Highly Efficient Palladium-Catalyzed Allylic Alkylation of Cyanoacetamides with Controllable and Chemoselective Mono- and Double Substitutions

The front cover artwork for Issue 22/2016 is provided by Zi‐Wei Gao and Li‐Wen Xu's group of Shaanxi Normal University. The image shows a novel palladium catalyst system combined with a triazine‐modified new phosphine ligand that was developed successfully for the catalytic allylic alkylation o...

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Bibliographic Details
Published in:ChemCatChem 2016-11, Vol.8 (22), p.3420-3420
Main Authors: Gao, Pei-Sen, Li, Ning, Zhang, Jin-Lei, Zhu, Zhuang-Li, Gao, Zi-Wei, Sun, Hua-Ming, Zhang, Wei-Qiang, Xu, Li-Wen
Format: Article
Language:English
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Summary:The front cover artwork for Issue 22/2016 is provided by Zi‐Wei Gao and Li‐Wen Xu's group of Shaanxi Normal University. The image shows a novel palladium catalyst system combined with a triazine‐modified new phosphine ligand that was developed successfully for the catalytic allylic alkylation of various cyanoacetamides. See the Full Paper itself at http://dx.doi.org/10.1002/cctc.201601021. “The triazine‐modified phosphine ligand developed for the palladium‐catalyzed allylic alkylation of cyanoacetamides greatly promotes controllable monoallylation and double allylation in environmentally benign and recyclable PEG‐400 (PEG=poly(ethylene glycol)).” This and more about the story behind the research featured on the front cover can be found in this issue's Cover Profile. Read the full text of the corresponding research at http://dx.doi.org/10.1002/cctc.201601021.
ISSN:1867-3880
1867-3899
DOI:10.1002/cctc.201601400