107908-97-4Relevant academic research and scientific papers
Novel and convenient method for the syntheses of 2,6-dideoxypyranoses, 3,6-dideoxypyranoses, and azido (amino) analogs of 3,6-dideoxypyranoses
Chang, Cheng-Wei Tom,Clark, Terri,Ngaara, Mumbi
, p. 6797 - 6801 (2007/10/03)
A novel method of regioselective deoxygenation of methyl 4,6-O-benzylidene-2,3-di-O-tosyl-α-D-glucopyranoside, and its application for the syntheses of 2,6-dideoxypyranoses, 3,6-dideoxypyranoses, and azido (amino) analogs of 3,6-dideoxypyranoses were reported.
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.
Investigation of Different Synthetic Approaches towards Methyl 2,6-Dideoxy-α-D-arabino- and -α-D-lyxo-hexopyranosides
Kjoelberg, Ove,Neumann, Klaus
, p. 721 - 727 (2007/10/02)
New synthetic routes for making available different methyl 2,6-dideoxyhexopyranosides are reported.Starting with methyl 6-deoxy-2,3-O-isopropylidene-α-D-manno- and -α-D-talo-pyranoside the respective methyl 2,6-dideoxy-α-D-arabino- and α-D-lyxo-hexopyrano
A Highly Stereoselective Synthesis of the AB Disaccharide Unit of Olivomycin A
Roush, William R.,Lin, Xiaofa,Straub, Julie A.
, p. 1649 - 1655 (2007/10/02)
A highly stereoselective synthesis of the AB disaccharide (4c) of olivomycin A is described.The synthesis features the double asymmetric allylboration of α,β-dialkoxy aldehyde 8 using tartrate allylboronate (S,S)-9, which provides triol derivative 10 with
