Technology Process of (2'S,3'S,4'R)-1-(2,3,4,6-tetra-O-benzyl-α-C-D-galactopyranosyl)-2-(3',4'-O-isopropylidene-2'-O-(para-methoxybenzyl)-D-ribo-heptadec-5',6'-enyl)-acetylene
There total 8 articles about (2'S,3'S,4'R)-1-(2,3,4,6-tetra-O-benzyl-α-C-D-galactopyranosyl)-2-(3',4'-O-isopropylidene-2'-O-(para-methoxybenzyl)-D-ribo-heptadec-5',6'-enyl)-acetylene 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:
-
n-tridecyltriphenylphosphonium bromide;
With
n-butyllithium;
In
tetrahydrofuran;
at -40 - -5 ℃;
(2'S,3'S,4'S)-1-(2,3,4,6-tetra-O-benzyl-α-C-D-galactopyranosyl)-2-(3',4'-O-isopropylidene-2'-O-(para-methoxybenzyl)-D-ribo-5'-carbaldehyde)-acetylene;
In
tetrahydrofuran;
at -5 - 20 ℃;
DOI:10.1016/j.bmcl.2011.02.044
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: dmap; triethylamine / dichloromethane / 0 - 20 °C
2.1: 1H-imidazole; tetra-(n-butyl)ammonium iodide; sodium hydride / tetrahydrofuran; N,N-dimethyl-formamide / 0 - 20 °C
3.1: n-butyllithium / diethyl ether / -78 - 0 °C
3.2: 1 h / 0 °C
4.1: sodium hydride / N,N-dimethyl-formamide / 0 - 20 °C
5.1: ammonium fluoride / methanol / 3 h / Reflux
6.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 1 h / -78 °C
6.2: 1.5 h / -78 - 20 °C
7.1: n-butyllithium / tetrahydrofuran / -40 - -5 °C
7.2: -5 - 20 °C
With
1H-imidazole; dmap; ammonium fluoride; n-butyllithium; oxalyl dichloride; tetra-(n-butyl)ammonium iodide; sodium hydride; dimethyl sulfoxide; triethylamine;
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane; N,N-dimethyl-formamide;
6.2: Swern oxidation / 7.2: Wittig reaction;
DOI:10.1016/j.bmcl.2011.02.044
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: n-butyllithium / diethyl ether / -78 - 0 °C
1.2: 1 h / 0 °C
2.1: sodium hydride / N,N-dimethyl-formamide / 0 - 20 °C
3.1: ammonium fluoride / methanol / 3 h / Reflux
4.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 1 h / -78 °C
4.2: 1.5 h / -78 - 20 °C
5.1: n-butyllithium / tetrahydrofuran / -40 - -5 °C
5.2: -5 - 20 °C
With
ammonium fluoride; n-butyllithium; oxalyl dichloride; sodium hydride; dimethyl sulfoxide;
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane; N,N-dimethyl-formamide;
4.2: Swern oxidation / 5.2: Wittig reaction;
DOI:10.1016/j.bmcl.2011.02.044
