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.
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Larsen, Casey
R.; Grotjahn, Douglas B. (2016). Stereoselective Alkene
Isomerization over One Position. ACS Publications. Collection. https://doi.org/10.1021/ja3036477