Organocatalytic Dakin oxidation by nucleophilic flavin catalysts.
Shuai Chen, Mohammad S Hossain, Frank W Foss
Index: Org. Lett. 14(11) , 2806-9, (2012)
Full Text: HTML
Abstract
Flavin catalysts perform the first organocatalytic Dakin oxidation of electron-rich arylaldehydes to phenols under mild, basic conditions. Catechols are readily prepared, and the oxidation of 2-hydroxyacetophenone was achieved. Aerobic oxidation is displayed in the presence of Zn(0) as a reducing agent. This reactivity broadens the scope of biomimetic flavin catalysis in the realm of nucleophilic oxidations, providing a framework for mechanistic investigations for related oxidations, such as the Baeyer-Villiger oxidation and Weitz-Scheffer epoxidation.
Related Compounds
Related Articles:
2011-01-01
[Bioresour. Technol. 102(2) , 483-9, (2011)]
2012-08-06
[Inorg. Chem. 51(15) , 8241-53, (2012)]
2013-09-01
[Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 113 , 393-9, (2013)]
2008-02-01
[Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 69(2) , 664-9, (2008)]
2012-10-01
[Chemistry 18(40) , 12595-8, (2012)]