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Harnessing triaryloxonium ions for aryne generation

Abstract:
Arynes are highly reactive and versatile intermediates for the functionalization of aromatic rings that are often generated using strong bases or fluoride sources, which, in some cases, can limit functional group tolerance. Here we demonstrate that triaryloxonium ions can be transformed into arynes through treatment with solid potassium phosphate at room temperature. A substantial range of functional group-bearing arynes, including 4,5-pyrimidynes, may be generated and trapped using cycloaddition reactions with high yields. Other arynophiles including nitrones, alkenes and azides are compatible with these conditions. Quantum computation in conjunction with an intramolecular kinetic isotope study is consistent with an elimination, unimolecular, conjugate base-like mechanism of elimination to form the aryne. These investigations demonstrate that the oxonium ion is a powerful electron-withdrawing group and a particularly effective leaving group. We anticipate that this study will stimulate further investigations into the synthetic utility of aryl oxonium ions.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s44160-023-00408-1

Authors


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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry Research Laboratory
Role:
Author
ORCID:
0000-0002-3983-8105
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry Research Laboratory
Role:
Author
More by this author
Role:
Author
ORCID:
0000-0001-8598-291X
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry Research Laboratory
Role:
Author
More by this author
Role:
Author
ORCID:
0000-0002-0104-4166


Publisher:
Springer Nature
Journal:
Nature Synthesis More from this journal
Volume:
3
Issue:
1
Pages:
58–66
Publication date:
2023-10-02
Acceptance date:
2023-08-31
DOI:
ISSN:
2731-0582


Language:
English
Keywords:
Pubs id:
1546128
Local pid:
pubs:1546128
Deposit date:
2023-10-31

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