59115-43-4Relevant articles and documents
Resorcin[4]arene-derived mono-, bis- and tetra-imidazolium salts as ligand precursors for Suzuki-Miyaura cross-coupling
El Moll, Hani,Semeril, David,Matt, Dominique,Toupet, Loic,Harrowfield, Jean-Jacques
, p. 372 - 382 (2012)
Eleven resorcinarene cavitands bearing either one, two or four (3-R-1-imidazolylium)-methyl substituents (R = nBu, Ph, Mes, iPr2C6H3) anchored at resorcinolic "ortho" positions have been synthesised f
Equilibration of the Oxidative Addition Product of Tetrakis(triphenylphosphine)palladium and Electron-Rich Aryl Halides Leads to Product Scrambling in the Stille Reaction
Segelstein, B. E.,Butler, T. W.,Chenard, B. L.
, p. 12 - 13 (1995)
-
Nickel-Catalyzed Direct Cross-Coupling of Aryl Sulfonium Salt with Aryl Bromide
Ma, Na-Na,Ren, Jing-Ao,Liu, Xiang,Chu, Xue-Qiang,Rao, Weidong,Shen, Zhi-Liang
, p. 1953 - 1957 (2022/03/27)
The direct cross-couplings of aryl sulfonium salts with aryl halides could be achieved by using nickel as a reaction catalyst. The reactions proceeded efficiently via C-S bond activation in the presence of magnesium turnings and lithium chloride in THF at ambient temperature to afford the corresponding biaryls in moderate to good yields, potentially serving as an attractive alternative to conventional cross-coupling reactions employing preprepared organometallic reagents.
Palladium complexes derived from benzoylthiourea ligands: Synthesis, crystal structure, and catalytic application in Suzuki C–C coupling reactions
Solmaz, Ummuhan,Gumus, Ilkay,Yilmaz, Mustafa Kemal,Ince, Simay,Arslan, Hakan
, (2021/07/19)
[PdCl2(HL1-κS)2] and [PdCl2(HL2-κS)2] complexes were formed from neutral monodentate modes of HL1 and HL2 ligands, which are coordinated to the palladium(II) center, r
Transition-Metal-Free Oxidative Cross-Coupling of Tetraarylborates to Biaryls Using Organic Oxidants
Gerleve, Carolin,Studer, Armido
, p. 15468 - 15473 (2020/05/06)
Readily prepared tetraarylborates undergo selective (cross)-coupling through oxidation with Bobbitt's salt to give symmetric and unsymmetric biaryls. The organic oxoammonium salt can be used either as a stoichiometric oxidant or as a catalyst in combination with in situ generated NO2 and molecular oxygen as the terminal oxidant. For selected cases, oxidative coupling is also possible with NO2/O2 without any additional nitroxide-based cocatalyst. Transition-metal-free catalytic oxidative ligand cross-coupling of tetraarylborates is unprecedented and the introduced method provides access to various biaryl and heterobiaryl systems.