120417-90-5

Upstream product

• 63593-02-2 3-O-benzyl-1,2-O-isopropylidene-α-D-ribo-pentodialdo-1,4-furanose 

Downstream Products

• 121611-66-3 (3R,4R)-4-Benzyloxy-tetrahydro-furan-2,3-diol 
• 121611-68-5 (2S,3S)-2-Benzyloxy-pent-4-ene-1,3-diol 
• 76768-64-4 (3aR,6R,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole 
• 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 
• 1311277-70-9 2,6-anhydro-1,3,5-tri-O-benzyl-7-(O6-benzylguanin-8-yl)-5-O-(3-O-benzyl-1,2-O-isopropylidene-α-D-ribofuranosuronyl)-7-deoxy-D-glycero-D-manno-heptitol 
• 1311277-71-0 C₄₅H₅₂O₁₂ 
• 1311277-72-1 C₄₈H₅₆O₁₂ 
• 1311277-73-2 C₄₉H₅₈O₁₁ 
• 1311277-74-3 C₄₉H₆₀O₁₂ 
• 1311277-75-4 C₅₁H₆₂O₁₃ 
• 1311277-76-5 C₄₇H₅₄O₁₃ 
• 111611-84-8 (4S)-4-<(1R,2R)-1-(phenylmethoxy)-2-(benzoyloxy)-4-penten-1-yl>-2,2-dimethyl-1,3-dioxole 

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

New Chirons from D-Glucose. Regio- and Diastereoselective C-C Bond Forming Reactions Exploiting Novel Aldotetrafuranose Acetates as Chiral Synthetic Equivalents of Tartaric Aldehydes

Two differentially protected tetrafuranose acetates 5 and 6 have been prepared from diacetone D-glucose in parallel short routes.They clearly act as chiral synthetic equivalents of D- and meso-tartaric aldehydes when exploited in Lewis acid promoted react

NOVEL SYNTHETIC EQUIVALENTS OF DIFFERENTIALLY PROTECTED TARTARIC ALDEHYDES. A SIMPLE ROUTE TO USEFUL C-4 CHIRAL SYNTHONS.

The synthesis of 4-acetoxy-3-O-benzyl-1,2-O-isopropylidene aldotetroses from D-glucose is reported.These synthetic equivalents of tartaric aldehydes are chemoselectively reduced at the acetoxylated center leading to a series of useful differentially protected C-4 chiral synthons.