286476-61-7

Upstream product

• 98-88-4 benzoyl chloride 
• 41308-77-4 allyl α-L-fucopyranoside 
• 108182-34-9 allyl 3,4-di-O-isopropylidene-α-L-fucopyranoside 
• 286476-60-6 allyl 2-O-benzoyl-3,4-O-isopropylidene-α-L-fucopyranoside 

Downstream Products

• 286476-64-0 allyl (4,6-di-O-acetyl-3-O-allyloxycarbonyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-2,4-di-O-benzoyl-α-L-fucopyranoside 
• 286476-63-9 allyl (3-O-allyloxycarbonyl-2-deoxy-4,6-isopropylidene-2-phthalimido-β-D-glucopyranosyl)-(1->3)-2,4-di-O-benzoyl-α-L-fucopyranoside 
• 286476-65-1 allyl (4,6-di-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-2,4-di-O-benzoyl-α-L-fucopyranoside 
• 286476-62-8 allyl 2,4-di-O-benzoyl-α-L-fucopyranoside 

Relevant academic research and scientific papers

2,4-Diazido-2,4,6-trideoxy-L-hexopyranoses as valuable building units in the synthesis of natural products

Synthesis of five L-enantiomers of 2,4-diazido-2,4,6-trideoxy-pyranoses has been accomplished. These sugars were prepared via the regioselective protection of hydroxyl groups in L-rhamnoside and L-fucoside, followed by triflation and subsequent SN/s

Synthesis and conjugation of a sulfated disaccharide involved in the aggregation process of the marine sponge Microciona prolifera

The synthesis is reported of allyl (sodium 2-acetamido-2-deoxy-β-D-glucopyranosyl 3-sulfate)-(1→3)-α-L-fucopyranoside which represents an oligosaccharide fragment of the aggregation factor of the marine sponge Microciona prolifera. The title compound was