629652-49-9

Upstream product

• 629652-43-3 4,6-di-O-(4-methoxybenzyl)-2-deoxy-3-O-(triisopropyl)silyl-α,β-D-glucopyranose 
• 629652-41-1 4,6-di-O-(4-methoxybenzyl)-3-O-(triisopropyl)silyl-D-(-)-glucal 
• 629652-46-6 4,6-di-O-(4-methoxybenzyl)-2-deoxy-α,β-D-glucopyranose 
• 13265-84-4 D-glucal 
• 187879-14-7 4,6-O-(4-methoxybenzylidene)-3-O-(triisopropyl)silyl-D-(-)-glucal 
• 199116-18-2 4-O-(4-methoxybenzyl)-3-O-(triisopropyl)silyl-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 
• 629652-48-8 2-deoxy-4,6-di-O-(4-methoxybenzyl)-D-gluco-γ-lactone 

Downstream Products

• 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 

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-,