N-Boc-2-pyrroleboronic acid serves as a valuable biochemical reagent targeting organic synthesis applications. Its boronic acid functional group allows for participation in Suzuki coupling reactions, facilitating the construction of chiral pharmaceutical and biologically active compounds. Additionally, the oxidizable boronic acid can convert to a hydroxyl group in the presence of nitrogen oxides, leading to further transformation into 2-oxo-2,5-dihydro-1-pyrrolecarboxylic acid tert-butyl ester through tautomerization.
N-Boc-2-pyrroleboronic acid serves as a valuable biochemical reagent targeting organic synthesis applications. Its boronic acid functional group allows for participation in Suzuki coupling reactions, facilitating the construction of chiral pharmaceutical and biologically active compounds. Additionally, the oxidizable boronic acid can convert to a hydroxyl group in the presence of nitrogen oxides, leading to further transformation into 2-oxo-2,5-dihydro-1-pyrrolecarboxylic acid tert-butyl ester through tautomerization.
This calculator helps you calculate mass of compound based on solution concentration, volume and molecular weight in a specific solution using the formula:
