Rearrangement of allyl aryl ethers II; Reaction of hydroquinone with a cycloalkenediols

L. Novák, Péter Kovács, P. Kolonits, Michel Hanania, J. Fekete, Éva Szabó, Csaba Szántay

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Cycloalkenobenzofurans 5 and 7 are prepared in one operation from hydroquinone 1 and cycloalkenediol 2 involving a sequence of acid-catalyzed formation of ether 3, 1,3- and/or 3,3-rearrangements, and acid-catalyzed intramolecular cyclization of 4 and 6 generated as intermediates.

Original languageEnglish
Pages (from-to)909-916
Number of pages8
JournalSynthesis
Issue number8
Publication statusPublished - 1997

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Ethers
Acids
Cyclization
Ether
hydroquinone

ASJC Scopus subject areas

  • Organic Chemistry

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Rearrangement of allyl aryl ethers II; Reaction of hydroquinone with a cycloalkenediols. / Novák, L.; Kovács, Péter; Kolonits, P.; Hanania, Michel; Fekete, J.; Szabó, Éva; Szántay, Csaba.

In: Synthesis, No. 8, 1997, p. 909-916.

Research output: Contribution to journalArticle

Novák, L. ; Kovács, Péter ; Kolonits, P. ; Hanania, Michel ; Fekete, J. ; Szabó, Éva ; Szántay, Csaba. / Rearrangement of allyl aryl ethers II; Reaction of hydroquinone with a cycloalkenediols. In: Synthesis. 1997 ; No. 8. pp. 909-916.
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