117399-36-7

Upstream product

• 32469-90-2 methyl 3,4-di-O-benzoyl-2,6-dideoxy-α-D-ribohexopyranoside 
• 64429-65-8 methyl 3,4-di-O-benzoyl-2,6-dideoxy-β-L-lyxo-hexopyranoside 
• 32476-34-9 Methyl 3,4-di-O-benzoyl-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 939050-83-6 C₆H₁₀O₃C₆H₆S 
• 939050-45-0 C₆H₁₀O₃C₆H₆S 
• 2873-29-2 D-glucal triacetate 
• 76739-66-7 3,4-di-O-acetyl-D-rhamnal 
• 98-88-4 benzoyl chloride 
• 363134-99-0 diacetyl-d-glucal-6-bromohydrin 
• 18546-25-3 6-O-p-tolylsulfonyl-3,4-di-O-acetyl-D-glucal 

Downstream Products

• 106988-68-5 C₂₀H₁₉ClO₅ 
• 128461-95-0 C₃₀H₂₆O₆ 
• 130780-27-7 C₃₀H₂₆O₆ 
• 130780-28-8 C₃₀H₂₆O₆ 
• 128461-95-0 C₃₀H₂₆O₆ 
• 106988-75-4 1,5-Anhydro-2,6-didesoxy-3-O-(4-methoxybenzyl)-L-ribo-hex-1-enit 
• 106988-76-5 1,5-Anhydro-2,6-didesoxy-4-O-(4-methoxybenzyl)-L-ribo-hex-1-enit 
• 106988-77-6 1,5-Anhydro-4-O-benzoyl-2,6-didesoxy-3-O-(4-methoxybenzyl)-L-ribo-hex-1-enit 
• 107079-29-8 1,5-Anhydro-3,4-di-O-benzoyl-2,6-didesoxy-L-ribo-hex-1-enit 
• 106988-68-5 3,4-Di-O-benzoyl-2,6-didesoxy-α-L-ribo-hexopyranosylchlorid 
• 128461-96-1 C₃₀H₂₆O₆ 
• 128462-02-2 C₃₇H₃₄O₉ 
• 128462-00-0 C₃₁H₂₈O₇ 
• 128461-97-2 C₃₀H₂₆O₆ 

Relevant academic research and scientific papers

Direct and stereoselective synthesis of β-linked 2,6- deoxyoligosaccharides

(Chemical Equation Presented) Short and sweet: Glycosidation of 2-deoxyglycosyl imidates with I2 as shown in the scheme (Bn = benzyl, Bz = benzoyl, MS = molecular sieves) proceeds smoothly to provide the corresponding β-linked 2-deoxyglycosides

Improvement in O -> C Glycoside Rearrangement Approach to C-Aryl Glycosides: Use of 1-O-Acetyl Sugar as Stable but Efficient Glycosyl Donor

1-O-Acetyl sugars serve as efficient glycosyl donor in the O -> C-glycoside rearrangement approach to C-aryl glycosides.Model study was carried out on three types of 2-deoxy-glycosyl acetates including amino sugar derivative.Comparison of the promoters, Cp2HfCl2-AgClO4, SnCl4, BF3*OEt2 is described.

Synthetic Study toward Vineomycins. Synthesis of C-Aryl Glycoside Sector via Cp2HfCl2-AgClO4-Promoted Tactics

Regio- and stereo-controlled formation of C-aryl β-D-olivoside linkage is achieved by the reaction of naphthol or anthrol derivatives with D-olivosyl fluoride.The reaction is efficiently promoted by Cp2HfCl2-AgClO4 and the bond formation occurs selectivit