Technology Process of C56H91N7O16Si
There total 3 articles about C56H91N7O16Si 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:
-
C42H69N5O14; toluene-4-sulfonic acid;
In
methanol;
at 20 ℃;
for 5h;
With
Dess-Martin periodane;
In
dichloromethane;
at 20 ℃;
for 2h;
6-benzyloxycarbonylamino-2-L-amino-hexanoic acid trimethylsilyl ethyl ester;
With
sodium tris(acetoxy)borohydride; N-ethyl-N,N-diisopropylamine;
In
1,2-dichloro-ethane;
at 20 ℃;
for 12h;
Further stages.;
DOI:10.1021/ja005886l
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: DCC; DMAP / CH2Cl2 / 22 h / 20 °C
1.2: 95 percent / TFA / CH2Cl2 / 1.5 h / 20 °C
2.1: methanol / 5 h / 20 °C
2.2: Dess-Martin reagent / CH2Cl2 / 2 h / 20 °C
2.3: sodium triacetoxy-borohydride; diisopropylethylamine / 1,2-dichloro-ethane / 12 h / 20 °C
With
dmap; dicyclohexyl-carbodiimide;
In
methanol; dichloromethane;
DOI:10.1021/ja005886l
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: DCC; DMAP / CH2Cl2 / 22 h / 20 °C
1.2: 95 percent / TFA / CH2Cl2 / 1.5 h / 20 °C
2.1: methanol / 5 h / 20 °C
2.2: Dess-Martin reagent / CH2Cl2 / 2 h / 20 °C
2.3: sodium triacetoxy-borohydride; diisopropylethylamine / 1,2-dichloro-ethane / 12 h / 20 °C
With
dmap; dicyclohexyl-carbodiimide;
In
methanol; dichloromethane;
DOI:10.1021/ja005886l