Please use this identifier to cite or link to this item: https://doi.org/10.1039/c2ob25160d
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dc.titleFolding-promoted TBAX-mediated selective demethylation of methoxybenzene-based macrocyclic aromatic pentamers
dc.contributor.authorDu, Z.
dc.contributor.authorQin, B.
dc.contributor.authorSun, C.
dc.contributor.authorLiu, Y.
dc.contributor.authorZheng, X.
dc.contributor.authorZhang, K.
dc.contributor.authorConney, A.H.
dc.contributor.authorZeng, H.
dc.date.accessioned2014-06-23T05:39:51Z
dc.date.available2014-06-23T05:39:51Z
dc.date.issued2012-06-07
dc.identifier.citationDu, Z., Qin, B., Sun, C., Liu, Y., Zheng, X., Zhang, K., Conney, A.H., Zeng, H. (2012-06-07). Folding-promoted TBAX-mediated selective demethylation of methoxybenzene-based macrocyclic aromatic pentamers. Organic and Biomolecular Chemistry 10 (21) : 4164-4171. ScholarBank@NUS Repository. https://doi.org/10.1039/c2ob25160d
dc.identifier.issn14770520
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76203
dc.description.abstractDescribed in this study is the ability of tetrabutylammonium salts (TBAX) to mediate an efficient mono- or di-demethylation removing one or two out of five aromatic methoxy methyl groups situated in similar chemical microenvironments in a H-bonded macrocyclic aromatic pentamer. These demethylations are found to be both chemo- and regioselective, and promoted by the H-bonding directed folding of the macrocyclic backbone. This journal is © 2012 The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c2ob25160d
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c2ob25160d
dc.description.sourcetitleOrganic and Biomolecular Chemistry
dc.description.volume10
dc.description.issue21
dc.description.page4164-4171
dc.description.codenOBCRA
dc.identifier.isiut000303768700003
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