Methylboronic acid

Chemical Properties

Uses

• In the palladium-catalyzed Stille and Suzuki-Miyaura cross-couplings.
• In the microwave-heated heterogeneous palladium (Pd)-catalytized reactions.
• In ruthenium (Ru)-catalyzed silylation reactions
• To prepare bis(aminotropone) titanium (Ti) catalysts for ethylene polymerizations.
• In the enantioselective asymmetric bromoaminocyclization and bromoaminocyclization using amino-thiocarbamate catalysts.
• To prepare common building blocks for pharmaceuticals and agrochemicals.
• To prepare chrysin analogs by Suzuki-Miyaura coupling reactions.
• To prepare casein kinase I inhibitors.
• In the divergent C-H functionalizations directed by sulfonamide pharmacophores in drug discovery.
• In the synthesis of unsymmetrical monosulfides from disulfides via copper-catalyzed coupling with boronic acids.
• In a palladium-catalyzed coupling with enol tosylates.
• For derivatizing many carbohydrates and biologically active compounds for GLC analysis.

Uses

Uses