Please use this identifier to cite or link to this item: https://doi.org/10.1039/c3cc45369c
Title: Asymmetric synthesis of 3-spirocyclopropyl-2-oxindoles via intramolecular trapping of chiral aza-ortho-xylylene
Authors: Dou, X.
Yao, W.
Zhou, B.
Lu, Y. 
Issue Date: 14-Oct-2013
Source: 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
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