Nickel-catalysed carboxylation of organoboronates was written by Makida, Yusuke;Marelli, Enrico;Slawin, Alexandra M. Z.;Nolan, Steven P.. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2014.HPLC of Formula: 1003858-50-1 The following contents are mentioned in the article:
A nickel/N-heterocyclic carbene (NHC) catalyzed carboxylation of aryl-, heteroaryl- and alkenylboronates, affording the corresponding carboxylic acids, has been developed. This transformation proceeds under one atm. of CO2 with a broad range of substrates and exhibits good functional group compatibility. This study involved multiple reactions and reactants, such as 2-(3-Methoxyphenyl)-5,5-dimethyl-1,3,2-dioxaborinane (cas: 1003858-50-1HPLC of Formula: 1003858-50-1).
2-(3-Methoxyphenyl)-5,5-dimethyl-1,3,2-dioxaborinane (cas: 1003858-50-1) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.HPLC of Formula: 1003858-50-1
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem