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J Org Chem ; 79(20): 9613-8, 2014 Oct 17.
Article in English | MEDLINE | ID: mdl-25255384

ABSTRACT

An electrochemically promoted coupling of benzoxazoles and amines has been developed, leading directly to the formation of 2-aminobenzoxazoles. The chemistry utilizes catalytic quantities of a tetraalkylammonium halide redox catalyst and is carried out under constant current conditions in a simple undivided cell. The use of excess chemical oxidant or large amounts of supporting electrolyte is avoided. This greatly simplifies the workup and isolation process and leads to a reduction in waste.


Subject(s)
Benzoxazoles/chemistry , Halogens/chemistry , Quaternary Ammonium Compounds/chemistry , Amination , Catalysis , Molecular Structure , Oxidation-Reduction
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