A concise synthesis of 1-substituted-2-tetralones by selective diol dehydration leading to ketone transposition1

dc.contributor.authorBruce L. Jensen
dc.contributor.authorSergei V. Slobodzian
dc.date.accessioned2012-11-14T14:37:10Z
dc.date.accessioned2025-02-17T14:01:15Z
dc.date.available2012-11-14T14:37:10Z
dc.date.issued2012-11-14
dc.descriptionDehydration of 1-substituted-1,2-tetralindiols with zinc iodide a orded the corresponding 2-tetralones in excellent yields. This procedure was found to be superior to the more conventional BF3-catalyzed rearrangement of 1-substituted-1,2-epoxytetralins. # 2000 Elsevier Science Ltd. All rights reserveden_US
dc.description.abstractDehydration of 1-substituted-1,2-tetralindiols with zinc iodide a orded the corresponding 2-tetralones in excellent yields. This procedure was found to be superior to the more conventional BF3-catalyzed rearrangement of 1-substituted-1,2-epoxytetralins. # 2000 Elsevier Science Ltd. All rights reserveden_US
dc.identifier.urihttps://dl.ftveti.edu.et/handle/123456789/4091
dc.language.isoenen_US
dc.subjectketones; rearrangements; epoxides; diolsen_US
dc.titleA concise synthesis of 1-substituted-2-tetralones by selective diol dehydration leading to ketone transposition1en_US
dc.typeArticleen_US

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