Gao, Guangpeng published the artcileEnantiomeric discrimination of α-hydroxy acids and N-Ts-α-amino acids by 1H NMR spectroscopy, Category: bromides-buliding-blocks, the main research area is hydroxy acid enantiomeric discrimination proton NMR spectroscopy; protected amino acid enantiomeric discrimination proton NMR spectroscopy; chiral solvating agent amino amido phenolic hydroxy group containing.
A new kind of chiral compounds with multiple amino, amido and phenolic hydroxy groups was synthesized from D-phenylalanine and D-phenylglycine, resp. The enantiomeric discriminations of α-hydroxy acids and N-Ts-α-amino acids were finished in the presence of the above chiral compounds as chiral solvating agents by 1H NMR spectroscopy. The chiral compounds are highly effective and practical chiral solvating agents towards α-hydroxy acids and N-Ts-α-amino acids.
Tetrahedron Letters published new progress about Amino acids, N-protected Role: ANT (Analyte), ANST (Analytical Study). 156089-67-7 belongs to class bromides-buliding-blocks, name is 4,5-Dibromo-2-hydroxybenzaldehyde, and the molecular formula is C7H4Br2O2, Category: bromides-buliding-blocks.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary