Technology Process of C34H49NO6Si
There total 5 articles about C34H49NO6Si 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
N-ethyl-N,N-diisopropylamine;
In
dichloromethane;
at 0 ℃;
for 3h;
Inert atmosphere;
DOI:10.1021/jo300225z
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: quinoline; hydrogen / ethyl acetate / 2 h
2.1: oxalyl dichloride; dimethyl sulfoxide; triethylamine / dichloromethane / -78 - 0 °C / Inert atmosphere
3.1: di-n-butylboryl trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / -78 - 20 °C / Inert atmosphere
3.2: 3 h / -78 °C / Inert atmosphere
4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 0 °C / Inert atmosphere
With
quinoline; oxalyl dichloride; di-n-butylboryl trifluoromethanesulfonate; hydrogen; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine;
In
dichloromethane; ethyl acetate;
2.1: Swern oxidation / 3.1: Evans aldol reaction / 3.2: Evans aldol reaction;
DOI:10.1021/jo300225z
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: oxalyl dichloride; dimethyl sulfoxide; triethylamine / dichloromethane / -78 - 0 °C / Inert atmosphere
2.1: di-n-butylboryl trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / -78 - 20 °C / Inert atmosphere
2.2: 3 h / -78 °C / Inert atmosphere
3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 0 °C / Inert atmosphere
With
oxalyl dichloride; di-n-butylboryl trifluoromethanesulfonate; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine;
In
dichloromethane;
1.1: Swern oxidation / 2.1: Evans aldol reaction / 2.2: Evans aldol reaction;
DOI:10.1021/jo300225z
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