Please use this identifier to cite or link to this item:
https://doi.org/10.1039/c3cc45369c
DC Field | Value | |
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dc.title | Asymmetric synthesis of 3-spirocyclopropyl-2-oxindoles via intramolecular trapping of chiral aza-ortho-xylylene | |
dc.contributor.author | Dou, X. | |
dc.contributor.author | Yao, W. | |
dc.contributor.author | Zhou, B. | |
dc.contributor.author | Lu, Y. | |
dc.date.accessioned | 2014-06-23T05:32:41Z | |
dc.date.available | 2014-06-23T05:32:41Z | |
dc.date.issued | 2013-10-14 | |
dc.identifier.citation | Dou, 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.issn | 13597345 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/75628 | |
dc.description.abstract | Chiral 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.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c3cc45369c | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.description.doi | 10.1039/c3cc45369c | |
dc.description.sourcetitle | Chemical Communications | |
dc.description.volume | 49 | |
dc.description.issue | 80 | |
dc.description.page | 9224-9226 | |
dc.description.coden | CHCOF | |
dc.identifier.isiut | 000324490200048 | |
Appears in Collections: | Staff Publications |
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