100102-49-6

Upstream product

• 100164-72-5 Methyl-3,4,6-tridesoxy-α-D-erythro-hex-3-enopyranosid 
• 63902-64-7 Methyl-3,4,6-tridesoxy-β-D-erythro-hex-3-enopyranosid 
• 61135-30-6 Methyl-3,4,6-tridesoxy-β-D-glycero-hex-3-enopyranosid-2-ulose 
• 142632-74-4 methyl 4,6-O-benzylidene-2,3-dideoxy-β-D-erythro-hexopyranoside 
• 65530-31-6 (4aR,6R,8aS)-6-methoxy-2-(4-methoxyphenyl)-4,4a,6,8a-tetrahydropyrano[3,2-d][1,3]dioxine 
• 142573-09-9 methyl 4-O-benzoyl-6-bromo-2,3,6-trideoxy-β-D-erythro-hexopyranoside 
• 100102-48-5 Methyl-4-O-benzoyl-3,4,6-tridesoxy-β-D-erythro-hex-2-enopyranosid 

Downstream Products

• 142573-13-5 methyl 4-O-<3,4-O-benzylidene-2-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-α-L-arabinopyranosyl>-2,3,6-trideoxy-β-D-erythro-hexopyranoside 
• 142573-12-4 methyl 4-O-(3,4-O-benzylidene-α-L-arabinopyranosyl)-2,3,6-trideoxy-β-D-erythro-hexopyranoside 

Relevant academic research and scientific papers

Molecular recognition XI. The synthesis of extensively deoxygenated derivatives of the H-type 2 human blood group determinant and their binding by an anti-H-type 2 monoclonal antibody and the lectin 1 of Ulex europaeus

The relative potencies of a wide variety of deoxygenated derivatives of the methyl glycoside of α-L-Fuc-(1->2)-β-D-Gal-(1->4)-β-D-GlcNAc (the H-type 2 human blood related trisaccharide) for the inhibition of the binding of an artificial H-type 2 antigen b

Syntheses of Biologically Important Carbohydrates, 33. - Syntheses of Unsaturated Amino Sugars and Aminoalkyl-branched Carbohydrates via Sigmatropic Rearrangement of Trichloroacetimidates

Starting with the α-D-erythro-hex-3-enopyranoside 1 the isomers with β-D-erythro as well as α- and β-D-threo configuration 5b, 3b, and 9 are prepared.In Mitsunobu reactions the 1,2-cis derivatives 1 and 9 smoothly undergo SN2-type substitutions