Technology Process of [1'-13C]-2',3',5'-tri-O-benzoyl-N4-benzoylcytidine
There total 7 articles about [1'-13C]-2',3',5'-tri-O-benzoyl-N4-benzoylcytidine which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 2 steps
1: (NH4)2SO4 / 14 h / Heating
2: 86 percent / TMSOTf / 1,2-dichloro-ethane / 5.5 h / 20 - 45 °C
With
ammonium sulfate; trimethylsilyl trifluoromethanesulfonate;
In
1,2-dichloro-ethane;
DOI:10.1016/S0008-6215(00)00327-X
- Guidance literature:
-
Multi-step reaction with 5 steps
1: H2SO4 / 0 °C
2: pyridine / 0 °C
3: 95 percent / BF3*Et2O / CH2Cl2 / 1 h / 0 °C
4: 95 percent / m-CPBA, NaHCO3 / CH2Cl2 / 1 h / 0 °C
5: 1) hexamethyldisilazane, 2) TMSOTf / 1) reflux, 2) 1,2-dichloroethane, r.t.
With
pyridine; trimethylsilyl trifluoromethanesulfonate; sulfuric acid; boron trifluoride diethyl etherate; sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid; 1,1,1,3,3,3-hexamethyl-disilazane;
In
dichloromethane;
DOI:10.1016/S0040-4039(00)79089-7
- Guidance literature:
-
Multi-step reaction with 3 steps
1: BF3*Et2O / CH2Cl2
2: 95 percent / m-CPBA, NaHCO3 / CH2Cl2 / 1 h / 0 °C
3: 1) hexamethyldisilazane, 2) TMSOTf / 1) reflux, 2) 1,2-dichloroethane, r.t.
With
trimethylsilyl trifluoromethanesulfonate; boron trifluoride diethyl etherate; sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid; 1,1,1,3,3,3-hexamethyl-disilazane;
In
dichloromethane;
DOI:10.1016/S0040-4039(00)79089-7