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Ag(I)-promoted Suzuki–Miyaura cross-couplings of n-alkylboronic acids

✍ Scribed by Gang Zou; Y.Krishna Reddy; J.R. Falck

Book ID
104231585
Publisher
Elsevier Science
Year
2001
Tongue
French
Weight
59 KB
Volume
42
Category
Article
ISSN
0040-4039

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✦ Synopsis

Ag(I) salts significantly enhance palladium-catalyzed Suzuki-Miyaura cross-couplings of n-alkylboronic acids with a wide variety of aryl and alkenyl halides/triflates.

📜 SIMILAR VOLUMES

Suzuki–Miyaura Cross-Coupling Reactions
Suzuki–Miyaura Cross-Coupling Reactions of Alkylboronic Acid Derivatives or Alkyltrifluoroborates with Aryl, Alkenyl or Alkyl Halides and Triflates
✍ Henri Doucet 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 592 KB

## Abstract Palladium‐catalysed Suzuki–Miyaura cross‐couplings of organoboronic acids or organotrifluoroborates with aryl and alkenyl halides or triflates have become classic methods for generating carbon–carbon bonds. For this reaction, not only sp^2^‐hybridized but also sp^3^‐hybridized organobor