1311277-70-9

Upstream product

• 1311277-66-3 2,6-anhydro-1,3,5-tri-O-benzyl-4-O-(3-O-benzyl-1,2-O-isopropylidene-α-D-ribofuranosuronyl)-7,8,9-trideoxy-D-glycero-D-manno-non-8-enitol 
• 1311277-67-4 3,7-anhydro-4,6,8-tri-O-benzyl-5-O-(3-O-benzyl-1,2-O-isopropylidene-α-D-ribofuranosuronyl)-2-deoxy-D-glycero-α-D-talo-octonic acid 
• 1311277-68-5 3,7-anhydro-4,6,8-tri-O-benzyl-5-O-(3-O-benzyl-1,2-O-isopropylidene-α-D-ribofuranosuronyl)-2-deoxy-D-glycero-α-D-talo-octonyl chloride 
• 1311277-69-6 3,7-anhydro-N-(2-amino-6-benzyloxy-5-nitrosopyrimidin-4-yl)-4,6,8-tri-O-benzyl-5-O-(3-O-benzyl-1,2-O-isopropylidene-α-D-ribofuranosuronyl)-2-deoxy-D-glycero-D-talo-octonamide 
• 617-04-9 (2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3,4,5-triol 
• 187152-84-7 methyl 2,4,6-tri-O-benzyl-3-O-(4-methoxybenzyl)-α-D-mannopyranoside 
• 120417-90-5 1,2-O-(methylethylidene)-3-O-(phenylmethyl)-α-D-ribofuranuroic acid 
• 100-39-0 benzyl bromide 
• 63593-02-2 3-O-benzyl-1,2-O-isopropylidene-α-D-ribo-pentodialdo-1,4-furanose 
• 1311277-65-2 2,6-anhydro-1,3,5-tri-O-benzyl-7,8,9-trideoxy-D-glycero-D-manno-non-8-enitol 

Relevant academic research and scientific papers

Towards stable di-carba analogues of guanofosfocins

Guanofosfocins are strong inhibitors of chitin synthases, but also very prone to hydrolytic cleavage. Two advanced intermediates 15 and 20 for the synthesis of stable di-carba-guanofosfocins were prepared via ester 11. Acylation of the allylic C-glycoside