Synthesis of trans,trans-2,3,4-trisubstituted chromans from 3-nitro-2De-chromenes and enamines of acetoacetic ester and acetylacetone. A new type of configurationally stable atropisomers

Research output: Contribution to journalArticle

6 Citations (Scopus)
Original languageEnglish
Pages (from-to)531-540
Number of pages10
JournalChemistry of Heterocyclic Compounds
Volume51
Issue number6
DOIs
Publication statusPublished - Jun 2015

Keywords

  • chromans
  • 3-nitro-2H-chromenes
  • push-pull enamines
  • atropisomerism
  • nucleophilic addition
  • POTASSIUM CHANNEL ACTIVATORS
  • ANTIHYPERTENSIVE ACTIVITY
  • STEREOSELECTIVE ADDITION
  • MICHAEL ADDITION
  • N-NUCLEOPHILES
  • C-NUCLEOPHILES
  • S-NUCLEOPHILES
  • 3-NITRO-2-TRIHALOMETHYL-2H-CHROMENES
  • 3-NITRO-2H-CHROMENES
  • ISOMERS

ASJC Scopus subject areas

  • Organic Chemistry

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