Synthesis 1997; 1997(8): 909-916
DOI: 10.1055/s-1997-1288
paper
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Rearrangement of Allyl Aryl Ethers II;1 Reaction of Hydroquinone with Cycloalkenediols

Lajos Novák1 , Péter Kovács2 , Pál Kolonits3 , Michel Hanania3 , Jenő Fekete4 , Éva Szabó4 , Csaba Szántay5
  • 1Institute for Organic Chemistry, Technical University, 1111 Budapest, Gellért tér 4, Hungary, Fax +36(1)4633297; E-mail: L-NOVAK@CH.BME.HU
  • 2Central Research Institute of Chemistry, 1525 Budapest, P.O.box 17, Hungary
  • 3Institute for Organic Chemistry, Technical University, 1111 Budapest, Gellért tér 4, Hungary
  • 4Institute for General and Analytical Chemistry, Technical University, 1111 Budapest, Gellért tér 4, Hungary
  • 5Institute for Organic Chemistry, Technical University, 1111 Budapest, Gellért tér 4, Hungary; Central Research Institute of Chemistry, 1525 Budapest, P.O.box 17, Hungary
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
31. Dezember 2000 (online)

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.