Vanadium-catalyzed enantioselective oxidation of allyl sulfides

Add time:08/27/2019    Source:sciencedirect.com

The enantioselective oxidation of allyl sulfides with a vanadyl complex of 3,5-diiodosalicylidene tert-leucinol as a catalyst and aqueous hydrogen peroxide as an oxidant afforded chiral allyl sulfoxides with high enantioselectivities of up to 97.3% ee and moderate yields.

We also recommend Trading Suppliers and Manufacturers of Isobutyl(o-tolyl) sulfide (cas 15561-00-9). Pls Click Website Link as below: cas 15561-00-9 suppliers

Prev:Stereoselective addition of Grignard reagents to (2-methyl-5-tert-butyl)phenyl 1-thio-β-D-ribopentodialdo-1,4-furanoside derivative
Next:Stereoselective oxidation of aromatic sulfides and sulfoxides in the binding domain of bovine serum albumin)