199116-18-2

Upstream product

• 13265-84-4 D-glucal 
• 187880-20-2 2,6-anhydro-5-deoxy-1,3-O-(4-methoxybenzylidene)-D-arabino-hex-5-enitol 
• 2186-92-7 p-Anisaldehyde dimethyl acetal 
• 13154-24-0 triisopropylsilyl chloride 
• 187879-14-7 4,6-O-(4-methoxybenzylidene)-3-O-(triisopropyl)silyl-D-(-)-glucal 

Downstream Products

• 629652-46-6 4,6-di-O-(4-methoxybenzyl)-2-deoxy-α,β-D-glucopyranose 
• 629652-48-8 2-deoxy-4,6-di-O-(4-methoxybenzyl)-D-gluco-γ-lactone 
• 629652-49-9 2-deoxy-1,3-dioxo-4,6-di-O-(4-methoxybenzyl)-D-(+)-glucopyranose 
• 629652-43-3 4,6-di-O-(4-methoxybenzyl)-2-deoxy-3-O-(triisopropyl)silyl-α,β-D-glucopyranose 
• 629652-50-2 (2R,3R,4S,4aR,7R,8R,9aR)-3,4-Bis-benzyloxy-2-benzyloxymethyl-8-(4-methoxy-benzyloxy)-7-(4-methoxy-benzyloxymethyl)-2,3,4a,7,8,9a-hexahydro-4H-1,6,9-trioxa-10-thia-anthracen-5-one 
• 199116-19-3 C₈₀H₁₀₂O₁₅Si₂ 
• 196704-96-8 4-O-p-methoxybenzyl-D-glucal 
• 629652-41-1 4,6-di-O-(4-methoxybenzyl)-3-O-(triisopropyl)silyl-D-(-)-glucal 

Relevant academic research and scientific papers

Totally Stereoselective Synthesis of 1,3-Disaccharides through Diels-Alder Reactions

A nonclassical, totally stereoselective synthesis of orthogonally protected 1,3-disaccharides is reported. Enantiomerically pure β-keto-δ-lactones, efficiently obtained from glucal and galactal, are transformed into electron-poor heterodienes and chemo-,

A highly convergent total synthetic route to glycopeptides carrying a high-mannose core pentasaccharide domain N-linked to a natural peptide motif

N-Linked glycopeptides were synthesized by condensation of a high-mannose anomeric amine bearing a pentasaccharide with aspartic-acid-containing tri- and pentapeptides through the agency of IIDQ. The pentasaccharide portion, corresponding to the 'core' re