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GlycoDepot

4-Methylphenyl 2-O-benzoyl-4,6-di-O-benzyl-3-O-(9-fluorenylmethoxycarbonyl)-1-thio-β-D-glucopyranoside

4-Methylphenyl 2-O-benzoyl-4,6-di-O-benzyl-3-O-(9-fluorenylmethoxycarbonyl)-1-thio-β-D-glucopyranoside 4-Methylphenyl 2-O-benzoyl-4,6-di-O-benzyl-3-O-(9-fluoren…

4-Methylphenyl 2-O-benzoyl-4,6-di-O-benzyl-3-O-(9-fluorenylmethoxycarbonyl)-1-thio-β-D-glucopyranoside
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  • ISO 9001:2015 facilities · CoA + batch tracking with every shipment
  • Worldwide shipping · dry-ice option for thermolabile reagents
  • Research Use Only — not for human or veterinary clinical use

About this product

4-Methylphenyl 2-O-benzoyl-4,6-di-O-benzyl-3-O-(9-fluorenylmethoxycarbonyl)-1-thio-β-D-glucopyranoside 4-Methylphenyl 2-O-benzoyl-4,6-di-O-benzyl-3-O-(9-fluorenylmethoxycarbonyl)-1-thio-β-D-glucopyranoside is a thioglycoside building block engineered for controlled oligosaccharide synthesis, featuring a strategic combination of orthogonal protecting groups to enable selective deprotection during carbohydrate assembly. Core Structure Backbone : β-D-glucopyranose ring with a 4-methylphenylthio group at the anomeric position (C1), serving as a glycosyl donor activated by thiophilic promoters (e.g., NIS/TfOH). Orthogonal Protecting Groups Position Group Stability & Deprotection C2 Benzoyl ester Base-labile (removed via NaOH/MeOH) C3 Fmoc (9-fluorenylmethoxycarbonyl) Base-sensitive (cleaved with 20% piperidine/DMF) C4/C6 Benzyl ethers Acid-stable; removed via hydrogenolysis (H₂/Pd-C) Key Properties Molecular formula : C₄₉H₄₅NO₈S (estimated) Molecular weight : ~832.0 g/mol Reactivity : Benzoyl at C2 moderates donor reactivity via electron withdrawal. Fmoc at C3 enables compatibility with solid-phase synthesis workflows. Synthetic Utility Sequential Deprotection : Step 1 : Fmoc removal (C3) under mild basic conditions. Step 2 : Benzoyl cleavage (C2) via alkaline hydrolysis. Step 3 : Benzyl deprotection (C4/C6) via hydrogenolysis. Glycosylation Control : The 4-methylphenylthio group ensures efficient activation for glycosidic bond formation. Benzyl groups at C4/C6 provide steric shielding to direct regioselective coupling. Branching Flexibility : Exposed C3-OH after Fmoc removal allows site-specific modifications (e.g., phosphorylation, conjugation). Applications Glycoconjugate vaccines : Selective C3 functionalization for antigen attachment. Dendrimer synthesis : Iterative branching via orthogonal deprotection. Glycosidase inhibitor design : Protected glucose scaffold for analog development. Stability Profile Condition Stability Acidic (pH > 3) Stable (benzyl/benzoyl intact) Basic (pH < 9) Stable except during Fmoc/benzoyl cleavage Hydrogenation Tolerated until final benzyl removal This compound exemplifies advanced carbohydrate engineering, integrating traditional protecting groups (benzyl, benzoyl) with modern orthogonal motifs (Fmoc) for precision synthesis of complex glycans. Its design supports both solution-phase and automated solid-phase methodologies. Citations: https://patents.google.com/patent/WO2000042057A1/en https://www.frontiersin.org/journals/chemistry/articles/10.3389/fchem.2023.1332837/full https://pubmed.ncbi.nlm.nih.gov/31895493/ https://europepmc.org/article/pmc/6531329 https://pubs.rsc.org/en/content/getauthorversionpdf/c9ob00573k https://pmc.ncbi.nlm.nih.gov/articles/PMC6259426/ https://pmc.ncbi.nlm.nih.gov/articles/PMC2952681/ https://onlinelibrary.wiley.com/doi/full/10.1002/asia.201901621

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