Please use this identifier to cite or link to this item:
https://doi.org/10.1021/ol402579x
DC Field | Value | |
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dc.title | A facile approach for the asymmetric synthesis of oxindoles with a 3-sulfenyl-substituted quaternary stereocenter | |
dc.contributor.author | Dou, X. | |
dc.contributor.author | Zhou, B. | |
dc.contributor.author | Yao, W. | |
dc.contributor.author | Zhong, F. | |
dc.contributor.author | Jiang, C. | |
dc.contributor.author | Lu, Y. | |
dc.date.accessioned | 2014-06-23T05:30:00Z | |
dc.date.available | 2014-06-23T05:30:00Z | |
dc.date.issued | 2013-10-04 | |
dc.identifier.citation | Dou, X., Zhou, B., Yao, W., Zhong, F., Jiang, C., Lu, Y. (2013-10-04). A facile approach for the asymmetric synthesis of oxindoles with a 3-sulfenyl-substituted quaternary stereocenter. Organic Letters 15 (19) : 4920-4923. ScholarBank@NUS Repository. https://doi.org/10.1021/ol402579x | |
dc.identifier.issn | 15237060 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/75410 | |
dc.description.abstract | With the employment of a threonine-incorporating multifunctional catalyst 9, Michael addition of 3-sulfenyloxindoles to nitroolefins proceeded stereoselectively, leading to the formation of oxindoles with a 3-sulfenyl-substituted quaternary center in excellent yields, and with high diastereoselectivities and excellent enantioselectivities. © 2013 American Chemical Society. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol402579x | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.description.doi | 10.1021/ol402579x | |
dc.description.sourcetitle | Organic Letters | |
dc.description.volume | 15 | |
dc.description.issue | 19 | |
dc.description.page | 4920-4923 | |
dc.description.coden | ORLEF | |
dc.identifier.isiut | 000326320200002 | |
Appears in Collections: | Staff Publications |
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