Technology Process of 2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl-(1->3)-2,4,6-tri-O-benzyl-α,β-D-galactopyranosyl fluoride
There total 7 articles about 2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl-(1->3)-2,4,6-tri-O-benzyl-α,β-D-galactopyranosyl fluoride which
guide to synthetic route it.
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synthetic route:
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(3R,4S,5S,6R)-3,5-Bis-benzyloxy-6-benzyloxymethyl-4-((2S,3R,4S,5S,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-ol
- Guidance literature:
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With
diethylamino-sulfur trifluoride;
In
tetrahydrofuran;
at 20 ℃;
for 1h;
DOI:10.1016/S0040-4020(02)01359-5
- Guidance literature:
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Multi-step reaction with 3 steps
1: 67 percent / NaH / dimethylformamide / 12 h / -15 - 20 °C
2: PdCl2; sodium acetate / acetic acid; H2O / 18 h / 20 °C
3: 160 mg / (diethylamino)sulfur trifluoride / tetrahydrofuran / 1 h / 20 °C
With
diethylamino-sulfur trifluoride; sodium acetate; sodium hydride; palladium dichloride;
In
tetrahydrofuran; water; acetic acid; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(02)01359-5
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: pyridinium p-toluenesulfonate / acetonitrile / 0.17 h
1.2: 100 percent / acetic acid / acetonitrile; H2O / 1.5 h
2.1: 96 percent / trimethylsilyl trifluoromethanesulfonate; molecular sieves 4 Angstroem / CH2Cl2 / 2 h / -15 °C
3.1: sodium methoxide / methanol / 1 h / 20 °C
4.1: 67 percent / NaH / dimethylformamide / 12 h / -15 - 20 °C
5.1: PdCl2; sodium acetate / acetic acid; H2O / 18 h / 20 °C
6.1: 160 mg / (diethylamino)sulfur trifluoride / tetrahydrofuran / 1 h / 20 °C
With
diethylamino-sulfur trifluoride; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; sodium methylate; sodium acetate; pyridinium p-toluenesulfonate; sodium hydride; palladium dichloride;
In
tetrahydrofuran; methanol; dichloromethane; water; acetic acid; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/S0040-4020(02)01359-5