Technology Process of (2S,3R)-2-(tert-butyloxycarbonylamino)-3-hydroxy-1-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)pent-4-ene
There total 6 articles about (2S,3R)-2-(tert-butyloxycarbonylamino)-3-hydroxy-1-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)pent-4-ene 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
tetrabutyl ammonium fluoride;
In
tetrahydrofuran;
at 20 ℃;
for 24h;
DOI:10.1021/jm900290r
- Guidance literature:
-
Multi-step reaction with 2 steps
1: silver perchlorate; titanium tetrachloride / tetrahydrofuran; diethyl ether / 0.33 h / 0 °C
2: tetrabutyl ammonium fluoride / tetrahydrofuran / 16 h / 20 °C
With
tetrabutyl ammonium fluoride; silver perchlorate; titanium tetrachloride;
In
tetrahydrofuran; diethyl ether;
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: tin(IV) chloride / benzene / 2 h / 20 °C / Heating / reflux
2.1: methanol; sodium methylate / 1 h
3.1: sodium hydride / N,N-dimethyl-formamide / 0.25 h / 0 °C
3.2: 3 h / 20 °C
4.1: N-Bromosuccinimide; diethylamino-sulfur trifluoride / dichloromethane / 0.5 h / -15 °C
5.1: silver perchlorate; titanium tetrachloride / tetrahydrofuran; diethyl ether / 0.33 h / 0 °C
6.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 16 h / 20 °C
With
methanol; N-Bromosuccinimide; diethylamino-sulfur trifluoride; tetrabutyl ammonium fluoride; sodium methylate; silver perchlorate; titanium tetrachloride; tin(IV) chloride; sodium hydride;
In
tetrahydrofuran; diethyl ether; dichloromethane; N,N-dimethyl-formamide; benzene;