Authors Morisawa, T; Sawamura, M; Shimizu, Y in AMER CHEMICAL SOC published article about ELECTROPHILIC AMINATION; ASYMMETRIC-SYNTHESIS; ENANTIOSELECTIVE AMINATION; DERIVATIVES; ACETALS; ESTERS; CYANOACETATES; CONSTRUCTION; COMPLEXES; STRATEGY in [Sawamura, Masaya; Shimizu, Yohei] Hokkaido Univ, Inst Chem React Design & Discovery WPI ICReDD, Kita Ku, Kita 21 Nishi 10, Sapporo, Hokkaido 0010021, Japan; [Morisawa, Takuto; Sawamura, Masaya; Shimizu, Yohei] Hokkaido Univ, Fac Sci, Dept Chem, Kita Ku, Kita 10 Nishi 8, Sapporo, Hokkaido 0600810, Japan in 2019, Cited 45. COA of Formula: C10H12O2. The Name is 2-Phenylbutanoic acid. Through research, I have a further understanding and discovery of 90-27-7
A boron-catalyzed alpha-amination of simple carboxylic acids was developed. Catalytically generated boron enolates of carboxylic acids reacted with an electrophilic aminating reagent, diisopropylazodicarboxylate, to provide amino acid derivatives. The catalysis afforded not only alpha-monosubstituted glycine derivatives but also alpha,alpha-disubstituted derivatives. The resulting alpha-aminocarboxylic acid was easily converted to carboxylic acid derivatives. Extension to a catalytic asymmetric variant was possible by introducing a chiral ligand on the boron catalyst.
COA of Formula: C10H12O2. About 2-Phenylbutanoic acid, If you have any questions, you can contact Morisawa, T; Sawamura, M; Shimizu, Y or concate me.
Reference:
Benzisoxazole – Wikipedia,
,Benzisoxazole – an overview | ScienceDirect Topics