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|Title:||Asymmetric synthesis of 3-spirocyclopropyl-2-oxindoles via intramolecular trapping of chiral aza-ortho-xylylene||Authors:||Dou, X.
|Issue Date:||14-Oct-2013||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||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.||Source Title:||Chemical Communications||URI:||http://scholarbank.nus.edu.sg/handle/10635/75628||ISSN:||13597345||DOI:||10.1039/c3cc45369c|
|Appears in Collections:||Staff Publications|
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