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Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol301962e
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dc.titleAsymmetric allylic alkylation of isatin-derived Morita-Baylis-Hillman carbonates with nitroalkanes
dc.contributor.authorChen, G.-Y.
dc.contributor.authorZhong, F.
dc.contributor.authorLu, Y.
dc.date.accessioned2014-06-23T05:32:31Z
dc.date.available2014-06-23T05:32:31Z
dc.date.issued2012-08-03
dc.identifier.citationChen, G.-Y., Zhong, F., Lu, Y. (2012-08-03). Asymmetric allylic alkylation of isatin-derived Morita-Baylis-Hillman carbonates with nitroalkanes. Organic Letters 14 (15) : 3955-3957. ScholarBank@NUS Repository. https://doi.org/10.1021/ol301962e
dc.identifier.issn15237060
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75614
dc.description.abstractA stereoselective allylic alkylation of isatin-derived Morita-Baylis- Hillman (MBH) carbonates with nitroalkanes has been developed. In the presence of 10 mol % β-isocupreidine (β-ICD), 3,3′-disubstituted oxindoles were prepared with moderate diastereoselectivities and excellent enantioselectivities. © 2012 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol301962e
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ol301962e
dc.description.sourcetitleOrganic Letters
dc.description.volume14
dc.description.issue15
dc.description.page3955-3957
dc.description.codenORLEF
dc.identifier.isiut000307041600037
Appears in Collections:Staff Publications

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