Chowdari, Naidu S. published the artcileAsymmetric Synthesis of Quaternary α- and β-Amino Acids and β-Lactams via Proline-Catalyzed Mannich Reactions with Branched Aldehyde Donors, Application In Synthesis of 1205-17-0, the main research area is quaternary alpha beta amino acid lactam preparation; Mannich reaction proline catalyzed amino acid beta lactam preparation.
L-Proline-catalyzed direct asym. Mannich reactions of N-PMP protected α-imino Et glyoxylate with various α,α-disubstituted aldehydes affords quaternary β-formyl α-amino acid derivatives with excellent yields and enantioselectivities. The Mannich products are further converted to the corresponding quaternary α- and β-amino acids and β-lactams.
Organic Letters published new progress about Amino acids Role: SPN (Synthetic Preparation), PREP (Preparation). 1205-17-0 belongs to class isoquinoline, name is 2-Methyl-3-(3,4-methylenedioxyphenyl)propionaldehyde, and the molecular formula is C11H12O3, Application In Synthesis of 1205-17-0.
Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem