210832-86-3Relevant articles and documents
Enantioselective synthesis and application of the highly fluorescent and environment-sensitive amino acid 6-(2-dimethylaminonaphthoyl) alanine (DANA).
Nitz, Mark,Mezo, Adam R,Ali, Mayssam H,Imperiali, Barbara
, p. 1912 - 1913 (2002)
6-(2-Dimethylaminonaphthoyl) alanine (DANA) was prepared via an enantioselective synthesis and incorporated into the S-peptide of RNase S establishing the large changes in fluorescence that can occur upon peptide-protein interaction.
A facile protocol for the convenient preparation of amino-substituted α-bromo- and α,α-dibromo arylmethylketones
Diwu, Zhenjun,Beachdel, Christopher,Klaubert, Dieter H.
, p. 4987 - 4990 (2007/10/03)
Amino-substituted arylmethylketones are selectively brominated in sulfuric acid to afford the corresponding dibromomethylarylketones that are then debrominated with diethylphosphite to give the desired bromomethylarylketones in excellent yield.