Please use this identifier to cite or link to this item: https://doi.org/10.1002/anie.201006316
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dc.titleThe direct asymmetric vinylogous aldol reaction of furanones with α-ketoesters: Access to chiral γ-Butenolides and glycerol derivatives
dc.contributor.authorLuo, J.
dc.contributor.authorWang, H.
dc.contributor.authorHan, X.
dc.contributor.authorXu, L.-W.
dc.contributor.authorKwiatkowski, J.
dc.contributor.authorHuang, K.-W.
dc.contributor.authorLu, Y.
dc.date.accessioned2014-10-16T08:45:13Z
dc.date.available2014-10-16T08:45:13Z
dc.date.issued2011-02-18
dc.identifier.citationLuo, J., Wang, H., Han, X., Xu, L.-W., Kwiatkowski, J., Huang, K.-W., Lu, Y. (2011-02-18). The direct asymmetric vinylogous aldol reaction of furanones with α-ketoesters: Access to chiral γ-Butenolides and glycerol derivatives. Angewandte Chemie - International Edition 50 (8) : 1861-1864. ScholarBank@NUS Repository. https://doi.org/10.1002/anie.201006316
dc.identifier.issn14337851
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/95219
dc.description.abstractTwice as good: The title reaction using the tryptophan-derived bifunctional organic catalyst 1 has been developed. The reported method led to the synthesis of chiral γ-substituted butenolides in excellent yields, with high diastereo- and enantioselectivities. Facile synthesis of chiral glycerol derivatives containing a tertiary hydroxy group has also been demonstrated. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/anie.201006316
dc.sourceScopus
dc.subjectaldol reaction
dc.subjectasymmetric synthesis
dc.subjectbutenolides
dc.subjectglycerol derivatives
dc.subjectorganocatalysis
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1002/anie.201006316
dc.description.sourcetitleAngewandte Chemie - International Edition
dc.description.volume50
dc.description.issue8
dc.description.page1861-1864
dc.description.codenACIEA
dc.identifier.isiut000287836200021
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