allyl 2,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside

Base Information

• Chemical Name: allyl 2,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside
• CAS No.: 1315192-47-2
• Molecular Formula: C₄₃H₅₀O₉
• Molecular Weight: 710.865

Synonyms:allyl 2,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside

Chemical Property of allyl 2,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside

Chemical Property:

Purity/Quality:

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Technology Process of allyl 2,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside

There total 1 articles about allyl 2,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside 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:

C45H52O10 → allyl 2,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside (1315192-47-2)

Guidance literature:

With sodium methylate; In methanol; acetonitrile; for 4h;

DOI:10.1016/j.tetlet.2011.05.089

Reference yield: 59.0%

C37H45N3O8 + allyl 2,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside (1315192-47-2) → C77H89N3O16 (1315192-55-2)

Guidance literature:

With N-iodo-succinimide; trifluorormethanesulfonic acid; In acetonitrile; at 20 ℃; for 0.333333h; stereoselective reaction; Inert atmosphere;

DOI:10.1016/j.tetlet.2011.05.089

Reference yield:

C25H30O6 + allyl 2,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside (1315192-47-2) → C65H74O14

Guidance literature:

With N-iodo-succinimide; trifluorormethanesulfonic acid; In acetonitrile; at 20 ℃; for 0.2h; stereoselective reaction; Inert atmosphere;

DOI:10.1016/j.tetlet.2011.05.089

Downstream raw materials:

C₇₇H₈₉N₃O₁₆

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