363619-65-2

Upstream product

• 4163-65-9 per-O-acetyl-α-D-mannopyranose 
• 170998-34-2 Allyl 4,6-di-O-benzyl-2,3-O-isopropylidene-α-D-mannopyranoside 
• 119111-31-8 allyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside 
• 85207-15-4 allyl 2,3:4,6-di-O-isopropylidene-α-D-mannopyranoside 
• 85207-16-5 allyl 2,3-O-isopropylidene-α-D-mannopyranoside 
• 357604-61-6 2,3:4,6-di-O-isopropylidene-D-mannopyranose 
• 41308-76-3 allyl α-D-mannopyranoside 
• 4132-28-9 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside 
• 98-88-4 benzoyl chloride 
• 363619-54-9 ((3aS,4S,6R,7R,7aS)-7-Benzyloxy-6-benzyloxymethyl-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-ylmethyl)-phosphonic acid dimethyl ester 
• 363619-53-8 ((3aS,4R,5aR,9aR,9bS)-2,2,8,8-Tetramethyl-hexahydro-[1,3]dioxolo[4',5':4,5]pyrano[3,2-d][1,3]dioxin-4-ylmethyl)-phosphonic acid dimethyl ester 

Downstream Products

• 493013-07-3 C₆₈H₆₇O₂₀PSi 
• 493012-86-5 C₆₅H₅₅Cl₃NO₂₀P 
• 493012-75-2 C₆₇H₆₅O₂₀PSi 
• 493012-74-1 C₃₅H₃₁O₁₂P 

Relevant academic research and scientific papers

Synthesis of β-D-Galp-(1 →4)-α-D-Manp methanephosphonate, a substrate analogue for the elongating α-D-mannosyl phosphate transferase in the Leishmania

An isosteric C-glycoside phosphono analogue of dec-9-enyl β-D-galactopyranosyl-(1 →4)-α-D-mannopyranosyl phosphate was synthesised and showed high biological activity in the Leishmania MPT assay. A one-step Horner-Emmons/Michael reaction was developed for the stereoselective preparation of α-D-mannosyl methanephosphonate derivatives.