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Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol202658p
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dc.titleFolding-promoted TBACl-mediated chemo- and regioselective demethylations of methoxybenzene-based macrocyclic pentamers
dc.contributor.authorQin, B.
dc.contributor.authorJiang, L.
dc.contributor.authorShen, S.
dc.contributor.authorSun, C.
dc.contributor.authorYuan, W.
dc.contributor.authorLi, S.F.Y.
dc.contributor.authorZeng, H.
dc.date.accessioned2014-06-23T05:39:50Z
dc.date.available2014-06-23T05:39:50Z
dc.date.issued2011-12-02
dc.identifier.citationQin, B., Jiang, L., Shen, S., Sun, C., Yuan, W., Li, S.F.Y., Zeng, H. (2011-12-02). Folding-promoted TBACl-mediated chemo- and regioselective demethylations of methoxybenzene-based macrocyclic pentamers. Organic Letters 13 (23) : 6212-6215. ScholarBank@NUS Repository. https://doi.org/10.1021/ol202658p
dc.identifier.issn15237060
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76202
dc.description.abstractTetrabutylammonium chloride (TBACl) salt alone has not been shown previously to be capable of removing methoxy groups. It is demonstrated here that the use of TBACl achieves efficient folding-promoted chemo- and regioselective demethylations, eliminating up to two out of five methyl groups situated in similar macrocyclic chemical microenvironments. © 2011 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol202658p
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ol202658p
dc.description.sourcetitleOrganic Letters
dc.description.volume13
dc.description.issue23
dc.description.page6212-6215
dc.identifier.isiut000297274700020
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