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Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol2016466
DC FieldValue
dc.titleAn unexpected oxidation of unactivated methylene C-H using DIB/TBHP protocol
dc.contributor.authorZhao, Y.
dc.contributor.authorYim, W.-L.
dc.contributor.authorTan, C.K.
dc.contributor.authorYeung, Y.-Y.
dc.date.accessioned2014-06-23T05:31:57Z
dc.date.available2014-06-23T05:31:57Z
dc.date.issued2011-08-19
dc.identifier.citationZhao, 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.issn15237060
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75569
dc.description.abstractAn 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.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol2016466
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ol2016466
dc.description.sourcetitleOrganic Letters
dc.description.volume13
dc.description.issue16
dc.description.page4308-4311
dc.identifier.isiut000293759100040
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