Please use this identifier to cite or link to this item: https://doi.org/10.1039/c3cc45369c
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dc.titleAsymmetric synthesis of 3-spirocyclopropyl-2-oxindoles via intramolecular trapping of chiral aza-ortho-xylylene
dc.contributor.authorDou, X.
dc.contributor.authorYao, W.
dc.contributor.authorZhou, B.
dc.contributor.authorLu, Y.
dc.date.accessioned2014-06-23T05:32:41Z
dc.date.available2014-06-23T05:32:41Z
dc.date.issued2013-10-14
dc.identifier.citationDou, X., Yao, W., Zhou, B., Lu, Y. (2013-10-14). Asymmetric synthesis of 3-spirocyclopropyl-2-oxindoles via intramolecular trapping of chiral aza-ortho-xylylene. Chemical Communications 49 (80) : 9224-9226. ScholarBank@NUS Repository. https://doi.org/10.1039/c3cc45369c
dc.identifier.issn13597345
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75628
dc.description.abstractChiral aza-ortho-xylylene intermediates were efficiently generated from 3-chloro-3-substituted oxindole precursors. The first intramolecular trapping of chiral aza-ortho-xylylene intermediates led to a highly asymmetric synthesis of 3-spirocyclopropyl-2-oxindoles. © 2013 The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c3cc45369c
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c3cc45369c
dc.description.sourcetitleChemical Communications
dc.description.volume49
dc.description.issue80
dc.description.page9224-9226
dc.description.codenCHCOF
dc.identifier.isiut000324490200048
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