E-ethyl <(1-N-5,6-di-O-benzoyl-2-deoxy-1,3-di-N-p-tolylsulfonylstreptamin-4-yl) 3,4-di-O-benzoyl-2,6,7-trideoxy-2-p-tolylsulfonamido-α-D-gluco-oct-6-enopyranosid>uronate

Base Information

• Chemical Name: E-ethyl <(1-N-5,6-di-O-benzoyl-2-deoxy-1,3-di-N-p-tolylsulfonylstreptamin-4-yl) 3,4-di-O-benzoyl-2,6,7-trideoxy-2-p-tolylsulfonamido-α-D-gluco-oct-6-enopyranosid>uronate
• CAS No.: 88897-28-3
• Molecular Formula: C₇₂H₆₇N₃O₁₉S₃
• Molecular Weight: 1374.53
• Mol file: 88897-28-3.mol

Synonyms:

Chemical Property of E-ethyl <(1-N-5,6-di-O-benzoyl-2-deoxy-1,3-di-N-p-tolylsulfonylstreptamin-4-yl) 3,4-di-O-benzoyl-2,6,7-trideoxy-2-p-tolylsulfonamido-α-D-gluco-oct-6-enopyranosid>uronate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of E-ethyl <(1-N-5,6-di-O-benzoyl-2-deoxy-1,3-di-N-p-tolylsulfonylstreptamin-4-yl) 3,4-di-O-benzoyl-2,6,7-trideoxy-2-p-tolylsulfonamido-α-D-gluco-oct-6-enopyranosid>uronate

There total 1 articles about E-ethyl <(1-N-5,6-di-O-benzoyl-2-deoxy-1,3-di-N-p-tolylsulfonylstreptamin-4-yl) 3,4-di-O-benzoyl-2,6,7-trideoxy-2-p-tolylsulfonamido-α-D-gluco-oct-6-enopyranosid>uronate 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:

(1-N-5,6-di-O-benzoyl-2-deoxy-1,3-di-N-p-tolylsulfonylstreptamin-4-yl) 3,4-di-O-benzoyl-2-deoxy-2-p-tolylsulfonamido-α-D-gluco-hexodialdo-1,5-pyranoside (88897-27-2) + ethyl (triphenylphosphoranylidene)acetate (1099-45-2) → E-ethyl <(1-N-5,6-di-O-benzoyl-2-deoxy-1,3-di-N-p-tolylsulfonylstreptamin-4-yl) 3,4-di-O-benzoyl-2,6,7-trideoxy-2-p-tolylsulfonamido-α-D-gluco-oct-6-enopyranosid>uronate (88897-28-3)

Guidance literature:

In benzene; Yield given; Ambient temperature;

DOI:10.1016/0008-6215(84)85280-5

Reference yield: 66.0%

E-ethyl <(1-N-5,6-di-O-benzoyl-2-deoxy-1,3-di-N-p-tolylsulfonylstreptamin-4-yl) 3,4-di-O-benzoyl-2,6,7-trideoxy-2-p-tolylsulfonamido-α-D-gluco-oct-6-enopyranosid>uronate (88897-28-3) → ethyl <(1-N-5,6-di-O-benzoyl-2-deoxy-1,3-di-N-p-tolylsulfonylstreptamin-4-yl) 3,4-di-O-benzoyl-2-deoxy-2-p-tolylsulfonamido-L-threo-α-D-gluco-octo-1,5-pyranosid>uronate (88897-29-4,88929-73-1) + ethyl <(1-N-5,6-di-O-benzoyl-2-deoxy-1,3-di-N-p-tolylsulfonylstreptamin-4-yl) 3,4-di-O-benzoyl-2-deoxy-2-p-tolylsulfonamido-D-threo-α-D-gluco-octo-1,5-pyranosid>uronate (88897-29-4,88929-73-1)

Guidance literature:

With pyridine; osmium(VIII) oxide; Ambient temperature;

DOI:10.1016/0008-6215(84)85280-5

upstream raw materials:

(1-N-5,6-di-O-benzoyl-2-deoxy-1,3-di-N-p-tolylsulfonylstreptamin-4-yl) 3,4-di-O-benzoyl-2-deoxy-2-p-tolylsulfonamido-α-D-gluco-hexodialdo-1,5-pyranoside

ethyl (triphenylphosphoranylidene)acetate

Downstream raw materials:

ethyl <(1-N-5,6-di-O-benzoyl-2-deoxy-1,3-di-N-p-tolylsulfonylstreptamin-4-yl) 3,4-di-O-benzoyl-2-deoxy-2-p-tolylsulfonamido-L-threo-α-D-gluco-octo-1,5-pyranosid>uronate

ethyl <(1-N-5,6-di-O-benzoyl-2-deoxy-1,3-di-N-p-tolylsulfonylstreptamin-4-yl) 3,4-di-O-benzoyl-2-deoxy-2-p-tolylsulfonamido-D-threo-α-D-gluco-octo-1,5-pyranosid>uronate