1-O-(5-O-(5-O-acetyl-2,3-di-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl) trichloroacetimidate

Base Information

Chemical Name:1-O-(5-O-(5-O-acetyl-2,3-di-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl) trichloroacetimidate
CAS No.:1352996-32-7
Molecular Formula:C₄₂H₃₆Cl₃NO₁₄
Molecular Weight:885.105
Hs Code.:

Synonyms:1-O-(5-O-(5-O-acetyl-2,3-di-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl) trichloroacetimidate

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Chemical Property of 1-O-(5-O-(5-O-acetyl-2,3-di-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl) trichloroacetimidate

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Technology Process of 1-O-(5-O-(5-O-acetyl-2,3-di-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl) trichloroacetimidate

There total 1 articles about 1-O-(5-O-(5-O-acetyl-2,3-di-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl) trichloroacetimidate 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: 94.0%

: 5-O-acetyl-2,3-di-O-benzoyl-α-D-arabinofuranosyl-(1->5)-2,3-di-O-benzoyl-D-arabinofuranose

: 545-06-2
trichloroacetonitrile

: 1352996-32-7
1-O-(5-O-(5-O-acetyl-2,3-di-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl) trichloroacetimidate

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 0 ℃; for 0.166667h;
DOI:10.1093/glycob/cwr068

Reference yield: 88.0%

: 1352996-26-9
8-O-hexadecyl-3,6,10-trioxa-1,8-hexacosanediol

: 1352996-32-7
1-O-(5-O-(5-O-acetyl-2,3-di-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl) trichloroacetimidate

: 1352996-38-3
C₇₉H₁₁₄O₁₈

Guidance literature:: With boron trifluoride diethyl etherate; In dichloromethane; at 20 ℃; for 0.5h; Molecular sieve; Inert atmosphere;
DOI:10.1093/glycob/cwr068

Reference yield: 88.0%

: 1352996-32-7
1-O-(5-O-(5-O-acetyl-2,3-di-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl) trichloroacetimidate

: 1352996-44-1
p-tolyl-2,3-di-O-benzoyl-α-D-arabinofuranosyl-(1->5)-[2,3-di-O-benzoyl-α-D-arabinofuranosyl-(1->2)]-3-O-benzoyl-1-thio-α-D-arabinofuranoside

: p-tolyl-5-O-acetyl-2,3-di-O-benzoyl-α-D-arabinofuranosyl-(1->5)-2,3-di-O-benzoyl-α-D-arabinofuranosyl-(1->5)-2,3-di-O-benzoyl-α-D-arabinofuranosyl-(1->5)-[5-O-acetyl-2,3-di-O-benzoyl-α-D-arabinofuranosyl-(1->5)-2,3-di-O-benzoyl-α-D-arabinofuranosyl-(1->5)-2,3-di-O-benzoyl-α-D-arabinofuranosyl-(1->2)]-3-O-benzoyl-1-thio-α-D-arabinofuranoside

Guidance literature:: With boron trifluoride diethyl etherate; In dichloromethane; at 20 ℃; for 0.5h; Molecular sieve; Inert atmosphere;
DOI:10.1093/glycob/cwr068