| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1327878 | Journal of Organometallic Chemistry | 2005 | 5 Pages |
Abstract
The Heck coupling of ArN2BF4 with secondary allylic alcohols, carried out in methanol using Pd(dba)2 as catalyst without extra ligands and base, leads to the corresponding β-arylated carbonyl compounds. Such conditions afford arylated acetals from primary allylic alcohols.
Graphical abstractThe Heck coupling of ArN2BF4 with allylic alcohols has been carried out in methanol using Pd(dba)2 as catalyst in the absence of extra ligand and base.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Judit Masllorens, Sandrine Bouquillon, Anna Roglans, Françoise Hénin, Jacques Muzart,