An enantioselective synthesis of 2-alkyl-3-phenyltropanes by an asymmetric 1,3-dipolar cycloaddition reaction

Gian Luca Araldi, K. R.C. Prakash, Clifford George, Alan P. Kozikowski

Research output: Contribution to journalArticle

Abstract

A method for gaining access to 2-alkyl-3-phenyl-substituted tropanes using the chiral dipolarophile (R)-p-tolyl vinyl sulfoxide in the asymmetric 1,3-dipolar cycloaddition reaction with the oxidopyridinium betaine 4 is described.

Original languageEnglish (US)
Pages (from-to)1875-1876
Number of pages2
JournalChemical Communications
Issue number19
StatePublished - Dec 1 1997

ASJC Scopus subject areas

  • Catalysis
  • Electronic, Optical and Magnetic Materials
  • Ceramics and Composites
  • Chemistry(all)
  • Surfaces, Coatings and Films
  • Metals and Alloys
  • Materials Chemistry

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    Araldi, G. L., Prakash, K. R. C., George, C., & Kozikowski, A. P. (1997). An enantioselective synthesis of 2-alkyl-3-phenyltropanes by an asymmetric 1,3-dipolar cycloaddition reaction. Chemical Communications, (19), 1875-1876.