O-4-O-(tert-butyldimethyl)silyl-α-rhodinosyl-(1->3)-O-6-O-acetyl-4-O-benzoyl-2-deoxy-2-iodo-β-glucopyranosyl-(1->4)-6-O-acetyl-3-O-benzoyl-2-deoxy-2-iodo-1-O-trichloroacetimidyl-α-D-glucopyranose

Base Information

Chemical Name:O-4-O-(tert-butyldimethyl)silyl-α-rhodinosyl-(1->3)-O-6-O-acetyl-4-O-benzoyl-2-deoxy-2-iodo-β-glucopyranosyl-(1->4)-6-O-acetyl-3-O-benzoyl-2-deoxy-2-iodo-1-O-trichloroacetimidyl-α-D-glucopyranose
CAS No.:288859-50-7
Molecular Formula:C₄₄H₅₆Cl₃I₂NO₁₅Si
Molecular Weight:1227.18
Hs Code.:

O-4-O-(tert-butyldimethyl)silyl-α-rhodinosyl-(1->3)-O-6-O-acetyl-4-O-benzoyl-2-deoxy-2-iodo-β-glucopyranosyl-(1->4)-6-O-acetyl-3-O-benzoyl-2-deoxy-2-iodo-1-O-trichloroacetimidyl-α-D-glucopyranose

Synonyms:O-4-O-(tert-butyldimethyl)silyl-α-rhodinosyl-(1->3)-O-6-O-acetyl-4-O-benzoyl-2-deoxy-2-iodo-β-glucopyranosyl-(1->4)-6-O-acetyl-3-O-benzoyl-2-deoxy-2-iodo-1-O-trichloroacetimidyl-α-D-glucopyranose

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Chemical Property of O-4-O-(tert-butyldimethyl)silyl-α-rhodinosyl-(1->3)-O-6-O-acetyl-4-O-benzoyl-2-deoxy-2-iodo-β-glucopyranosyl-(1->4)-6-O-acetyl-3-O-benzoyl-2-deoxy-2-iodo-1-O-trichloroacetimidyl-α-D-glucopyranose

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Technology Process of O-4-O-(tert-butyldimethyl)silyl-α-rhodinosyl-(1->3)-O-6-O-acetyl-4-O-benzoyl-2-deoxy-2-iodo-β-glucopyranosyl-(1->4)-6-O-acetyl-3-O-benzoyl-2-deoxy-2-iodo-1-O-trichloroacetimidyl-α-D-glucopyranose

There total 2 articles about O-4-O-(tert-butyldimethyl)silyl-α-rhodinosyl-(1->3)-O-6-O-acetyl-4-O-benzoyl-2-deoxy-2-iodo-β-glucopyranosyl-(1->4)-6-O-acetyl-3-O-benzoyl-2-deoxy-2-iodo-1-O-trichloroacetimidyl-α-D-glucopyranose 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: 72.0%

: 545-06-2
trichloroacetonitrile

: C₄₂H₅₆I₂O₁₅Si

: C₄₂H₅₅IO₁₄Si

: O-4-O-(tert-butyldimethyl)silyl-α-rhodinosyl-(1->3)-O-6-O-acetyl-4-O-benzoyl-2-deoxy-2-iodo-β-glucopyranosyl-(1->4)-6-O-acetyl-3-O-benzoyl-2-deoxy-2-iodo-1-O-trichloroacetimidyl-β-D-glucopyranose

: 288859-50-7
O-4-O-(tert-butyldimethyl)silyl-α-rhodinosyl-(1->3)-O-6-O-acetyl-4-O-benzoyl-2-deoxy-2-iodo-β-glucopyranosyl-(1->4)-6-O-acetyl-3-O-benzoyl-2-deoxy-2-iodo-1-O-trichloroacetimidyl-α-D-glucopyranose

Guidance literature:: With sodium hydride; In tetrahydrofuran; at 0 ℃; for 0.5h;
DOI:10.1021/ja000743k

Reference yield:

: O-4-O-(tert-butyldimethyl)silyl-α-rhodinosyl-(1->3)-O-6-O-acetyl-4-O-benzoyl-2-deoxy-2-iodo-β-D-glucopyranosyl-(1->4)-1,6-di-O-acetyl-3-O-benzoyl-2-deoxy-2-iodo-D-glucopyranose

: 288859-50-7
O-4-O-(tert-butyldimethyl)silyl-α-rhodinosyl-(1->3)-O-6-O-acetyl-4-O-benzoyl-2-deoxy-2-iodo-β-glucopyranosyl-(1->4)-6-O-acetyl-3-O-benzoyl-2-deoxy-2-iodo-1-O-trichloroacetimidyl-α-D-glucopyranose

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NH₂NH₂ / methanol; diethyl ether / 0.42 h / 23 °C

2: 72 percent / NaH / tetrahydrofuran / 0.5 h / 0 °C

With sodium hydride; hydrazine hydrate; In tetrahydrofuran; methanol; diethyl ether; 1: Deacetylation / 2: Addition;
DOI:10.1021/ja000743k