75414-34-5Relevant academic research and scientific papers
A convenient access to the 1,5-anhydro forms of d-tagatose, l-rhamnulose and d-xylulose via 2-hydroxyglycal esters
Jarglis, Pan,Goeckel, Volker,Lichtenthaler, Frieder W.
experimental part, p. 952 - 960 (2009/10/10)
Zemplen methanolysis or a three-step protocol comprising hydroxylaminolysis, de-O-acetylation and deoximination smoothly and efficiently convert the benzoylated 2-hydroxy-d-glycals of d-galactose, l-rhamnose and d-xylose into their configurationally relat
A CONVENIENT ACCESS TO 1,5-ANHYDROKETOSES
Lichtenthaler, F. W.,Ashry E. S. H. El,Goeckel, V. H.
, p. 1429 - 1432 (2007/10/02)
A convenient, verstile entry into the 1,5-anhydroketose series is described and their conversion into enolones, enolone oximes and γ-pyrones.
