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Please use this identifier to cite or link to this item: https://doi.org/10.1002/anie.201208285
DC FieldValue
dc.titleChiral phosphine catalyzed asymmetric michael addition of oxindoles
dc.contributor.authorZhong, F.
dc.contributor.authorDou, X.
dc.contributor.authorHan, X.
dc.contributor.authorYao, W.
dc.contributor.authorZhu, Q.
dc.contributor.authorMeng, Y.
dc.contributor.authorLu, Y.
dc.date.accessioned2014-06-23T05:34:14Z
dc.date.available2014-06-23T05:34:14Z
dc.date.issued2013-01-14
dc.identifier.citationZhong, F., Dou, X., Han, X., Yao, W., Zhu, Q., Meng, Y., Lu, Y. (2013-01-14). Chiral phosphine catalyzed asymmetric michael addition of oxindoles. Angewandte Chemie - International Edition 52 (3) : 943-947. ScholarBank@NUS Repository. https://doi.org/10.1002/anie.201208285
dc.identifier.issn14337851
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75753
dc.description.abstractBifunctional phosphines derived from amino acids mediate the asymmetric Michael addition of 3-substituted oxindoles to activated alkenes (see scheme). Biologically relevant chiral 3,3-disubstituted oxindoles were thus prepared in high yields and with excellent enantioselectivities from 3-aryl- and 3-alkyl-substituted oxindoles and various activated alkenes. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/anie.201208285
dc.sourceScopus
dc.subjectalkenes
dc.subjectamino acids
dc.subjectbifunctional phosphines
dc.subjectMichael addition
dc.subjectoxindoles
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1002/anie.201208285
dc.description.sourcetitleAngewandte Chemie - International Edition
dc.description.volume52
dc.description.issue3
dc.description.page943-947
dc.description.codenACIEF
dc.identifier.isiut000313688100026
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