Simagchem Corp.

Uses suzuki reaction

Uses 4-Formylbenzeneboronic acid acts as a reagent used for Palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water, copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides, ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids, triethylamine-catalyzed three-component Hantzsch condensations, copper-catalyzed nitrations, oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta, palladacycle-catalyzed cross-coupling of arylboronic acids with carboxylic anhydrides or acyl chlorides, palladium-catalyzed aerobic oxidative cross-coupling reactions. It acts as a reagent used in preparation of sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells, a novel protein synthesis inhibitor active against Gram-positive bacteria.

Uses

4-Formylphenylboronic acid is a substrate for Suzuki cross-coupling reactions and it can be used as a reagent for:

Palladium-catalyzed Suzuki-Miyaura cross-coupling in water.

Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides.

Ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids.

Triethylamine-catalyzed three-component Hantzsch condensations.

Copper-catalyzed nitrations.

Oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta.

Palladacycle-catalyzed cross-coupling of arylboronic acids with carboxylic anhydrides or acyl chlorides.

Palladium-catalyzed aerobic oxidative cross-coupling reactions.

The synthesis of sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells.

The synthesis of a novel protein synthesis inhibitor active against Gram-positive bacteria.

The Suzuki aryl-aryl coupling of the upper rim of hexahomotrioxacalix[3]arene.

A rhodium-catalyzed cyclization, converting 1,5-enynes to cyclopentenes and spiro-cyclopentenes.