Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5272198 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
The isomerization of primary allylic alcohols into the corresponding aldehydes has been accomplished using an analogue of Crabtree's iridium hydrogenation catalyst and by adequately tuning the experimental conditions. A wide range of substrates is converted quantitatively into the desired aldehyde at room temperature in expedient reaction times by using catalyst loading as low as 0.25 mol %.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Luca Mantilli, Clément Mazet,