732296-48-9

Upstream product

• 1554004-75-9 benzyl 7-O-tetra-butyldiphenylsilyl-2,3,4-O-tri-benzyl-D-glycero-α-D-mannoheptopyranoside 
• 106445-56-1 benzyl 2,3,4-tri-O-benzyl-α-D-glycero-D-manno-heptopyranoside 
• 1554004-68-0 benzyl 2,3,4-O-tribenzyl-6,7-dideoxy-α-D-hept-6-enopyranoside 
• 57783-76-3 benzyl 2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 1222709-77-4 benzyl 6-O-tetra-butyldiphenylsilyl-2,3,4-O-tribenzyl-α-D-mannopyranoside 
• 100-39-0 benzyl bromide 
• 114894-82-5 benzyl 6-O-tetra-butyldiphenylsilyl-α-D-mannopyranoside 
• 15548-45-5 (2S,3S,4S,5S,6R)-2-benzyloxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol 
• 530-26-7 D-Mannose 
• 1588523-50-5 C₅₈H₅₉NO₁₀Si 
• 102046-36-6 (2S,3S,4S,5S,6S)-3,4,5,6-tetrabenzyloxytetrahydropyran-2-carbaldehyde 
• 1554004-89-5 benzyl 7-O-tetra-butyldiphenylsilyl-2,3,4-O-tri-benzyl-L-glycero-α-D-mannoheptopyranoside 
• 732296-47-8 Acetic acid (2R,3R,4S,5S,6S)-4,5-diacetoxy-6-benzyloxy-2-((S)-1,2-diacetoxy-ethyl)-tetrahydro-pyran-3-yl ester 
• 100-51-6 benzyl alcohol 

Downstream Products

• 1554004-95-3 benzyl 7-O-dibenzyl-phosphono-2,3,4,6-O-tetra-benzyl-L-glycero-α-D-mannoheptopyranoside 
• 732296-49-0 benzyl-7-O-(3,4,6-tri-O-acetyl-2-N-allyloxycarbonyl-2-amino-2-deoxy-β-D-glucopyranosyl)-2,3,4,6-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranoside 
• 111570-49-1 benzyl 2,3,4,6-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranoside 

Relevant academic research and scientific papers

Chemoenzymatic synthesis of ADP-d-glycero-β-d-manno-heptose and study of the substrate specificity of HldE

An efficient one-pot three enzymes strategy for chemoenzymatic synthesis of ADP-d-glycero-β-d-manno-heptose (ADP-d, d-heptose) was reported using chemically synthesized d, d-heptose-7-phosphate and the ADP-d, d-heptose biosynthetic enzymes HldE and GmhB M

Novel synthesis of disaccharides containing the 2-amino-2-deoxy-β-D- glucopyranosyl unit and L-Glycero-D-Manno- and 7-deoxy-L-Glycero-D-Galacto- heptopyranoses

Stereocontrolled syntheses of immunologically relevant heptopyranose disaccharides were achieved in excellent yields by the trimethylsilyl triflate promoted glycosylation of the donor 1,3,4,6-tetra-O-acetyl-2-N-allyloxycarbonyl- 2-amino-2-deoxy-β-D-glucop