𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mild Conditions for Copper-Catalyzed Coupling Reaction of Phenols and Aryl Iodides and Bromides

✍ Scribed by Armelle Ouali; Jean-Francis Spindler; Henri-Jean Cristau; Marc Taillefer

Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
211 KB
Volume
348
Category
Article
ISSN
1615-4150

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Mild and Efficient Copper-Catalyzed Cyan
Mild and Efficient Copper-Catalyzed Cyanation of Aryl Iodides and Bromides
✍ Henri-Jean Cristau; Armelle Ouali; Jean-Francis Spindler; Marc Taillefer πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 212 KB

## Abstract An efficient copper‐catalyzed cyanation of aryl iodides and bromides is reported. Our system combines catalytic amounts of both copper salts and chelating ligands. The latter, which have potential nitrogen‐ and/or oxygen‐binding sites, have never previously been used in this type of rea

Mild Copper-Catalyzed Vinylation Reactio
Mild Copper-Catalyzed Vinylation Reactions of Azoles and Phenols with Vinyl Bromides
✍ Marc Taillefer; Armelle Ouali; Brice Renard; Jean-Francis Spindler πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 288 KB

## Abstract An efficient and straightforward copper‐catalyzed method allowing vinylation of __N‐__ or __O‐__nucleophiles with di‐ or trisubstituted vinyl bromides is reported. The procedure is applicable to a broad range of substrates since __N‐__vinylation of mono‐, di‐, and triazoles as well as _