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ChemInform Abstract: Arylation of Phosphoryl-Stabilized Carbanions with Metal π-Complexes of Aryl Chlorides and Fluorides.

✍ Scribed by Galina A. Artamkina; Petr K. Sazonov; Irina P. Beletskaya

Publisher
John Wiley and Sons
Year
2010
Weight
34 KB
Volume
32
Category
Article
ISSN
0931-7597

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

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