Technology Process of N-isobutyroyl-5’-carboxy-2’,3’-di-O-(carbobenzyloxy)guanosine
There total 4 articles about N-isobutyroyl-5’-carboxy-2’,3’-di-O-(carbobenzyloxy)guanosine 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
2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene;
In
diethyl ether; water; acetone; acetonitrile;
at 25 ℃;
DOI:10.1016/j.bmcl.2013.07.030
- Guidance literature:
-
Multi-step reaction with 3 steps
1: dmap / dichloromethane / 72 h / 20 °C
2: trichloroacetic acid / dichloromethane / 0.25 h / 20 °C
3: 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene / acetone; acetonitrile; water; diethyl ether / 25 °C
With
dmap; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene; trichloroacetic acid;
In
diethyl ether; dichloromethane; water; acetone; acetonitrile;
DOI:10.1016/j.bmcl.2013.07.030
- Guidance literature:
-
Multi-step reaction with 2 steps
1: trichloroacetic acid / dichloromethane / 0.25 h / 20 °C
2: 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene / acetone; acetonitrile; water; diethyl ether / 25 °C
With
2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene; trichloroacetic acid;
In
diethyl ether; dichloromethane; water; acetone; acetonitrile;
DOI:10.1016/j.bmcl.2013.07.030