635684-82-1

Upstream product

• 100-39-0 benzyl bromide 
• 635684-81-0 2,2,2-Trichloro-N-((4aR,6S,7R,8R,8aS)-6-ethylsulfanyl-8-hydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-acetamide 
• 635684-80-9 ethyl 2-deoxy-2-N-trichloroacetamido-1-thio-β-D-glucopyranoside 
• 5573-62-6 (ethylthio)trimethylsilane 
• 100-52-7 benzaldehyde 
• 169557-88-4 ethyl-3,4,6-tri-O-acetyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamido)-1-thio-β-D-glucopyranoside 

Downstream Products

• 399035-91-7 ethyl 4-O-acetyl-3,6-di-O-benzyl-2-deoxy-1-thio-2-trichloroacetamido-β-D-glucopyranoside 

Relevant academic research and scientific papers

Stereocontrolled synthesis of fully functionalized D-glucosamine monosaccharides via a domino nitro-Michael/Henry reaction

A diastereoselective domino nitro-Michael/Henry reaction involving a β-hydroxyaldehyde and a nitroalkene provides direct access to fully functionalized D-glucosamine monosaccharides. The Royal Society of Chemistry.

Efficient synthesis of two HNK-1 related pentasaccharides

Two pentasaccharides, representative of those found on complex N-glycans, were synthesized for use as potential substrates for sulfotransferases. The synthesis was achieved by the addition of a disaccharide donor β-D-GlcA(1→3)α-D-Gal-trichloroacetimidate