Technology Process of C38H42BrNO3
There total 5 articles about C38H42BrNO3 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
dmap; triethylamine;
In
dichloromethane;
at 0 - 20 ℃;
Inert atmosphere;
DOI:10.1021/ol2017966
- Guidance literature:
-
Multi-step reaction with 4 steps
1: dmap; triethylamine / dichloromethane / 0 - 20 °C / Inert atmosphere
2: iodine; sodium hydrogencarbonate / acetonitrile / 2.17 h / 0 °C / Inert atmosphere; Darkness
3: ammonia / tetrahydrofuran / -78 - 20 °C / Inert atmosphere
4: dmap; triethylamine / dichloromethane / 0 - 20 °C / Inert atmosphere
With
dmap; ammonia; iodine; sodium hydrogencarbonate; triethylamine;
In
tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/ol2017966
- Guidance literature:
-
Multi-step reaction with 5 steps
1: lithium aluminium tetrahydride / tetrahydrofuran; toluene / 24 h / Inert atmosphere; Reflux
2: dmap; triethylamine / dichloromethane / 0 - 20 °C / Inert atmosphere
3: iodine; sodium hydrogencarbonate / acetonitrile / 2.17 h / 0 °C / Inert atmosphere; Darkness
4: ammonia / tetrahydrofuran / -78 - 20 °C / Inert atmosphere
5: dmap; triethylamine / dichloromethane / 0 - 20 °C / Inert atmosphere
With
dmap; lithium aluminium tetrahydride; ammonia; iodine; sodium hydrogencarbonate; triethylamine;
In
tetrahydrofuran; dichloromethane; toluene; acetonitrile;
DOI:10.1021/ol2017966
