Technology Process of 2,4-Di-O-Acetyl-1,3-O-benzyliden-α-D-tagatopyranose
There total 7 articles about 2,4-Di-O-Acetyl-1,3-O-benzyliden-α-D-tagatopyranose which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 6 steps
1: BaO, Ba(OH)2*8H2O / dimethylformamide / 48 h
2: LiAlH4 / tetrahydrofuran / 24 h / Ambient temperature
3: 98 percent / RuO2, K2CO3, NaIO4 / CH2Cl2; H2O / 7 h
4: LiAlH4 / tetrahydrofuran / 0 degC to room temp.
5: 52 percent / 90percent CF3COOH / 0.17 h / Ambient temperature
6: pyridine / 48 h / 60 °C
With
ruthenium(IV) oxide; barium dihydroxide; sodium periodate; lithium aluminium tetrahydride; potassium carbonate; trifluoroacetic acid; barium(II) oxide;
In
tetrahydrofuran; pyridine; dichloromethane; water; N,N-dimethyl-formamide;
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 98 percent / RuO2, K2CO3, NaIO4 / CH2Cl2; H2O / 7 h
2: LiAlH4 / tetrahydrofuran / 0 degC to room temp.
3: 52 percent / 90percent CF3COOH / 0.17 h / Ambient temperature
4: pyridine / 48 h / 60 °C
With
ruthenium(IV) oxide; sodium periodate; lithium aluminium tetrahydride; potassium carbonate; trifluoroacetic acid;
In
tetrahydrofuran; pyridine; dichloromethane; water;
- Guidance literature:
-
Multi-step reaction with 3 steps
1: LiAlH4 / tetrahydrofuran / 0 degC to room temp.
2: 52 percent / 90percent CF3COOH / 0.17 h / Ambient temperature
3: pyridine / 48 h / 60 °C
With
lithium aluminium tetrahydride; trifluoroacetic acid;
In
tetrahydrofuran; pyridine;