Technology Process of C23H32O7
There total 1 articles about C23H32O7 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
tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride;
In
dichloromethane;
for 2h;
Reflux;
DOI:10.1021/ol2009686
- Guidance literature:
-
With
water; acetic acid;
at 20 ℃;
for 7h;
regioselective reaction;
DOI:10.1021/ol2009686
- Guidance literature:
-
Multi-step reaction with 10 steps
1.1: water; acetic acid / 7 h / 20 °C
2.1: sodium periodate; silica gel / dichloromethane / 0.5 h / 20 °C
3.1: triethylamine / toluene / 2 h / Reflux
3.2: 2 h / 20 °C
4.1: 2,4,6-trimethyl-pyridine / dichloromethane / 1 h / -78 °C
5.1: potassium carbonate / methanol / 0.17 h / 20 °C
6.1: hydrogen; acetic acid / methanol / 7 h / 20 - 60 °C
7.1: dmap; triethylamine / dichloromethane / 2 h / 0 °C
7.2: 1 h / 0 - 20 °C
8.1: hydrogen / methanol / 7 h / 50 °C
9.1: methanesulfonyl chloride; triethylamine / dichloromethane / 49 h / 0 - 70 °C / sealed tube
10.1: hydrogen / methanol / 14 h / 20 °C
With
2,4,6-trimethyl-pyridine; dmap; sodium periodate; water; hydrogen; silica gel; potassium carbonate; acetic acid; methanesulfonyl chloride; triethylamine;
In
methanol; dichloromethane; toluene;
DOI:10.1021/ol2009686