An oxidative carbon-carbon bond-forming reaction proceeds via an isolable iminium ion

The mechanism of our previously reported DDQ-mediated oxidative C-C bond-forming reaction is investigated. We are able to trap and characterize an iminium ion intermediate with X-ray crystallography, elemental analysis, and solid-state NMR spectroscopy; to our knowledge this is the first time this p...

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Bibliographic Details
Main Authors: Tsang, Althea S.-K. (Author) , Jensen, Paul (Author) , Hook, James M. (Author) , Hashmi, A. Stephen K. (Author) , Todd, Matthew H. (Author)
Format: Article (Journal)
Language:German
Published: 7. Februar 2011
In: Pure and applied chemistry
Year: 2011, Volume: 83, Issue: 3, Pages: 655-665
ISSN:1365-3075
DOI:10.1351/PAC-CON-11-01-01
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1351/PAC-CON-11-01-01
Verlag, lizenzpflichtig, Volltext: https://www.degruyterbrill.com/document/doi/10.1351/PAC-CON-11-01-01/html
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Author Notes:Althea S.-K. Tsang, Paul Jensen, James M. Hook, A. Stephen K. Hashmi, and Matthew H. Todd
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Summary:The mechanism of our previously reported DDQ-mediated oxidative C-C bond-forming reaction is investigated. We are able to trap and characterize an iminium ion intermediate with X-ray crystallography, elemental analysis, and solid-state NMR spectroscopy; to our knowledge this is the first time this putative intermediate ion has been directly observed in such cross-dehydrogenative couplings (CDCs). The intermediate can be reacted with a range of nucleo-philes, including a malonate that is not amenable to a one-pot reaction protocol.
Item Description:Gesehen am 17.11.2022
Physical Description:Online Resource
ISSN:1365-3075
DOI:10.1351/PAC-CON-11-01-01