Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/93146
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dc.titleAsymmetric organocatalytic decarboxylative Mannich reaction using β-keto acids: A new protocol for the synthesis of chiral â-amino ketones
dc.contributor.authorJiang, C.
dc.contributor.authorZhong, F.
dc.contributor.authorLu, Y.
dc.date.accessioned2014-10-16T08:20:57Z
dc.date.available2014-10-16T08:20:57Z
dc.date.issued2012-08-13
dc.identifier.citationJiang, C., Zhong, F., Lu, Y. (2012-08-13). Asymmetric organocatalytic decarboxylative Mannich reaction using β-keto acids: A new protocol for the synthesis of chiral â-amino ketones. Beilstein Journal of Organic Chemistry 8 : 1279-1283. ScholarBank@NUS Repository.
dc.identifier.issn18605397
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93146
dc.description.abstractThe first decarboxylative Mannich reaction employing β-keto acids, catalyzed by cinchonine-derived bifunctional thiourea catalyst has been described. The desired â-amino ketones were obtained in excellent yields and with moderate to good enantioselectivities. © 2012 Jiang et al.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.3762/bjoc.8.144
dc.sourceScopus
dc.subjectβ-keto acid
dc.subjectDecarboxylative addition
dc.subjectMannich reaction
dc.subjectOrganocatalysis
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.sourcetitleBeilstein Journal of Organic Chemistry
dc.description.volume8
dc.description.page1279-1283
dc.description.codenBJOCB
dc.identifier.isiut000307439700001
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