607724-72-1Relevant academic research and scientific papers
Lactosamine from lactulose via the Heyns rearrangement: A practical protocol
Shan, Yulong,Oulaidi, Farah,Lahmann, Martina
, p. 3960 - 3961 (2013)
The Heyns rearrangement is possibly one of the oldest, easiest and most economic ways to synthesise 2-deoxy-2-amino sugars. Initially reported yields were disappointingly low, but in the late 90s Wrodnigg and Stütz discovered modified reaction conditions
An exceptionally simple chemical synthesis of O-glycosylated D-glucosamine derivatives by Heyns rearrangement of the corresponding O-glycosyl fructoses
Stuetz, Arnold E.,Dekany, Gyula,Eder, Brigitte,Illaszewicz, Carina,Wrodnigg, Tanja M.
, p. 253 - 265 (2007/10/03)
2-N-Acetyl-4-O-(β-D-galactopyranosyl)-D-glucosamine (N-acetyl-D-lactosamine), a very important building block of biologically relevant oligosaccharides such as sialyl Lewisx, is easily accessible via the Heyns rearrangement of the corresponding
