Sulfur extrusion from 1,4-benzothiazepines: Formation of 3-aryl-4-carbomethoxyisoquinolines

Lajos Fodor, David B. MacLean

Research output: Article

18 Citations (Scopus)


Treatment of 3-aryl-2-carbomethoxy-4,5-dihydro-1 ,4-benzothiazepines with N-chlorosuccinimide in ether gave 3-aryl-4- carbomethoxyisoquinolines in a reaction in which the sulfur atom was extruded from the seven-membered thiazepin ring.

Original languageEnglish
Pages (from-to)18-20
Number of pages3
JournalCanadian Journal of Chemistry
Issue number1
Publication statusPublished - jan. 1 1987

ASJC Scopus subject areas

  • Catalysis
  • Chemistry(all)
  • Organic Chemistry

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