Please use this identifier to cite or link to this item: https://doi.org/10.1021/cs300628w
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dc.titleHighly efficient assembly of 3-hydroxy oxindole scaffold via a catalytic decarboxylative [1,2]-addition strategy
dc.contributor.authorRen, Q.
dc.contributor.authorHuang, J.
dc.contributor.authorWang, L.
dc.contributor.authorLi, W.
dc.contributor.authorLiu, H.
dc.contributor.authorJiang, X.
dc.contributor.authorWang, J.
dc.date.accessioned2014-05-19T02:52:33Z
dc.date.available2014-05-19T02:52:33Z
dc.date.issued2012-12-07
dc.identifier.citationRen, Q., Huang, J., Wang, L., Li, W., Liu, H., Jiang, X., Wang, J. (2012-12-07). Highly efficient assembly of 3-hydroxy oxindole scaffold via a catalytic decarboxylative [1,2]-addition strategy. ACS Catalysis 2 (12) : 2622-2625. ScholarBank@NUS Repository. https://doi.org/10.1021/cs300628w
dc.identifier.issn21555435
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/52976
dc.description.abstractThe 3-hydroxy-2-oxindole scaffold is being continuously discovered to be at the core of a diverse set of natural products. Herein, we document a highly efficient catalytic decarboxylative [1,2]-addition strategy to quickly assemble this scaffold, using a catalytic amount of weak base. © 2012 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/cs300628w
dc.sourceScopus
dc.subject1,2-addition
dc.subjectdecarboxylation
dc.subjectorganocatalysis
dc.subjectoxindole
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.contributor.departmentPHYSICS
dc.description.doi10.1021/cs300628w
dc.description.sourcetitleACS Catalysis
dc.description.volume2
dc.description.issue12
dc.description.page2622-2625
dc.identifier.isiut000312170100023
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