Technology Process of C55H73NO9
There total 20 articles about C55H73NO9 which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
- Guidance literature:
-
With
water; potassium carbonate;
In
methanol;
at 20 ℃;
Inert atmosphere;
DOI:10.1021/ol2032448
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 1H-imidazole; iodine; triphenylphosphine / diethyl ether; benzene / 0.67 h / 20 °C / Inert atmosphere
2: zinc / ethanol / 0.75 h / Inert atmosphere; Reflux
3: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 2 h / Inert atmosphere; Reflux
4: dichloromethane / 0.5 h / 20 °C / Inert atmosphere
5: water; potassium carbonate / methanol / 20 °C / Inert atmosphere
With
1H-imidazole; tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; water; iodine; potassium carbonate; triphenylphosphine; zinc;
In
methanol; diethyl ether; ethanol; dichloromethane; benzene;
DOI:10.1021/ol2032448
- Guidance literature:
-
Multi-step reaction with 4 steps
1: zinc / ethanol / 0.75 h / Inert atmosphere; Reflux
2: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 2 h / Inert atmosphere; Reflux
3: dichloromethane / 0.5 h / 20 °C / Inert atmosphere
4: water; potassium carbonate / methanol / 20 °C / Inert atmosphere
With
tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; water; potassium carbonate; zinc;
In
methanol; ethanol; dichloromethane;
DOI:10.1021/ol2032448