Catalytic enantioselective 1,3-dipolar cycloaddition reaction of azomethine ylides and alkenes: the direct strategy to prepare enantioenriched highly substituted proline derivatives

Angew Chem Int Ed Engl. 2005 Oct 7;44(39):6272-6. doi: 10.1002/anie.200501074.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkenes / chemical synthesis*
  • Alkenes / chemistry
  • Azo Compounds / chemical synthesis*
  • Azo Compounds / chemistry
  • Catalysis
  • Cyclization
  • Imines / chemistry
  • Molecular Conformation
  • Proline / analogs & derivatives*
  • Proline / chemical synthesis*
  • Proline / chemistry
  • Pyrrolidines / chemical synthesis
  • Pyrrolidines / chemistry
  • Stereoisomerism
  • Thiosemicarbazones / chemical synthesis*
  • Thiosemicarbazones / chemistry

Substances

  • Alkenes
  • Azo Compounds
  • Imines
  • Pyrrolidines
  • Thiosemicarbazones
  • azomethine
  • Proline