161835-17-2

Basic information

• Product Name: 1,2-anhydro-3,5-di-O-benzyl-β-D-lyxofuranose
• Synonyms: 1,2-anhydro-3,5-di-O-benzyl-β-D-lyxofuranose
• CAS NO: 161835-17-2
• Molecular Weight: 312.365
• Mol File: 161835-17-2.mol

Chemical Properties

• CAS DataBase Reference: 1,2-anhydro-3,5-di-O-benzyl-β-D-lyxofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-anhydro-3,5-di-O-benzyl-β-D-lyxofuranose(161835-17-2)
• EPA Substance Registry System: 1,2-anhydro-3,5-di-O-benzyl-β-D-lyxofuranose(161835-17-2)

Safety Data

• Hazardous Substances Data: 161835-17-2(Hazardous Substances Data)

Upstream product

• 16054-77-6 3,5-di-O-benzyl-D-xylofuranose 
• 41341-99-5 3,5-di-O-benzyl-1,2-O-isopropylidene-α-D-xylofuranose 

Downstream Products

• 161835-18-3 O-(3,5-Di-O-benzyl-α-D-lyxofuranosyl)-(1->6)-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 1314093-27-0 (2S,3R,4R,5R)-2-azido-4-benzyloxy-5-(benzyloxymethyl)tetrahydrofuran-3-ol 
• 1314093-38-3 (5aS,6S,7R,8aS)-6-benzyloxy-7-(benzyloxymethyl)-5a,6,7,8a-tetrahydro-4H-furo[3,2-b][1,2,3]triazolo[1,5-d][1,4]oxazine 
• 1314093-66-7 ethyl 2-((2S,3S,4S,5R)-2-azido-4-benzyloxy-5-benzyloxymethyl-tetrahydrofuran-3-yloxy)acetate 
• 161835-21-8 1,2-anhydro-3,5-di-O-benzyl-α-D-xylofuranose 
• 79083-39-9 1-O-methyl 3,5-di-O-benzyl β(D)xylo-pentoaldofuranose 
• 159148-13-7 Methyl 3,5-di-O-benzyl-α-D-lyxofuranoside 

Relevant articles and documents

A facile synthesis of 1,2-anhydroglycofuranose benzyl ethers

The synthesis of 1,2-anhydromanno-, -lyxo-, -gluco-, and -xylofuranose benzyl ethers was successfully achieved via intramolecular S(N)2 reaction of the corresponding C-1 alkoxide with C-2 bearing tosyloxy group. The key intermediates, furanose 2-sulfonate

Synthesis and glycosidic reaction of 1,2-anhydromanno-, lyxo-, gluco-, and xylofuranose perbenzyl ethers

Stereospecific synthesis of 1,2-anhydromanno-, lyxo-, gluco-, and xylofuranose perbenzyl ethers was successfully achieved via intramolecular SN2 reaction of the corresponding C-1 alkoxide with C-2 bearing tosyloxy group. The key intermediates, furanose 2-sulfonates, were prepared from the corresponding 1,2-diols and tosyl chloride under phase transfer conditions in good yields. Condensation of the anhydro sugars with 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose or N-benzyloxycarbonyl L-serine methyl ester in the absence of catalyst gave 1,2-trans-linked glycofuranosides in high yield.