American Chemical Society
Browse

Stereoselective Alkene Isomerization over One Position

Posted on 2012-06-27 - 00:00
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.

CITE THIS COLLECTION

DataCite
No result found
or
Select your citation style and then place your mouse over the citation text to select it.

SHARE

email
need help?