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dc.contributor.authorHanania, Michel
dc.contributor.authorNovak, Lajos
dc.contributor.authorKovacs, Peter
dc.contributor.authorKolonits, Pal
dc.contributor.authorFekete, Jeno
dc.contributor.authorSzabo, Eva
dc.contributor.authorSzantay, Csaba
dc.date.accessioned2018-12-03T10:29:17Z
dc.date.available2018-12-03T10:29:17Z
dc.date.issued1997
dc.identifier.issn0039-7881
dc.identifier.urihttp://dspace.bethlehem.edu:8080/xmlui/handle/123456789/92
dc.description--en_US
dc.description.abstractCycloalkenobenzofurans are prepared in one operation from hydroquinone and cycloakenediol involving a sequence of acid-catalyzed formation of ether , 1,3- and 3,3-rearrangements, and acid-catalyzed intramolecular cyclization of intermediates generated.en_US
dc.description.sponsorship--en_US
dc.language.isoenen_US
dc.publisherThiemeen_US
dc.relation.ispartofseriesSynthesis;8, 909-916
dc.subjectHydroquinones, cycloalkenediols, cycloalkenobenzofurans, rearrangementen_US
dc.titleRearrangement of Allyl Aryl Ethers II, Reactions of Hydroquinones with Cycloalkenediolsen_US
dc.title.alternative--en_US
dc.typeArticleen_US


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