Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol006918c
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dc.titleSynthetic studies toward anisatin: A formal synthesis of (±)-8-deoxyanisatin
dc.contributor.authorLoh, T.-P.
dc.contributor.authorHu, Q.-Y.
dc.date.accessioned2014-10-16T08:44:49Z
dc.date.available2014-10-16T08:44:49Z
dc.date.issued2001-01-25
dc.identifier.citationLoh, T.-P., Hu, Q.-Y. (2001-01-25). Synthetic studies toward anisatin: A formal synthesis of (±)-8-deoxyanisatin. Organic Letters 3 (2) : 279-281. ScholarBank@NUS Repository. https://doi.org/10.1021/ol006918c
dc.identifier.issn15237060
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/95184
dc.description.abstractequations presented An efficient strategy to construct the congested C-7a quaternary chiral center of anisatin was developed, by way of an Eschenmoser-Claisen rearrangement. Conversion of the resultant amide to Kende's ε-lactone intermediate 3 in four steps completed a concise formal synthesis of (±)-8-deoxyanisatin (2).
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol006918c
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ol006918c
dc.description.sourcetitleOrganic Letters
dc.description.volume3
dc.description.issue2
dc.description.page279-281
dc.identifier.isiut000166529300035
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