Please use this identifier to cite or link to this item:
http://repository.aaup.edu/jspui/handle/123456789/115
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | hisham qrareya | - |
dc.contributor.author | stefano protti, $Other$Other | - |
dc.contributor.author | maurizio fagnoni., $Other$Other | - |
dc.date.accessioned | 2020-01-10T09:10:32Z | - |
dc.date.available | 2020-01-10T09:10:32Z | - |
dc.date.issued | 2014 | - |
dc.identifier.uri | http://repository.aaup.edu/jspui/handle/123456789/115 | - |
dc.description.abstract | Some oxygen-bonded substituents were investigated as leaving groups in photoinduced ArSN1 reactions. Irradiation of aryl imidazylates and of the corresponding imidazolium salts mainly caused homolysis of the ArO?S bond. However, previously unexplored tri?uoroethoxy aryl sulfates were found to undergo e?cient metal-free arylation. The sulfates were conveniently generated in situ by dissolving the corresponding imidazolium salts in basic 2,2,2-tri?uoroethanol. | en_US |
dc.publisher | Journal of Organic Chemistry (JOC). | en_US |
dc.subject | ArSN1 reaction | en_US |
dc.subject | metal-free arylation. | en_US |
dc.title | Aryl imidazylates and aryl sulfates. Novel electrophiles in metal-free ArSN1 reactions | en_US |
dc.type | Article | en_US |
Appears in Collections: | Faculty & Staff Scientific Research publications |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
Admin Tools