Technology Process of methyl 2-O-benzyl-3,4-dideoxy-α-pent-4-enopyranoside
There total 4 articles about methyl 2-O-benzyl-3,4-dideoxy-α-pent-4-enopyranoside 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
DMF dineopentyl acetal;
In
N,N-dimethyl-formamide;
at 200 ℃;
for 2h;
high-pressure vessel;
DOI:10.1021/jo102382r
- Guidance literature:
-
Multi-step reaction with 3 steps
1: acetic acid / tetrahydrofuran; water / 45 °C
2: 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene / dichloromethane; water / 1 h / 20 °C
3: DMF dineopentyl acetal / N,N-dimethyl-formamide / 2 h / 200 °C / high-pressure vessel
With
2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene; DMF dineopentyl acetal; acetic acid;
In
tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1021/jo102382r
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene / dichloromethane; water / 1 h / 20 °C
2: DMF dineopentyl acetal / N,N-dimethyl-formamide / 2 h / 200 °C / high-pressure vessel
With
2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene; DMF dineopentyl acetal;
In
dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1021/jo102382r