Epoxidation of Terminal Alkenes with Chiral Pt Complexes

platinum - epoxidation - olefins - P-ligands

Significance

Asymmetric epoxidation of alkenes is a very well known reaction that has been studied utilizing a range of chiral catalysts. However, unfunctionalized terminal olefins remain challenging because of their inherent low reactivity and the difficulty to distinguish the two prochiral faces. This new catalyst was found to be highly reactive and selective for unfunctionalized terminal alkenes.

Comment

The use of hydrogen peroxide and a highly reactive Pt complex makes this an attractive system for use in asymmetric epoxidation. Furthermore, the high selectivity for less reactive terminal alkenes makes this method more impressive. The high yields, chemoselectivity, and enantio­selectivity with a broad substrate scope show that this simple system could be applied to many situations in organic chemistry.