Please use this identifier to cite or link to this item: https://doi.org/10.1039/c3cc00019b
DC FieldValue
dc.titleA macrocyclic aromatic pyridone pentamer as a highly efficient organocatalyst for the direct arylations of unactivated arenes
dc.contributor.authorZhao, H.
dc.contributor.authorShen, J.
dc.contributor.authorGuo, J.
dc.contributor.authorYe, R.
dc.contributor.authorZeng, H.
dc.date.accessioned2014-06-23T05:30:24Z
dc.date.available2014-06-23T05:30:24Z
dc.date.issued2013-03-21
dc.identifier.citationZhao, H., Shen, J., Guo, J., Ye, R., Zeng, H. (2013-03-21). A macrocyclic aromatic pyridone pentamer as a highly efficient organocatalyst for the direct arylations of unactivated arenes. Chemical Communications 49 (23) : 2323-2325. ScholarBank@NUS Repository. https://doi.org/10.1039/c3cc00019b
dc.identifier.issn13597345
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75442
dc.description.abstractA macrocyclic aromatic pyridone pentamer was shown to catalyze highly efficient transition-metal-free arylations of unactivated aromatic C-H bonds with aryl iodides and bromides in the presence of potassium tert-butoxide. This journal is © The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c3cc00019b
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c3cc00019b
dc.description.sourcetitleChemical Communications
dc.description.volume49
dc.description.issue23
dc.description.page2323-2325
dc.description.codenCHCOF
dc.identifier.isiut000315169400015
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