Murakami, Hiroki published the artcileNovel Aza-Michael Addition-Asymmetric Protonation to α,β-Unsaturated Carboxylic Acids with Chiral Thiourea-Boronic Acid Hybrid Catalysts, Synthetic Route of 104-01-8, the main research area is propenoic acid hydroxylamine chiral thiourea tandem aza Michael protonation; hydroxyamino propanoic acid preparation enantioselective.
In this study, an efficient method was developed for controlling carbonyl α-chirality with functionalizing β-position by the conjugate addition-asym. protonation (CAAP) of α,β-unsaturated carboxylic acids using chiral thiourea-amino boronic acid hybrid catalysts. In addition, the method was applied to the asym. synthesis of biol. active compounds
Asian Journal of Organic Chemistry published new progress about Aliphatic amino acids Role: SPN (Synthetic Preparation), PREP (Preparation). 104-01-8 belongs to class isoquinoline, name is 4-Methoxyphenylacetic acid, and the molecular formula is C9H10O3, Synthetic Route of 104-01-8.
Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem