Synthesis of 1,4-diaminocyclitol antibiotics. I. Synthesis of 4'-hydroxyfortimicin D
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Kanai,Sakamoto,Miyamoto,et al.
p. 255 - 259
(2007/10/02)
Further Aspects of the Reduction of Dithiocarbonates with Tributyltin Hydride and Deuteride
The reduction of 1,2:5,6-di-O-isopropylidene-3-O-(methylthio)thiocarbonyl-β-D-idose, -talose, and -(3-(2H))talose with tributyltin hydride and deuteride leads to the deoxy sugar and some deuteriumcontaining deoxy sugars.A modification of the normal procedure allows for reduction with tributyltin hydride generated in situ.As well, the reduction of some dithiocarbonates derived from glycosides of N-acetyl-D-glucosamine allows to a variety of dideoxy and trideoxy sugars.
Conway, Richard J.,Nagel, Jennifer P.,Stick, Robert V.,Tilbrook, D. Matthew G.
p. 939 - 945
(2007/10/02)
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