Palladium-catalyzed C-H activation/C-C cross-coupling reactions electrochemistry
Palladium-catalyzed C-H activation/C-C cross-coupling reactions typically require stoichiometric chemical oxidants and exogenous ligands. However, there are significant disadvantages associated with the use of traditional stoichiometric oxidants. To overcome these issues, we have developed an electr...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2017-11, Vol.53 (9), p.12189-12192 |
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container_title | Chemical communications (Cambridge, England) |
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creator | Ma, Cong Zhao, Chuan-Qi Li, Yi-Qian Zhang, Li-Pu Xu, Xue-Tao Zhang, Kun Mei, Tian-Sheng |
description | Palladium-catalyzed C-H activation/C-C cross-coupling reactions typically require stoichiometric chemical oxidants and exogenous ligands. However, there are significant disadvantages associated with the use of traditional stoichiometric oxidants. To overcome these issues, we have developed an electrochemical strategy to achieve methylation and acylation.
Palladium-catalyzed C(sp
2
)-H methylation and acylation
via
anodic oxidation have been developed to avoid the use of stoichiometric chemical oxidants. |
doi_str_mv | 10.1039/c7cc07429h |
format | Article |
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Palladium-catalyzed C(sp
2
)-H methylation and acylation
via
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Palladium-catalyzed C(sp
2
)-H methylation and acylation
via
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Palladium-catalyzed C(sp
2
)-H methylation and acylation
via
anodic oxidation have been developed to avoid the use of stoichiometric chemical oxidants.</abstract><doi>10.1039/c7cc07429h</doi><tpages>4</tpages></addata></record> |
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title | Palladium-catalyzed C-H activation/C-C cross-coupling reactions electrochemistry |
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