Domino constructions of pentacyclic indeno[2,1-c]quinolines and pyrano[4,3-b]oxepines by [4+1]/[3+2+1]/[5+1] and [4+3] multiple cyclizations

Bo Jiang, Bao Ming Feng, Shu Liang Wang, Shu Jiang Tu, Guigen Li

Research output: Contribution to journalArticle

59 Scopus citations

Abstract

New three-component domino reactions have been discovered. The reactions are easy to perform (see scheme; MW=microwave irradiation) and proceed with fast rates, which makes work-up convenient. Most of the multiple stereocenters and the geometry are controlled well. The stereochemistry has been unequivocally determined by X-ray structural analysis.

Original languageEnglish
Pages (from-to)9823-9826
Number of pages4
JournalChemistry - A European Journal
Volume18
Issue number32
DOIs
StatePublished - Aug 6 2012

Keywords

  • domino reactions
  • nitrogen heterocycles
  • pentacyclic indeno[2,1-c]quinoline
  • pyrano[4,3-b]oxepine
  • stereochemistry

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