35294-53-2Relevant academic research and scientific papers
Synthesis of the Chromophore of Pseudobactin, a Fluorescent Siderophore from Pseudomonas
Kolasa, Teodozyj,Miller, Marvin J.
, p. 4246 - 4255 (2007/10/02)
Protected forms of dihydroxyphenylalanine (DOPA) were converted to the corresponding dihydroquinolin-2-ones 13 by nitration and reductive cyclization.Subsequent N-alkylation with α-halo-γ-aminobutyric acid derivatives provided the carbon framework 12 for the chromophore of pseudobactin.Conversion to protected forms of the fluorescent chromophore 5 was accomplished by reaction of 12 with Lawesson's reagent to produce the corresponding thioamide which was cyclized by reaction with mercuric acetate.
