Please use this identifier to cite or link to this item:
https://doi.org/10.1021/ol2016466
DC Field | Value | |
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dc.title | An unexpected oxidation of unactivated methylene C-H using DIB/TBHP protocol | |
dc.contributor.author | Zhao, Y. | |
dc.contributor.author | Yim, W.-L. | |
dc.contributor.author | Tan, C.K. | |
dc.contributor.author | Yeung, Y.-Y. | |
dc.date.accessioned | 2014-06-23T05:31:57Z | |
dc.date.available | 2014-06-23T05:31:57Z | |
dc.date.issued | 2011-08-19 | |
dc.identifier.citation | Zhao, Y., Yim, W.-L., Tan, C.K., Yeung, Y.-Y. (2011-08-19). An unexpected oxidation of unactivated methylene C-H using DIB/TBHP protocol. Organic Letters 13 (16) : 4308-4311. ScholarBank@NUS Repository. https://doi.org/10.1021/ol2016466 | |
dc.identifier.issn | 15237060 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/75569 | |
dc.description.abstract | An in situ generated hypervalent iodine species, bis(tert-butylperoxy) iodobenzene, was used as a peroxy radical source for the oxidation of unreactive, remote, and isolated alkyl (cyclic or aliphatic) esters and amides to the corresponding keto compounds under very mild conditions. © 2011 American Chemical Society. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol2016466 | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.description.doi | 10.1021/ol2016466 | |
dc.description.sourcetitle | Organic Letters | |
dc.description.volume | 13 | |
dc.description.issue | 16 | |
dc.description.page | 4308-4311 | |
dc.identifier.isiut | 000293759100040 | |
Appears in Collections: | Staff Publications |
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