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Synthesis of 2-substituted 2H-chromenes using potassium vinyltrifluoroborates

  • Albert Einstein College of Medicine

Research output: Contribution to journalArticlepeer-review

53 Scopus citations

Abstract

2H-Chromenes were synthesized from salicylaldehyde using potassium vinylic borates in the presence of secondary amines. We synthesized these 2H-chromene derivatives as a part of an ongoing project to develop inhibitors for TGF-β receptors. Potassium vinyl trifluoroborates react with salicylaldehydes at 80 °C in the presence of a secondary amine and produced 2-substituted 2H-chromene derivatives with a 70-90% yield.

Original languageEnglish
Pages (from-to)1578-1581
Number of pages4
JournalTetrahedron Letters
Volume49
Issue number10
DOIs
StatePublished - Mar 3 2008

Keywords

  • Chromenes
  • Potassium organic trifluoroborate
  • Signal transduction
  • TGF-β inhibitors

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