dc.contributor.authorYang, Caiyun
dc.contributor.authorChen, Wenchao
dc.contributor.authorYang, Wenguo
dc.contributor.authorZhu, Bo
dc.contributor.authorYan, Lin
dc.contributor.authorTan, Choon-Hong
dc.contributor.authorJiang, Zhiyong
dc.date.accessioned2014-03-14T04:08:43Z
dc.date.available2014-03-14T04:08:43Z
dc.date.copyright2013en_US
dc.date.issued2013
dc.identifier.citationYang, C., Chen, W., Yang, W., Zhu, B., Yan, L., Tan, C. H., et al. (2013). Bicyclic-Guanidine-Catalyzed Asymmetric Michael Addition of 3-Substituted Oxindoles to 2-Cyclopentenone. Chemistry - An Asian Journal, 8(12), 2960-2964.en_US
dc.identifier.issn1861-4728en_US
dc.identifier.urihttp://hdl.handle.net/10220/18901
dc.description.abstractTaking the Michael: The first highly enantio- and diastereoselective Michael addition of various 3-benzyl-substituted oxindoles to 2-cyclopentenone has been developed. A variety of 3,3-disubstituted oxindoles as Michael adducts were obtained in 69–99 % yield with 73–98 % ee and 9:1 to >20:1 d.r.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesChemistry - an Asian journalen_US
dc.rights© 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.en_US
dc.subjectDRNTU::Science::Chemistry::Physical chemistry
dc.titleBicyclic-guanidine-catalyzed asymmetric Michael addition of 3-substituted oxindoles to 2-cyclopentenoneen_US
dc.typeJournal Article
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.identifier.doihttp://dx.doi.org/10.1002/asia.201301011


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