83562-59-8

Basic information

• Product Name: 1-O-acetyl-2,3,4-tri-O-benzyl-α-L-fucopyranose
• Synonyms: 1-O-acetyl-2,3,4-tri-O-benzyl-α-L-fucopyranose
• CAS NO: 83562-59-8
• Molecular Weight: 476.569
• Mol File: 83562-59-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-O-acetyl-2,3,4-tri-O-benzyl-α-L-fucopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-acetyl-2,3,4-tri-O-benzyl-α-L-fucopyranose(83562-59-8)
• EPA Substance Registry System: 1-O-acetyl-2,3,4-tri-O-benzyl-α-L-fucopyranose(83562-59-8)

Safety Data

• Hazardous Substances Data: 83562-59-8(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 74841-88-6 methyl 2,3,4-tri-O-benzyl-β-L-fucopyranoside 
• 33639-74-6 (2R,3S,4R,5R,6S)-3,4,5-tris(benzyloxy)-2-methoxy-6-methyltetrahydro-2H-pyran 
• 162118-38-9 (3S,4R,5R,6S)-3,4,5-tris(benzyloxy)-6-methyltetrahydro-2H-pyran-2-ol 

Downstream Products

• 679430-83-2 1-acetamido-2,3,4-tri-O-benzyl-α-L-fucopyranose 
• 679430-81-0 1-azido-2,3,4-tri-O-benzyl-α-L-fucopyranose 
• 250691-61-3 (2S,3S,4R,5R,6S)-3,4,5-Tris-benzyloxy-2-iodo-6-methyl-tetrahydro-pyran 
• 33639-77-9 perbenzyl fucosyl bromide 
• 163059-64-1 1-bromo-2,3,4-tri-O-benzylfucopyranoside 

Relevant articles and documents

Sweet (hetero)aromatics: Glycosylated templates for the construction of saccharide mimetics

Mono- and diglycosylated aromatics and heteroaromatics may serve as building blocks for the construction of metabolically stable mimetics of oligosaccharides. Methods for their preparation from monosaccharidic precursors by direct C-glycosylation, dipolar cycloaddition or Larock cyclization are described.

2'-Deoxy-2'-alkoxyaminouridines: Novel 2'-substituted uridines prepared by intramolecular nucleophilic ring opening of 2,2'-O-anhydrouridines

Natural and unnatural modified nucleosides and nucleotides play important roles in biology, medicine, and as biomedical research tools. Reported herein is an application of synthetic methodology developed for the stereo- and regiospecific introduction of structural modifications at the 2'-position of uridine nucleosides. A novel class of modified nucleosides, 2'-alkoxylamino-2'-deoxy uridines, are prepared by intramolecular nucleophilic addition of a 3'-tethered alkoxycarbamate nucleophile to the 2'-position with concomitant opening of a 2,2'-anhydrouridine.