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Synthesis of biaryls via nickel-catalyzed cross-coupling reaction of arylboronic acids and aryl mesylates

โœ Scribed by Masato Ueda; Atsushi Saitoh; Saori Oh-tani; Norio Miyaura


Book ID
104208876
Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
407 KB
Volume
54
Category
Article
ISSN
0040-4020

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โœฆ Synopsis


The cross-coupling reaction of arylboronic acids (1.3 equivs) with aryl methanesulfonates was carded out in the presence of anickel(O) catalyst(3 tool%) and K3PO~,nH20 (3 equivs). The use of toluene as the solvent and the nickel(O)-dppf catalyst prepared from NiC~(dppf) plus dppf with BuLi were recognized to be the most efficient to achieve both high yields and high selectivity. The reaction can be app~ed to various electron-deficient and -rich aryl methanesulfonates to give high yields.


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ChemInform Abstract: Synthesis of Biaryl
โœ S. SAITO; S. OH-TANI; N. MIYAURA ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 41 KB ๐Ÿ‘ 1 views

Synthesis of Biaryls via a Nickel(0)-Catalyzed Cross-Coupling Reaction of Chloroarenes with Arylboronic Acids. -Optimized conditions are found for coupling of a wide range of chloroarenes with various functionalized arylboronic acids using K 3 PO 4 as base and dioxane or benzene as solvent. Nickel(0