97389-92-9

Downstream Products

• 97389-94-1 benzyl 3-azido-2,3,6-trideoxy-α-L-threo-hex-2-enopyranoside 
• 97389-93-0 benzyl 3-azido-2,3,6-trideoxy-α-L-erythro-hex-2-enopyranoside 
• 97390-01-7 benzyl 3-acetamido-2,3,6-trideoxy-4-O-propionyl-α-L-xylo-hexopyranoside 
• 97389-96-3 benzyl 3-azido-2,3,6-trideoxy-4-O-propionyl-α-L-threo-hex-2-enopyranoside 
• 97389-95-2 benzyl 3-azido-2,3,6-trideoxy-4-O-methanesulfonyl-α-L-erythro-hex-2-enopyranoside 
• 97389-97-4 benzyl 3-acetamido-4-O-acetyl-2,3,6-trideoxy-α-L-xylo-hexopyranoside (3-epi-daunosaminide) 
• 97389-99-6 benzyl 3-acetamido-4-O-acetyl-2,3,6-trideoxy-α-L-ribo-hexopyranoside (benzyl N-acetyl-O-acetyl-α-L-ristosoaminide) 

Relevant academic research and scientific papers

SYNTHESIS AND HYDROGENATION STUDIES OF 3-AZIDOHEX-2-ENOPYRANOSIDES, PRECURSORS OF THE SUGAR CONSTITUENTS OF ANTHRACYCLINE GLYCOSIDES

Application of the allylic azide rearrangement /N-iodosuccinimide glycosylation procedure to 3,4-di-O-acetyl-L-fucal gave exclusively benzyl 4-O-acetyl-3-azido-2,3,6-trideoxy-2-iodo-α-L-idopyranoside.A similar reaction of 3,4-di-O-acetyl-L-rhamnal gave bo