3-O-[4-O-benzyl-2,3,6-trideoxy-α-L-threo-hex-2-enopyranosyl]-1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol

Base Information

• Chemical Name: 3-O-[4-O-benzyl-2,3,6-trideoxy-α-L-threo-hex-2-enopyranosyl]-1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol
• CAS No.: 1615710-97-8
• Molecular Formula: C₂₆H₃₀O₅
• Molecular Weight: 422.521
• Mol file: 1615710-97-8.mol

Synonyms:3-O-[4-O-benzyl-2,3,6-trideoxy-α-L-threo-hex-2-enopyranosyl]-1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol

Chemical Property of 3-O-[4-O-benzyl-2,3,6-trideoxy-α-L-threo-hex-2-enopyranosyl]-1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-O-[4-O-benzyl-2,3,6-trideoxy-α-L-threo-hex-2-enopyranosyl]-1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol

There total 1 articles about 3-O-[4-O-benzyl-2,3,6-trideoxy-α-L-threo-hex-2-enopyranosyl]-1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 40.0%

1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol (137035-65-5) → 3-O-[4-O-benzyl-2,3,6-trideoxy-α-L-threo-hex-2-enopyranosyl]-1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol (1615710-97-8) + 3-O-[4-O-benzyl-2,3,6-trideoxy-β-L-threo-hex-2-enopyranosyl]-1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol (1615710-98-9)

Guidance literature:

1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol; With sodium hydroxide; In water; toluene; for 0.333333h;

With tetra-(n-butyl)ammonium iodide; p-toluenesulfonyl chloride; In water; toluene; at 20 ℃;

DOI:10.1016/j.tetlet.2014.05.025

Reference yield: 10.0%

3-O-[4-O-benzyl-2,3,6-trideoxy-α-L-threo-hex-2-enopyranosyl]-1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol (1615710-97-8) + 2',3'-bis-O-(tert-butyldimethylsilyl)uridine (87418-87-9,69504-12-7) → C47H70N2O11Si2 + C47H70N2O11Si2 + C34H54N2O8Si2 + C34H54N2O8Si2 + C34H56N2O9Si2

Guidance literature:

With triphenylphosphine hydrobromide; In dichloromethane; at 0 ℃; Temperature; Molecular sieve;

Reference yield:

3-azidopropan-1-ol (72320-38-8) + 3-O-[4-O-benzyl-2,3,6-trideoxy-α-L-threo-hex-2-enopyranosyl]-1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol (1615710-97-8) → (3-azidopropyl) 3-O-[4-O-benzyl-2,3,6-trideoxy-α-L-threo-hex-2-enopyranosyl]-4-O-benzyl-2,6-dideoxy-L-lyxo-hexopyranoside + (3-azidopropyl) 3-O-[4-O-benzyl-2,3,6-trideoxy-α-L-threo-hex-2-enopyranosyl]-4-O-benzyl-2,6-dideoxy-L-lyxo-hexopyranoside

Guidance literature:

With triphenylphosphine hydrobromide; In dichloromethane; at -10 - 20 ℃; Overall yield = 40 %; Overall yield = 49 mg; Molecular sieve;

upstream raw materials:

1,5-anhydro-4-O-benzyl-2,6-dideoxy-L-lyxo-hex-1-enitol