• Title of article

    Unexpected epimerization and stereochemistry revision of IMDA adducts from sorbate-related 1,3,8-nonatrienes

  • Author/Authors

    Wu، نويسنده , , Jinlong and Yu، نويسنده , , Haihua and Wang، نويسنده , , Yan-yan Xing، نويسنده , , Xinglong and Dai، نويسنده , , Wei-Min، نويسنده ,

  • Issue Information
    هفته نامه با شماره پیاپی سال 2007
  • Pages
    5
  • From page
    6543
  • To page
    6547
  • Abstract
    Intramolecular Diels–Alder (IMDA) reaction of two sorbate-related 1,3,8-nonatrienes has been investigated in MeCN at 180 °C for 1.5 h under controlled microwave heating. On checking the crude product mixture before purification, partial epimerization of the major adduct was found during the reaction. After column chromatographic purification over silica gel, only two cis adducts were obtained and their structures have been thoroughly established by X-ray crystallographic analysis. It is concluded that the putative major trans adduct predicted by the IMDA reaction mechanism undergoes facile epimerization at high temperature or in the presence of silica gel. Structural revision on the adducts has been made.
  • Keywords
    intramolecular Diels–Alder reaction , Isomerization , microwave , Stereochemistry , Sorbate , lactone
  • Journal title
    Tetrahedron Letters
  • Serial Year
    2007
  • Journal title
    Tetrahedron Letters
  • Record number

    1856432