74524-02-0Relevant articles and documents
Studies of the stereoselective reduction of ketosugar (hexosulose)
Chang, Cheng-Wei Tom,Hui, Yu,Elchert, Bryan
, p. 7019 - 7023 (2007/10/03)
The results from the studies of the stereoselective reduction of ketosugar (hexosulose) were reported. Combining our results and those reported in the literature, we summarize the factors in controlling the stereoselective reduction of ketosugars. These findings are valuable in the synthesis of various carbohydrate derivatives.
Ulose formation by selenoxide elimination
Heath, Christine E.,Gillam, Maria C.,Callis, Carrie S.,Patto, Robert R.,Abelt, Christopher J.
, p. 371 - 373 (2007/10/03)
Ring opening of methyl 2,3-anhydro-(R)-4,6-O-benzylidene-α-D- mannopyranoside with phenyl selenide gives (R)-4,6-O-benzylidene-3-Se- phenyl-3-seleno-α-D-altropyranoside (2). Oxidation of (2) with H2O2 followed by thermolysis gives methyl (R)-4,6-O-benzylidene-3-deoxy-α-D- erythrohexopyranosid-2-ulose via syn-elimination and ketoenol tautomerization.