Preparation and cycloaddition chemistry of 1-amino substitutedisobenzofurans

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Abstract

A new strategy for the synthesis of the core skeleton of the benzophenanthridine alkaloid corynoline has been developed which is based on an intramolecular [4+2]-cycloaddition of an amino substituted isobenzofuran derivative.

Original languageEnglish (US)
Pages (from-to)62-76
Number of pages15
JournalArkivoc
Volume2003
Issue number14
Publication statusPublished - Dec 1 2003
Externally publishedYes

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Keywords

  • 1-amino substituted isobenzofuran
  • Cycloaddition
  • Diels-Alder
  • Intramolecular

ASJC Scopus subject areas

  • Organic Chemistry

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