1,6-anhydro-4-O-benzyl-3-O-(2-naphthalenylmethyl)-2-O-[N-[benzyl(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)uronate]ethanimidyl]-β-D-mannopyranose

Base Information

• Chemical Name: 1,6-anhydro-4-O-benzyl-3-O-(2-naphthalenylmethyl)-2-O-[N-[benzyl(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)uronate]ethanimidyl]-β-D-mannopyranose
• CAS No.: 1607445-05-5
• Molecular Formula: C₆₀H₅₉NO₁₁
• Molecular Weight: 970.129
• Mol file: 1607445-05-5.mol

Synonyms:1,6-anhydro-4-O-benzyl-3-O-(2-naphthalenylmethyl)-2-O-[N-[benzyl(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)uronate]ethanimidyl]-β-D-mannopyranose

Chemical Property of 1,6-anhydro-4-O-benzyl-3-O-(2-naphthalenylmethyl)-2-O-[N-[benzyl(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)uronate]ethanimidyl]-β-D-mannopyranose

Chemical Property:

Purity/Quality:

Safty Information:

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Useful:

Technology Process of 1,6-anhydro-4-O-benzyl-3-O-(2-naphthalenylmethyl)-2-O-[N-[benzyl(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)uronate]ethanimidyl]-β-D-mannopyranose

There total 1 articles about 1,6-anhydro-4-O-benzyl-3-O-(2-naphthalenylmethyl)-2-O-[N-[benzyl(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)uronate]ethanimidyl]-β-D-mannopyranose 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:

benzyl 2,3,4-tri-O-benzyl-1-O-(trichloroacetimidoyl)-α-D-glucopyranuronate (184698-69-9,159420-94-7) + 1,6-anhydro-4-O-benzyl-3-O-(2-naphthalenylmethyl)-β-D-mannopyranose → 1,6-anhydro-4-O-benzyl-3-O-(2-naphthalenylmethyl)-2-O-[N-[benzyl(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)uronate]ethanimidyl]-β-D-mannopyranose (1607445-05-5) + 1,6-anhydro-4-O-benzyl-3-O-(2-naphthalenylmethyl)-2-O-[N-[benzyl(2,3,4-tri-O-benzyl-β-D-glucopyranosyl)uronate]ethanimidyl]-β-D-mannopyranose

Guidance literature:

With boron trifluoride diethyl etherate; In dichloromethane; acetonitrile; at -78 ℃; for 1.5h; Overall yield = 52 %; Overall yield = 131 mg; stereoselective reaction; Molecular sieve; Inert atmosphere;

DOI:10.1016/j.carres.2014.01.022

upstream raw materials:

benzyl 2,3,4-tri-O-benzyl-1-O-(trichloroacetimidoyl)-α-D-glucopyranuronate