Synthetic studies toward anisatin: A formal synthesis of (±)-8-deoxyanisatin

Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol006918c

DC Field	Value
dc.title	Synthetic studies toward anisatin: A formal synthesis of (±)-8-deoxyanisatin
dc.contributor.author	Loh, T.-P.
dc.contributor.author	Hu, Q.-Y.
dc.date.accessioned	2014-10-16T08:44:49Z
dc.date.available	2014-10-16T08:44:49Z
dc.date.issued	2001-01-25
dc.identifier.citation	Loh, 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.issn	15237060
dc.identifier.uri	http://scholarbank.nus.edu.sg/handle/10635/95184
dc.description.abstract	equations 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.uri	http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol006918c
dc.source	Scopus
dc.type	Article
dc.contributor.department	CHEMISTRY
dc.description.doi	10.1021/ol006918c
dc.description.sourcetitle	Organic Letters
dc.description.volume	3
dc.description.issue	2
dc.description.page	279-281
dc.identifier.isiut	000166529300035
Appears in Collections:	Staff Publications

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