383406-90-4

Upstream product

• 128848-50-0 phenyl 2,3,4,6-tetra-O-trimethylsilyl-1-thio-β-D-glucopyranoside 
• 128848-51-1 phenyl 3-O-benzyl-4,6-O-benzylidene-1-deoxy-1-thio-β-D-glucopyranoside 
• 2936-70-1 (2R,3S,4S,5R,6S)-2-Hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3,4,5-triol 
• 100-51-6 benzyl alcohol 
• 383406-89-1 benzyl 2,4-di-O-acetyl-3,6-di-O-benzyl-β-D-glucopyranoside 

Downstream Products

• 383406-92-6 benzyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)-[(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->4)]-3,6-di-O-benzyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

Iron(iii) chloride-tandem catalysis for a one-pot regioselective protection of glycopyranosides

Tandem catalysis by using iron(iii) chloride hexahydrate leads to carbohydrate building blocks displaying an orthogonal protecting group pattern as illustrated by the regioselective protection of trehalose and maltose disaccharides.

Synthesis of peracetylated chacotriose

Steroidal glycoalkaloids of many Solanum species have recognized biological activities, especially those containing the glycosyl moiety α-L-rhamnopyranosyl-(1 → 2)-[α-L-rhamnopyranosyl-(1 → 4)]-D-glucopyranose (chacotriose) whose peracetate is here synthe