329360-94-3

Upstream product

• 174151-46-3 benzyl 2-acetamido-2,3,4,6-tetradeoxy-α-L-threo-hex-3-enopyranoside 

Downstream Products

• 329360-99-8 benzyl 2-acetamido-3-O-acetyl-4-azido-2,4,6-trideoxy-α-L-altropyranoside 
• 329361-00-4 benzyl 2-acetamido-4-O-acetyl-3-azido-2,4,6-trideoxy-α-L-altropyranoside 
• 329360-96-5 benzyl 2-acetamido-3-azido-2,3,6-trideoxy-α-L-idopyranoside 
• 329360-95-4 benzyl 2-acetamido-4-azido-2,4,6-trideoxy-α-L-mannopyranoside 

Relevant academic research and scientific papers

Observations on the oxirane ring opening reactions of a 2-acetamido-3,4-anhydro sugar and on the inversion of the derived alcohols

A novel methodology for the preparation of L-enantiomers of 2,4- and 2,3-diacetamido-2,4,6- and 2,3,6-trideoxy-pyranoses is described. Factors influencing both the steric course of the epoxide ring opening and substitution are discussed.