Description

• Application: 4-Cyanophenylboronic acid can be used as a reactant in:Palladium-catalyzed Suzuki-Miyaura cross-coupling in water.[1]Ruthenium catalyzed direct arylation of benzylic sp3 carbons of acyclic amines with arylboronates.[2]Ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids.[3]Ferric perchlorate-promoted reaction of fullerenes with various arylboronic acids to give fullerenyl boronic esters.[4]Phosphine-free Suzuki-Miyaura cross-coupling.[5]Palladacycles as effective catalysts for multicomponent reaction with allylpalladium-intermediates.[6]Chan-Lam-type Cu-catalyzed S-arylation of thiols.[7] Regioselective cross-coupling reactions under modfied Suzuki and Still cross-coupling reactions with copper catalysis.[8]Metal-free biaryl coupling reaction in the presence of dimethyl carbonate as a solvent.[9]Suzuki-type cross-coupling reaction with pentavalent triarylantimony diacetates in the absence of a base.[10]It can also be used to prepare:Himbacine analogs as thrombin receptor antagonists and potential antiplatelet agents.[11]Trisulfonated calixarene upper-rim sulfonamido and their complexation with trimethyllysine epigenetic mark.[12]Antimalarial compounds via Suzuki cross-coupling.[13]Deoxyuridine derivatives.[1]
• Other Notes: Contains varying amounts of anhydride