75414-19-6Relevant 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
SELECTIVE DEACYLATION OF ENOL ESTERS WITH HYDROXYLAMINE
Lichtenthaler, Frieder W.,Jarglis, Pan
, p. 1425 - 1428 (2007/10/02)
An effective procedure for selectively cleaving enol esters in the presence of normal ester functions has been developed, involving hydroxylaminolysis to the oxime of the parent ketone.
