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dc.contributor.authorNovak, Lajos
dc.contributor.authorKovacs, Peter
dc.contributor.authorPirok, Gyorgy
dc.contributor.authorKolonits, Pal
dc.contributor.authorHanania, Michel
dc.contributor.authorDonath, Katalin
dc.contributor.authorSzantay, Csaba
dc.date.accessioned2018-12-03T11:01:35Z
dc.date.available2018-12-03T11:01:35Z
dc.date.issued1997
dc.identifier.issn0040-4020
dc.identifier.urihttp://dspace.bethlehem.edu:8080/xmlui/handle/123456789/94
dc.description--en_US
dc.description.abstractCycloalkenobenzofurans were prepared in one-pot reaction from methoxyhydroquinone, 2,5- and 2,6 and 2,3- dialkoxyhydroquinone with cycloalkenediol. Reaction between isomeric 2,5- dialkoxyhydroquinone with diol led to the formation of monoalkoxybenzofurans with the loss of an alkoxy group.en_US
dc.description.sponsorship--en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofseriesTetrahedron;53 (28), 9789-9798
dc.subjectAlkoxyhydroquinones, cycloalkenediols, cycloalkenobenzofurans, rearrangementen_US
dc.titleRearrangement of Allyl Aryl Ethers III, Reactions of Alkoxyhydroquinones with Cycloalkenediolsen_US
dc.title.alternative--en_US
dc.typeArticleen_US


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