Alcoholic solvent-assisted ligand-free room temperature Suzuki–Miyaura cross-coupling reactionGayatri SarmahDepartment of Chemistry, Dibrugarh University, Dibrugarh, Assam, IndiaManoj MondalDepartment of Chemistry, Dibrugarh University, Dibrugarh, Assam, IndiaUtpal Bora...
Asymmetric Suzuki cross-coupling reaction: chirality reversal depending on the palladium–chiral phosphine ratio [Castanet, Anne-Sophie; Colobert, Francoise; Broutin, Pierre-Emmanuel; Obringer, Michel Tetrahedron Asymmetry, 2002 , vol. 13, # 6 p. 659 - 665] ...
Abstract Room-temperature Suzuki–Miyaura aryl–aryl cross-coupling reactions have been achieved in high yields by using an easily accessible, air-stable NiII–(σ-aryl) complex as precatalyst without either the pretreatment of organometallic reagents or the presence of external reductants. The NiII ...
S. Jadhav, A. Kumbhar, R. Salunkhe, Palladium supported on silica-chitosan hybrid material (Pd-CS@SiO2) for Suzuki-Miyaura and Mizoroki-Heck cross-coupling reactions, Appl. Organomet. Chem. 29 (2015) 339-345.S. Jadhava, A. Kumbharb, R. Salunkhe, Palladium supported on silica-chitosan ...
S. Jadhav, A. Kumbhar, R. Salunkhe, Palladium supported on silica-chitosan hybrid material (Pd-CS@SiO2) for Suzuki-Miyaura and Mizoroki-Heck cross-coupling reactions, Appl. Organomet. Chem. 29 (2015) 339-345.S. Jadhava, A. Kumbharb, R. Salunkhe, Palladium supported on silica-chitosan ...
[Google Scholar] [CrossRef] Brown, H.C.; Zaidlewicz, M. Organic Synthesis via Boranes; Aldrich: Milwaukee, WI, USA, 2001; Volume 2. [Google Scholar] Miyaura, N.; Suzuki, A. Palladium-catalyzed cross-coupling reactions of organoboron compounds. Chem. Rev. 1995, 95, 2457–2483. [...
Patra, T.; Maiti, D. Decarboxylation as the Key Step in C–C Bond-Forming Reactions.Chem. A Eur. J.2017,23, 7382. [Google Scholar] [CrossRef] [PubMed] Rodríguez, N.; Goossen, L.J. Decarboxylative coupling reactions: A modern strategy for C–C-bond formation.Chem. Soc. Rev.2011...
(WES) without using external phosphine ligand, base, and organic solvent. The cross-coupling reactions were carried out in a basic WES medium with a broad substrate scope and wide functional group tolerance. Furthermore, the high purity of solid biaryl products can be obtained by column ...