Please use this identifier to cite or link to this item:
https://doi.org/10.1021/cs300628w
DC Field | Value | |
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dc.title | Highly efficient assembly of 3-hydroxy oxindole scaffold via a catalytic decarboxylative [1,2]-addition strategy | |
dc.contributor.author | Ren, Q. | |
dc.contributor.author | Huang, J. | |
dc.contributor.author | Wang, L. | |
dc.contributor.author | Li, W. | |
dc.contributor.author | Liu, H. | |
dc.contributor.author | Jiang, X. | |
dc.contributor.author | Wang, J. | |
dc.date.accessioned | 2014-05-19T02:52:33Z | |
dc.date.available | 2014-05-19T02:52:33Z | |
dc.date.issued | 2012-12-07 | |
dc.identifier.citation | Ren, 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.issn | 21555435 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/52976 | |
dc.description.abstract | The 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.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/cs300628w | |
dc.source | Scopus | |
dc.subject | 1,2-addition | |
dc.subject | decarboxylation | |
dc.subject | organocatalysis | |
dc.subject | oxindole | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.contributor.department | PHYSICS | |
dc.description.doi | 10.1021/cs300628w | |
dc.description.sourcetitle | ACS Catalysis | |
dc.description.volume | 2 | |
dc.description.issue | 12 | |
dc.description.page | 2622-2625 | |
dc.identifier.isiut | 000312170100023 | |
Appears in Collections: | Staff Publications |
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