53434-69-8

Upstream product

• 6167-32-4 1,6:3,4-dianhydro-2-O-tosyl-D-galactose 

Downstream Products

• 55639-81-1 1,6-anhydro-4-deoxy-4-iodo-2-O-p-toluenesulfonyl-β-D-galactopyranose 
• 279-17-4 1,6:2,3-dianhydro-4-deoxy-β-D-lyxo-hexopyranose 
• 88146-17-2 1,6-anhydro-3-O-(N-benzylcarbamoyl)-4-deoxy-2-O-p-toluensulfonyl-β-D-xylo-hexopyranose 
• 88146-18-3 3-benzyl-(1,6-anhydro-2,3,4-trideoxy-β-D-lyxo-hexopyrano)-<2,3-d>-oxazolidin-2-one 
• 88146-19-4 1,6-anhydro-2-benzylamino-2,4-dideoxy-β-D-lyxo-hexopyranose 
• 95628-49-2 3-O-acetyl-1,6-anhydro-4-deoxy-2-O-tosyl-β-D-xylopyranose 

Relevant academic research and scientific papers

PREPARATION OF 2-AMINO-2,4-DIDEOXY-D-lyxo-HEXOPYRANOSE (4-DEOXY-D-MANNOSAMINE) FROM 1,6-ANHYDRO-β-D-GLUCOPYRANOSE

1,6-Anhydro-4-deoxy-2-O-p-toluenesulfonyl-β-D-xylo-hexopyranose (III), obtainable by a four-step synthesis from 1,6-anhydro-β-D-glucopyranose, was converted to 3-O-(N-benzylcarbamoyl) derivative V on reaction with benzyl isocyanate.The cyclization of V wi

Bausteine von Oligosacchariden, XXI. Synthesen von Gentamicin X2 und am C-4' und C-3' modifizierter Gentamicine

The garamine derivative 18 can be coupled with the β-chloride 15 of 2-azido-2-deoxy-D-glucose to 20 from which, by deblocking procedure, gentamicin X2 (23) is available.In the same manner the 4'-amino- and 4'-chloro compound 24 and 25, resp., can be obtained.Coupling of 26 with 19 gives the product 27 from which the derivative 28 of gentamicin, modified at C-3', is prepared.