Selective CO bond formation: highly efficient radical dioxygenation of alkenes initiated by catalytic amount of tert-butyl hydroperoxide

Add time:07/11/2019    Source:sciencedirect.com

A highly selective radical dioxygenation of alkenes using hydroxamic acid and O2 with 5–10 mol % of tert-butyl hydroperoxide as a catalyst was developed. On the basis of this newly developed strategy, a wide range of phenylethanol derivatives with a variety of functional groups can be effectively synthesized.

We also recommend Trading Suppliers and Manufacturers of (4-Bromo-2-fluoro-5-methyl-phenyl)-carbamic acid tert-butyl ester (cas 1260804-94-1). Pls Click Website Link as below: cas 1260804-94-1 suppliers

Prev:Attempts to cathodically reduce boron oxides to borohydride in aqueous solution
Next:The effects of urolithins on the response of prostate cancer cells to non-steroidal antiandrogen bicalutamide)