𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Pd-Catalyzed α-Arylation of α,α-Difluoroketones with Aryl Bromides and Chlorides. A Route to Difluoromethylarenes

✍ Scribed by Ge, Shaozhong; Chaładaj, Wojciech; Hartwig, John F.

Book ID
124084910
Publisher
American Chemical Society
Year
2014
Tongue
English
Weight
392 KB
Volume
136
Category
Article
ISSN
0002-7863

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Pd-Catalyzed α-Arylation of Trimethylsil
Pd-Catalyzed α-Arylation of Trimethylsilyl Enol Ethers with Aryl Bromides and Chlorides: A Synergistic Effect of Two Metal Fluorides as Additives
✍ Weiping Su; Steven Raders; John G. Verkade; Xuebin Liao; John F. Hartwig 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 127 KB 👁 1 views

Ketone enolates are among the most common nucleophiles in organic chemistry, and transition-metal-catalyzed cross-coup ling reactions are among the most commonly used catalytic processes. [1] However, the combination of these two chemistries-cross-coupling of enolate nucleophiles-has been developed

Pd-Catalyzed α-Arylation of Trimethylsil
Pd-Catalyzed α-Arylation of Trimethylsilyl Enol Ethers with Aryl Bromides and Chlorides: A Synergistic Effect of Two Metal Fluorides as Additives
✍ Weiping Su; Steven Raders; John G. Verkade; Xuebin Liao; John F. Hartwig 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 127 KB 👁 1 views

Ketone enolates are among the most common nucleophiles in organic chemistry, and transition-metal-catalyzed cross-coup ling reactions are among the most commonly used catalytic processes. [1] However, the combination of these two chemistries-cross-coupling of enolate nucleophiles-has been developed