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