| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5227111 | Tetrahedron | 2009 | 7 Pages |
Abstract
The stereoselective synthesis of the sex pheromone of horse-chestnut leafminer was efficiently carried out using methodology based on the Pd(0)-catalyzed cross-coupling of 1-pentynylmagnesium bromide with the corresponding vinyl iodides as the key step.
Graphical abstractSynthesis of sex pheromone of horse-chestnut leafminer (1) has been achieved by the palladium-catalyzed cross-coupling reaction of 1-pentynylmagnesium bromide and suitable vinyl iodides as the key step to construct the conjugated diene moiety of the title compound.Download full-size image
Related Topics
Physical Sciences and Engineering
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Authors
Jacek Grodner,