4.3 Article

TEMPO/PhI(OAc)2-mediated Direct Sulfoximination of Benzoxazoles under Metal-free Conditions

Journal

CHEMISTRY LETTERS
Volume 51, Issue 7, Pages 756-759

Publisher

CHEMICAL SOC JAPAN
DOI: 10.1246/cl.220177

Keywords

Sulfoximines; Benzoxazoles; C-N bond formation

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A metal-free reaction system utilizing TEMPO and PhI(OAc)(2) has been developed for the oxidative C-N coupling of benzoxazoles with NH-sulfoximines, resulting in moderate to high yields of corresponding 2-iminoazoles under ambient atmosphere without any metal catalyst at room temperature.
A metal-free reaction system consisting of TEMPO and PhI(OAc)(2) for the oxidative C-N coupling of benzoxazoles with NH-sulfoximines has been developed. The reaction can proceed under ambient atmosphere without any metal catalyst at room temperature to afford the corresponding 2-iminoazoles in moderate to high yields.

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