838-76-6Relevant 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
5-HYDROXY-2-METHYL-4H-PYRAN-4-ONE ESTERS AS NOVEL TYROSINASE INHIBITORS
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Page/Page column 5, (2009/09/07)
Skin brightening compositions based on esters of 5-hydroxy-2-methyl-4H-pyran-4-one. Also disclosed are methods of making the compositions as well as methods of using the compositions
Sugar Enolones, XIX. - An Approach to Actinospectose-Type 2,3-Diketo Sugars. - Synthetic Proof for the R Configuration of "Herzgift-Methylreduktinase"
Lichtenthaler, Frieder W.,Loehe, Albert,Cuny, Eckehard
, p. 1973 - 1985 (2007/10/02)
A stereochemically defined, preparatively satisfactory access is described to stable derivatives of D-actinospectose, a 4,6-dideoxy-D-glycero-hexopyranos-2,3-diulose (3a 3b) realized in spectinomycin (1) and a series of Calotropis cardenolides (2).Key
