Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol006918c
DC FieldValue
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
Appears in Collections:Staff Publications

Show simple item record
Files in This Item:
There are no files associated with this item.

SCOPUSTM   
Citations

36
checked on Nov 21, 2019

WEB OF SCIENCETM
Citations

30
checked on Nov 21, 2019

Page view(s)

44
checked on Nov 9, 2019

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.