Short and efficient method for the preparation of furo[3,2-f] quinoline

Mercedesz Törincsi, P. Kolonits, Endre Pálosi, Melinda Fekete, L. Novák

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Furo[3,2-f]quinolines 5 were prepared by reacting the sodium salt of quinolin-6-ol and allyl bromides 2. The allyl aryl ethers 3 formed were then thermally rearranged under standard or microwave conditions. Acid-catalyzed cyclization of the products 4 afforded the title compounds.

Original languageEnglish
Pages (from-to)43-53
Number of pages11
JournalArkivoc
Volume2008
Issue number3
Publication statusPublished - 2008

Fingerprint

Quinolines
Ethers
Cyclization
Salts
Sodium
Microwaves
Acids
quinoline
6-hydroxyquinoline
allyl bromide

Keywords

  • Allyl aryl ethers
  • Claisen rearrangement
  • Furo[3,2-f]quinoline
  • Pyrano[3,2-f]quinoline
  • Ring closure
  • Sonochemical conditions

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Short and efficient method for the preparation of furo[3,2-f] quinoline. / Törincsi, Mercedesz; Kolonits, P.; Pálosi, Endre; Fekete, Melinda; Novák, L.

In: Arkivoc, Vol. 2008, No. 3, 2008, p. 43-53.

Research output: Contribution to journalArticle

Törincsi, M, Kolonits, P, Pálosi, E, Fekete, M & Novák, L 2008, 'Short and efficient method for the preparation of furo[3,2-f] quinoline', Arkivoc, vol. 2008, no. 3, pp. 43-53.
Törincsi, Mercedesz ; Kolonits, P. ; Pálosi, Endre ; Fekete, Melinda ; Novák, L. / Short and efficient method for the preparation of furo[3,2-f] quinoline. In: Arkivoc. 2008 ; Vol. 2008, No. 3. pp. 43-53.
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