An efficient transition-metal-free amination of benzoxazoles has been developed. With catalytic amounts of tetrabutylammoniumiodide (TBAI), aqueous solutions of H2O2 or TBHP as co-oxidant and under mild reaction conditions, highly desirable 2-aminobenzoxazoles were isolated in excellent yields of up to 93%. First mechanistic experiments indicate the in situ iodination of the secondary amine as the putative mode of activation.
Org. Lett., 2011, 13 (14), pp 3754–3757
DOI: 10.1021/ol201439t
https://pubs.acs.org/doi/abs/10.1021/ol201439t
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