(Benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-α-D-mannopyranosid)uronsaeure

Base Information

Chemical Name:(Benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-α-D-mannopyranosid)uronsaeure
CAS No.:95530-21-5
Molecular Formula:C₂₁H₂₃NO₈
Molecular Weight:417.416
Hs Code.:

Synonyms:(Benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-α-D-mannopyranosid)uronsaeure

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Chemical Property of (Benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-α-D-mannopyranosid)uronsaeure

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Technology Process of (Benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-α-D-mannopyranosid)uronsaeure

There total 21 articles about (Benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-α-D-mannopyranosid)uronsaeure 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: 55.0%

: 42890-09-5
Benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-α-D-mannopyranosid

: 95530-21-5
(Benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-α-D-mannopyranosid)uronsaeure

Guidance literature:: With oxygen; sodium hydrogencarbonate; platinum(IV) oxide; In 1,4-dioxane; water; at 80 ℃; for 2.5h;
DOI:10.1016/0008-6215(85)85193-4

Reference yield: 21.0%

: 42890-09-5
Benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-α-D-mannopyranosid

: 43098-12-0
1-O-benzyl-α-D-mannopyranosido-[2,3:4',5']-2'-oxazolidinone

: 95530-21-5
(Benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-α-D-mannopyranosid)uronsaeure

Guidance literature:: With oxygen; potassium hydrogencarbonate; platinum; In 1,4-dioxane; water; at 70 ℃; for 8h; pH=7.0 - 7.5;
DOI:10.1080/00397910701410871

Reference yield:

: 35812-81-8,738518-26-8
Benzyl-2-amino-2-desoxy-α-D-mannopyranosid

: 95530-21-5
(Benzyl-2-<(benzyloxycarbonyl)amino>-2-desoxy-α-D-mannopyranosid)uronsaeure

Guidance literature:: Multi-step reaction with 2 steps

1: 77 percent / K₂CO₃ / dioxane; H₂O / 1 h / Ambient temperature

2: 55 percent / O₂, NaHCO₃ / Adams-catalyst (Pt) / H₂O; dioxane / 2.5 h / 80 °C

With oxygen; sodium hydrogencarbonate; potassium carbonate; platinum(IV) oxide; In 1,4-dioxane; water;
DOI:10.1016/0008-6215(85)85193-4