475652-79-0

Upstream product

• 130323-36-3 3,6-di-O-benzoyl-D-galactal 
• 124-63-0 methanesulfonyl chloride 
• 98-88-4 benzoyl chloride 
• 21193-75-9 D-galactal 

Downstream Products

• 475630-55-8 C₂₀H₁₉NO₆ 
• 475630-51-4 4-azido-4-deoxy-3,6-di-O-benzoyl-D-galactal 

Relevant academic research and scientific papers

Synthesis of γ-aminobutyric acid analogs based on carbohydrate scaffolds

γ-Aminobutyric acid analogs based on sugar scaffolds were prepared in six to nine steps starting from d-glucal and d-galactal. The key step in the synthesis is the Vilsmeier-Haack reaction that affords the corresponding 2-C-formyl glycal on treatment with

Glycal-mediated syntheses of enantiomerically pure polyhydroxylated γ- and δ-lactams

Syntheses of new enantiomerically pure γ-lactams 4a,b and δ-lactams 5a,b from D-glucal (3a) and D-galactal (3b) as starting materials are described.