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Polyfluoroarylation of oxazolones: access to non-natural fluorinated amino acids
Kip A Teegardin1, Jimmie D Weaver
1Department of Chemistry, Oklahoma State University, Stillwater, OK 74078, USA. jimmie.weaver@okstate.edu.
Chemical Communications (Cambridge, England)
|March 31, 2017
Abstract:
Herein, conditions are provided for the formation and use of the oxazolone enolate for the nucleophilic substitution of highly fluorinated (hetero)arenes, which after unmasking yield highly fluorinated non-natural amino acids and derivatives. In addition, the properties and chemical behavior of this new class of amino acids are explored. The utility is demonstrated in the one pot synthesis of medicinally relevant 2-aminohydantoins.