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https://hdl.handle.net/10356/99248
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Huang, Zhiyan | en |
dc.contributor.author | Lim, Li Hui | en |
dc.contributor.author | Chen, Zuliang | en |
dc.contributor.author | Li, Yongxin | en |
dc.contributor.author | Zhou, Feng | en |
dc.contributor.author | Su, Haibin | en |
dc.contributor.author | Zhou, Jianrong Steve | en |
dc.date.accessioned | 2013-11-12T05:38:45Z | en |
dc.date.accessioned | 2019-12-06T20:05:02Z | - |
dc.date.available | 2013-11-12T05:38:45Z | en |
dc.date.available | 2019-12-06T20:05:02Z | - |
dc.date.copyright | 2013 | en |
dc.date.issued | 2013 | en |
dc.identifier.issn | 1433-7851 | en |
dc.identifier.uri | https://hdl.handle.net/10356/99248 | - |
dc.description.abstract | Weak is powerful: For the arylation of tin enolates, the palladium catalyst engages in weak CH=O hydrogen bonds to control stereoselectivity (see scheme). Similar catalysts capable of NH=O hydrogen bonding also works well. | en |
dc.language.iso | en | en |
dc.relation.ispartofseries | Angewandte chemie international edition | en |
dc.rights | © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim | en |
dc.title | Arene CH=O hydrogen bonding : a stereocontrolling tool in palladium-catalyzed arylation and vinylation of ketones | en |
dc.type | Journal Article | en |
dc.contributor.school | School of Materials Science & Engineering | en |
dc.contributor.school | School of Physical and Mathematical Sciences | en |
dc.identifier.doi | 10.1002/anie.201300621 | en |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
Appears in Collections: | MSE Journal Articles SPMS Journal Articles |
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