1,3,2',6'-Tetra-N-(benzyloxycarbonyl)-2'',3'',5''-tri-O-benzoyl-6,3',4'-tri-O-benzylribostamycin

Base Information

Chemical Name:1,3,2',6'-Tetra-N-(benzyloxycarbonyl)-2'',3'',5''-tri-O-benzoyl-6,3',4'-tri-O-benzylribostamycin
CAS No.:78763-89-0
Molecular Formula:C₉₁H₈₈N₄O₂₁
Molecular Weight:1573.71
Hs Code.:

Synonyms:1,3,2',6'-Tetra-N-(benzyloxycarbonyl)-2'',3'',5''-tri-O-benzoyl-6,3',4'-tri-O-benzylribostamycin

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1,3,2',6'-Tetra-N-(benzyloxycarbonyl)-2'',3'',5''-tri-O-benzoyl-6,3',4'-tri-O-benzylribostamycin

Chemical Property:

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Technology Process of 1,3,2',6'-Tetra-N-(benzyloxycarbonyl)-2'',3'',5''-tri-O-benzoyl-6,3',4'-tri-O-benzylribostamycin

There total 1 articles about 1,3,2',6'-Tetra-N-(benzyloxycarbonyl)-2'',3'',5''-tri-O-benzoyl-6,3',4'-tri-O-benzylribostamycin 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: 35.0%

: 78763-85-6
1,3,2',6'-Tetra-N-(benzyloxycarbonyl)-6,3',4'-tri-O-benzylneamine

: 5991-01-5
2,3,5-(tri-O-benzoyl)-D-ribofuranosyl chloride

: 78763-89-0
1,3,2',6'-Tetra-N-(benzyloxycarbonyl)-2'',3'',5''-tri-O-benzoyl-6,3',4'-tri-O-benzylribostamycin

Guidance literature:: With calcium sulfate; mercury(II) cyanide; In chloroform; for 72h; Heating;
DOI:10.1021/jo00334a042

Reference yield:

: 78763-89-0
1,3,2',6'-Tetra-N-(benzyloxycarbonyl)-2'',3'',5''-tri-O-benzoyl-6,3',4'-tri-O-benzylribostamycin

: 25546-65-0
ribostamycin

Guidance literature:: With palladium on activated charcoal; hydrogen; sodium methylate; acetic acid; Yield given. Multistep reaction; 1.) MeOH, 3.5 h, 2.) aq. dioxane, 48 h, then water;
DOI:10.1021/jo00334a042