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Please use this identifier to cite or link to this item: https://doi.org/10.1039/c1cc14377h
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dc.titleBOP-mediated one-pot synthesis of C5-symmetric macrocyclic pyridone pentamers
dc.contributor.authorDu, Z.
dc.contributor.authorRen, C.
dc.contributor.authorYe, R.
dc.contributor.authorShen, J.
dc.contributor.authorMaurizot, V.
dc.contributor.authorLu, Y.
dc.contributor.authorWang, J.
dc.contributor.authorZeng, H.
dc.date.accessioned2014-10-16T08:21:41Z
dc.date.available2014-10-16T08:21:41Z
dc.date.issued2011-12-14
dc.identifier.citationDu, Z., Ren, C., Ye, R., Shen, J., Maurizot, V., Lu, Y., Wang, J., Zeng, H. (2011-12-14). BOP-mediated one-pot synthesis of C5-symmetric macrocyclic pyridone pentamers. Chemical Communications 47 (46) : 12488-12490. ScholarBank@NUS Repository. https://doi.org/10.1039/c1cc14377h
dc.identifier.issn13597345
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93211
dc.description.abstractWe report here, for the first time, the BOP-mediated one-pot macrocyclization that is facilitated and guided by internally placed intramolecular H-bonds to allow for the highly selective formation of five-residue cation-binding macrocycles. © 2011 The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c1cc14377h
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c1cc14377h
dc.description.sourcetitleChemical Communications
dc.description.volume47
dc.description.issue46
dc.description.page12488-12490
dc.description.codenCHCOF
dc.identifier.isiut000296985100018
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