Technology Process of (2S,3S,4S,6R,8R)-1-benzyloxy-8-(N-benzyloxycarbonylamino)-3,6-epoxy-2-methyl-4-(phenylseleno)undecane
There total 7 articles about (2S,3S,4S,6R,8R)-1-benzyloxy-8-(N-benzyloxycarbonylamino)-3,6-epoxy-2-methyl-4-(phenylseleno)undecane 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
tin(IV) chloride;
In
dichloromethane;
at 20 ℃;
for 18h;
DOI:10.1039/c2ob26801a
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: n-butyllithium / hexane; tetrahydrofuran / 0.5 h / -78 °C
1.2: 2 h / -78 °C
2.1: 20% palladium hydroxide-activated charcoal; ammonium formate; formic acid / methanol / 3 h / 20 °C
3.1: potassium carbonate / water; diethyl ether / 3.5 h / 0 - 20 °C
4.1: lithium aluminium tetrahydride / diethyl ether / 2.17 h / 0 - 20 °C
5.1: oxalyl dichloride; triethylamine; dimethyl sulfoxide / dichloromethane / 0.5 h / -78 - 20 °C
6.1: tin(IV) chloride / dichloromethane / 0.08 h / -78 °C
6.2: 0.83 h / -78 °C
7.1: tin(IV) chloride / dichloromethane / 18 h / 20 °C
With
lithium aluminium tetrahydride; n-butyllithium; formic acid; oxalyl dichloride; 20% palladium hydroxide-activated charcoal; ammonium formate; tin(IV) chloride; potassium carbonate; dimethyl sulfoxide; triethylamine;
In
tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; water;
DOI:10.1039/c2ob26801a
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: 20% palladium hydroxide-activated charcoal; ammonium formate; formic acid / methanol / 3 h / 20 °C
2.1: potassium carbonate / water; diethyl ether / 3.5 h / 0 - 20 °C
3.1: lithium aluminium tetrahydride / diethyl ether / 2.17 h / 0 - 20 °C
4.1: oxalyl dichloride; triethylamine; dimethyl sulfoxide / dichloromethane / 0.5 h / -78 - 20 °C
5.1: tin(IV) chloride / dichloromethane / 0.08 h / -78 °C
5.2: 0.83 h / -78 °C
6.1: tin(IV) chloride / dichloromethane / 18 h / 20 °C
With
lithium aluminium tetrahydride; formic acid; oxalyl dichloride; 20% palladium hydroxide-activated charcoal; ammonium formate; tin(IV) chloride; potassium carbonate; dimethyl sulfoxide; triethylamine;
In
methanol; diethyl ether; dichloromethane; water;
DOI:10.1039/c2ob26801a