(2-O-benzoyl-3-O-levulinoyl-β-D-galactopyranosyl)-(1->4)-[(α-L-fucopyranosyl)-(1->3)]-2-O-acetyl-N-decyl-1,5-dideoxy-1,5-imino-D-glucitol

Base Information

Chemical Name:(2-O-benzoyl-3-O-levulinoyl-β-D-galactopyranosyl)-(1->4)-[(α-L-fucopyranosyl)-(1->3)]-2-O-acetyl-N-decyl-1,5-dideoxy-1,5-imino-D-glucitol
CAS No.:418763-58-3
Molecular Formula:C₄₂H₆₅NO₁₇
Molecular Weight:855.975
Hs Code.:

Synonyms:(2-O-benzoyl-3-O-levulinoyl-β-D-galactopyranosyl)-(1->4)-[(α-L-fucopyranosyl)-(1->3)]-2-O-acetyl-N-decyl-1,5-dideoxy-1,5-imino-D-glucitol

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Chemical Property of (2-O-benzoyl-3-O-levulinoyl-β-D-galactopyranosyl)-(1->4)-[(α-L-fucopyranosyl)-(1->3)]-2-O-acetyl-N-decyl-1,5-dideoxy-1,5-imino-D-glucitol

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Technology Process of (2-O-benzoyl-3-O-levulinoyl-β-D-galactopyranosyl)-(1->4)-[(α-L-fucopyranosyl)-(1->3)]-2-O-acetyl-N-decyl-1,5-dideoxy-1,5-imino-D-glucitol

There total 5 articles about (2-O-benzoyl-3-O-levulinoyl-β-D-galactopyranosyl)-(1->4)-[(α-L-fucopyranosyl)-(1->3)]-2-O-acetyl-N-decyl-1,5-dideoxy-1,5-imino-D-glucitol 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: 80.0%

: 112-31-2
caprinaldehyde

: 418763-56-1
(2-O-benzoyl-3-O-levulinoyl-β-D-galactopyranosyl)-(1->4)-[α-L-fucopyranosyl-(1->3)]-2-O-acetyl-1,5-dideoxy-1,5-imino-D-glucitol

: 418763-58-3
(2-O-benzoyl-3-O-levulinoyl-β-D-galactopyranosyl)-(1->4)-[(α-L-fucopyranosyl)-(1->3)]-2-O-acetyl-N-decyl-1,5-dideoxy-1,5-imino-D-glucitol

Guidance literature:: With hydrogen; palladium hydroxide - carbon; In tetrahydrofuran; ethyl acetate;
DOI:10.1081/CAR-100108657

Reference yield:

: 178962-70-4
methyl 2-O-benzoyl-4,6-O-benzylidene-3-O-levulinoyl-1-thio-β-D-galactopyranoside

: 418763-58-3
(2-O-benzoyl-3-O-levulinoyl-β-D-galactopyranosyl)-(1->4)-[(α-L-fucopyranosyl)-(1->3)]-2-O-acetyl-N-decyl-1,5-dideoxy-1,5-imino-D-glucitol

Guidance literature:: Multi-step reaction with 4 steps

1: 70 percent / molecular sieves 4 Angstroem; N-iodosuccinimide; TMSOTf / CH₂Cl₂ / 0 - 20 °C

2: 89 percent / AcOH / H₂O / 45 °C

3: 79 percent / H₂; AcOH / Pd

4: 80 percent / H₂ / Pd(OH)2-C / ethyl acetate; tetrahydrofuran

With N-iodo-succinimide; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; hydrogen; acetic acid; palladium hydroxide - carbon; palladium; In tetrahydrofuran; dichloromethane; water; ethyl acetate;
DOI:10.1081/CAR-100108657

Reference yield:

: 173273-81-9
(2-O-benzoyl-3-O-levulinoyl-β-D-galactopyranosyl)-(1->4)-[(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)]-2-O-acetyl-6-O-benzyl-N-benzyloxycarbonyl-1,5-dideoxy-1,5-imino-D-glucitol

: 418763-58-3
(2-O-benzoyl-3-O-levulinoyl-β-D-galactopyranosyl)-(1->4)-[(α-L-fucopyranosyl)-(1->3)]-2-O-acetyl-N-decyl-1,5-dideoxy-1,5-imino-D-glucitol

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / H₂; AcOH / Pd

2: 80 percent / H₂ / Pd(OH)2-C / ethyl acetate; tetrahydrofuran

With hydrogen; acetic acid; palladium hydroxide - carbon; palladium; In tetrahydrofuran; ethyl acetate;
DOI:10.1081/CAR-100108657