Literature DB >> 16092883

An unusual radical Smiles rearrangement.

Eric Bacqué1, Myriem El Qacemi, Samir Z Zard.   

Abstract

Radicals derived from N-(alpha-xanthyl)acetanilides or N-(alpha-xanthyl)acetylaminopyridines possessing a substituent next to the nitrogen undergo a hitherto undocumented Smiles rearrangement proceeding through a four-membered ring. It was also found that under certain conditions the amidyl radical produced by cleavage of the four-membered ring intermediate can undergo fragmentation to give an isocyanate. Such fragmentations are unprecedented at temperatures corresponding to refluxing benzene or chlorobenzene. [reaction: see text]

Entities:  

Year:  2005        PMID: 16092883     DOI: 10.1021/ol051568l

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

Review 1.  Aryl Transfer Strategies Mediated by Photoinduced Electron Transfer.

Authors:  Anthony R Allen; Efrey A Noten; Corey R J Stephenson
Journal:  Chem Rev       Date:  2021-10-21       Impact factor: 72.087

2.  Facile Smiles-type rearrangement in radical cations of N-acyl arylsulfonamides and analogs.

Authors:  Karl K Irikura; Nino G Todua
Journal:  Rapid Commun Mass Spectrom       Date:  2014-04-15       Impact factor: 2.419

3.  Radical Aryl Migration from Boron to Carbon.

Authors:  Dinghai Wang; Christian Mück-Lichtenfeld; Constantin G Daniliuc; Armido Studer
Journal:  J Am Chem Soc       Date:  2021-06-20       Impact factor: 15.419

  3 in total

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