Technology Process of 2,5-anhydro 3,4-di-O-tosyl-D-xylose diisobutyldithioacetal
There total 1 articles about 2,5-anhydro 3,4-di-O-tosyl-D-xylose diisobutyldithioacetal which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 7 steps
1: Br2 / diethyl ether; H2O / 0.25 h
2: 3percent HCl / 2 h / Heating
3: 33 percent / methanolate de sodium / CH2Cl2 / 120 h / 25 °C
4: 88 percent / tetrahydrofuran; hexamethylphosphoric acid triamide / 0 °C
5: 640 mg / pyridine / 0 °C
6: 96 percent / nickel de Raney / ethanol / Heating
7: acide trifluoroacetique aqueux 50percent / CHCl3 / 12 h / 0 °C
With
hydrogenchloride; bromine; sodium methylate; trifluoroacetic acid;
nickel de Raney;
In
tetrahydrofuran; pyridine; N,N,N,N,N,N-hexamethylphosphoric triamide; diethyl ether; ethanol; dichloromethane; chloroform; water;
DOI:10.1016/S0040-4020(01)98931-8
- Guidance literature:
-
Multi-step reaction with 6 steps
1: Br2 / diethyl ether; H2O / 0.25 h
2: 3percent HCl / 2 h / Heating
3: 33 percent / methanolate de sodium / CH2Cl2 / 120 h / 25 °C
4: 88 percent / tetrahydrofuran; hexamethylphosphoric acid triamide / 0 °C
5: 640 mg / pyridine / 0 °C
6: 96 percent / nickel de Raney / ethanol / Heating
With
hydrogenchloride; bromine; sodium methylate;
nickel de Raney;
In
tetrahydrofuran; pyridine; N,N,N,N,N,N-hexamethylphosphoric triamide; diethyl ether; ethanol; dichloromethane; water;
DOI:10.1016/S0040-4020(01)98931-8