| 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 %.
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											Authors
												Luca Mantilli, Clément Mazet, 
											