147221-45-2

Downstream Products

• 147221-46-3 methyl 4,6-O-benzylidene-3-tert-butoxycarbonylamino-3-C-cyano-2,3-dideoxy-α-D-arabino-hexopyranoside 
• 147221-51-0 methyl 4-O-benzoyl-6-bromo-3-tert-butoxycarbonylamino-3-C-tert-butoxycarbonylaminomethyl-2,3,6-trideoxy-α-D-arabino-hexopyranoside 
• 147221-52-1 methyl 4-O-benzoyl-3-C-tert-butoxycarbonylaminomethyl-3,6-(N-tert-butoxycarbonyl)imino-2,3,6-trideoxy-α-D-arabino-hexopyranoside 
• 147221-50-9 methyl 4,6-O-benzylidene-3-tert-butoxycarbonylamino-3-C-tert-butoxycarbonylaminomethyl-2,3-dideoxy-α-D-arabino-hexopyranoside 

Relevant academic research and scientific papers

Synthesis of some further C-3 branched 3-amino-2,3,6-trideoxy sugars, related to daunosamine, as potential components for structurally modified anthracyclines

A Hofmann-type, oxidative rearrangement of methyl 4,6-O-benzylidene-3-C-carbamoyl-3-C-cyano-3-deoxy-α-D-glucopyranoside (1) by mercuric acetate and N-bromosuccinimide resulted in a 2-oxazolidinone ring fused to the pyranoside. Deoxygenation by tributylsta