Stereoselective alkene isomerization over one position

J Am Chem Soc. 2012 Jun 27;134(25):10357-60. doi: 10.1021/ja3036477. Epub 2012 Jun 15.

Abstract

Although controlling both the position of the double bond and E:Z selectivity in alkene isomerization is difficult, 1 is a very efficient catalyst for selective mono-isomerization of a variety of multifunctional alkenes to afford >99.5% E-products. Many reactions are complete within 10 min at room temperature. Even sensitive enols and enamides susceptible to further reaction can be generated. Catalyst loadings in the 0.01-0.1 mol% range can be employed. E-to-Z isomerization of the product from diallyl ether was only <10(-6) times as fast as its formation, showing the extremely high kinetic selectivity of 1.