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Palladium-Catalyzed Regiocontrolled α-Arylation of Trimethylsilyl Enol Ethers with Aryl Halides.

✍ Scribed by Tetsuo Iwama; Viresh H. Rawal

Publisher
John Wiley and Sons
Year
2007
Weight
36 KB
Volume
38
Category
Article
ISSN
0931-7597

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✦ Synopsis

Abstract

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📜 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