Room??Temperature Synthesis of Tetra??ortho??Substituted Biaryls by NHC??Catalyzed Suzuki–Miyaura Couplings

…, S Capolicchio, A Linden, L Falivene…

Index: Wu, Linglin; Drinkel, Emma; Gaggia, Fiona; Capolicchio, Samanta; Linden, Anthony; Falivene, Laura; Cavallo, Luigi; Dorta, Reto Chemistry - A European Journal, 2011 , vol. 17, # 46 p. 12886 - 12890

Full Text: HTML

Citation Number: 53

Abstract

Transition-metal-catalyzed cross couplings have become some of the most powerful and widely used methods to construct CÀC bonds.[1] Among them, the Suzuki–Miyaura coupling,[2] has emerged as a particularly attractive and practical tool for synthetic organic chemistry.[3] Indeed, over the last decade, several limitations of this methodology have been successfully addressed by using bulky, electron-rich monodentate phosphines or ...

Related Articles:

Halogenation Using Quaternary Ammonium Polyhalides. XIX. Aromatic Chlorination of Arenes with Benzyltrimethylammonium Tetrachloroiodate

[Kajigaeshi, Shoji; Ueda, Yasuhiro; Fujisaki, Shizuo; Kakinami, Takaaki Bulletin of the Chemical Society of Japan, 1989 , vol. 62, # 6 p. 2096 - 2098]

Microwave assisted solid additive effects in simple dry chlorination reactions with n-chlorosuccinimide

[Bucos, Madalina; Villalonga-Barber, Carolina; Micha-Screttas, Maria; Steele, Barry R.; Screttas, Constantinos G.; Heropoulos, Georgios A. Tetrahedron, 2010 , vol. 66, # 11 p. 2061 - 2065]

Alkyl nitrite-metal halide deamination reactions. 2. Substitutive deamination of arylamines by alkyl nitrites and copper (II) halides. A direct and remarkably efficient …

[Doyle,M.P. et al. Journal of Organic Chemistry, 1977 , vol. 42, p. 2426 - 2431]

More Articles...