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...
Click ionic liquids:A family of promising tunable solvents and application in Suzuki-Miyaura cross-coupling. Li L,Wang J,Wu T,Wang R. Chemistry A European Journal . 2012Li,L.Y,Wang,J.Y,Wu,T,Wang,R.H.Click ionic liquids:a family of promising tunable solvents and application in Suzuki-...
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] ...
cross-couplingnanoparticlespalladiumphosphorusJeanneL. Bolliger, ChristianM. Frech DrChemistry - A European JournalDichloro-Bis(aminophosphine) Complexes of Palladium:Highly Convenient, Reliable and Extremely Active Suzuki-Miyaura Catalysts with Excellent Functional Group Tolerance. BOLLIGER J L,FRECH C M. ...
Carson, F.; Pascanu, V.; Bermejo Gomez, A.; Zhang, Y.; Platero-Prats, A.E.; Zou, X.; Martin-Matute, B. Influence of the Base on Pd@MIL-101-NH2(Cr) as Catalyst for the Suzuki-Miyaura Cross-Coupling Reaction. Chem. A Eur. J. 2015, 21, 10896-10902. [CrossRef]...
Cross-couplingAn efficient method for the construction of two distinct C aryl –C aryl bonds through the Ni-catalyzed Suzuki–Miyaura cross-coupling of phenols with arylboronic acids has been developed. This reaction proceeds through the in situ tosylation of phenols by using N , N -ditosyl...
doi:10.1002/chin.201314149Davey, Paul R. J.Delouvrie, BenedicteDorison-Duval, DelphineGermain, HerveHarris, Craig S.Magnien, FrancoiseOuvry, GillesTricotet, ThomasWILEY‐VCH VerlagCheminform
Cross-couplingC–C couplingPalladiumBiarylsN ligandsWe report a new catalyst system, a morpholine–Pd(OAc) 2 complex, for Suzuki–Miyaura coupling of aryl tosylates or mesylates with arylboronic acids to give biaryl compounds. The morpholine–Pd(OAc) 2 catalyst system is proposed to be a ...
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 ...
doi:10.1002/slct.201600537cellulosecorn-cobpoly(amidoximepalladium nanoparticlesSuzuki-MiyauraSultana, TMandal, Bablu HiraRahman, Md. LutforSarkar, Shaheen MChemistryselect