Technology Process of C36H46N2O9
There total 8 articles about C36H46N2O9 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
C36H46N2O9;
With
mercuric triflate; sodium hydrogencarbonate;
In
dichloromethane;
at -20 ℃;
for 10.5h;
Inert atmosphere;
Cooling with ice;
With
lithium borohydride; triethyl borane;
In
tetrahydrofuran; dichloromethane;
at -78 ℃;
for 0.5h;
Inert atmosphere;
DOI:10.1039/c3cc42365d
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: 1H-imidazole; triphenylphosphine; iodine / dichloromethane / 2 h / Cooling with ice; Inert atmosphere
2.1: caesium carbonate / N,N-dimethyl-formamide / 0.5 h / Cooling with ice; Inert atmosphere
2.2: 8 h / 20 °C / Inert atmosphere
2.3: 3.33 h / 20 °C / Inert atmosphere
3.1: C15H26Cl2CuN2O2; triethylamine / tetrahydrofuran / 3 h / 20 °C / Inert atmosphere
4.1: Dess-Martin periodane / dichloromethane / 5 h / Cooling with ice; Inert atmosphere
5.1: dichloromethane / 15 h / 50 °C / Inert atmosphere
6.1: sodium hydrogencarbonate; mercuric triflate / dichloromethane / 10.5 h / -20 °C / Inert atmosphere; Cooling with ice
6.2: 0.5 h / -78 °C / Inert atmosphere
With
1H-imidazole; C15H26Cl2CuN2O2; iodine; mercuric triflate; sodium hydrogencarbonate; caesium carbonate; Dess-Martin periodane; triethylamine; triphenylphosphine;
In
tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
4.1: |Dess-Martin Oxidation / 5.1: |Wittig Olefination;
DOI:10.1039/c3cc42365d
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: C15H26Cl2CuN2O2; triethylamine / tetrahydrofuran / 3 h / 20 °C / Inert atmosphere
2.1: Dess-Martin periodane / dichloromethane / 5 h / Cooling with ice; Inert atmosphere
3.1: dichloromethane / 15 h / 50 °C / Inert atmosphere
4.1: sodium hydrogencarbonate; mercuric triflate / dichloromethane / 10.5 h / -20 °C / Inert atmosphere; Cooling with ice
4.2: 0.5 h / -78 °C / Inert atmosphere
With
C15H26Cl2CuN2O2; mercuric triflate; sodium hydrogencarbonate; Dess-Martin periodane; triethylamine;
In
tetrahydrofuran; dichloromethane;
2.1: |Dess-Martin Oxidation / 3.1: |Wittig Olefination;
DOI:10.1039/c3cc42365d