resembling some prominent alkaloid N-pyrrol components by thiation and reduction is reported.
  • Keywords
    Simplexin oxa-analogs , Glycopyranosyl-N-pyrrol , N-2-Deoxyglycopyranosyl succinimides , 2 , 6] Oxalactams
  • Journal title
    Carbohydrate Research
  • Serial Year
    2011
  • Journal title
    Carbohydrate Research
  • Record number

    967217

    • Link To Document
    https://search.isc.ac/dl/search/defaultta.aspx?DTC=10&DC=967217