Please use this identifier to cite or link to this item:
https://doi.org/10.1039/c3cc00019b
DC Field | Value | |
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dc.title | A macrocyclic aromatic pyridone pentamer as a highly efficient organocatalyst for the direct arylations of unactivated arenes | |
dc.contributor.author | Zhao, H. | |
dc.contributor.author | Shen, J. | |
dc.contributor.author | Guo, J. | |
dc.contributor.author | Ye, R. | |
dc.contributor.author | Zeng, H. | |
dc.date.accessioned | 2014-06-23T05:30:24Z | |
dc.date.available | 2014-06-23T05:30:24Z | |
dc.date.issued | 2013-03-21 | |
dc.identifier.citation | Zhao, 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.issn | 13597345 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/75442 | |
dc.description.abstract | A 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.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c3cc00019b | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.description.doi | 10.1039/c3cc00019b | |
dc.description.sourcetitle | Chemical Communications | |
dc.description.volume | 49 | |
dc.description.issue | 23 | |
dc.description.page | 2323-2325 | |
dc.description.coden | CHCOF | |
dc.identifier.isiut | 000315169400015 | |
Appears in Collections: | Staff Publications |
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