Technology Process of (2R,3R,4R)-1-O-benzyl-2,3-O-isopropylidene-5-(4-methoxyphenyl)pentane-1,2,3,4-tetrol
There total 7 articles about (2R,3R,4R)-1-O-benzyl-2,3-O-isopropylidene-5-(4-methoxyphenyl)pentane-1,2,3,4-tetrol which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
1-bromo-4-methoxy-benzene;
With
iodine; magnesium;
In
tetrahydrofuran;
1-O-benzyl-2,3-O-isopropylidene-4-oxiranyl-D-arabinitol;
With
copper(l) iodide;
In
tetrahydrofuran;
at 0 - 20 ℃;
DOI:10.1016/j.tetasy.2005.08.039
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: 860 mg / potassium carbonate / methanol / 0.5 h / 20 °C
2.1: magnesium; iodine / tetrahydrofuran
2.2: 86 percent / copper(I) iodide / tetrahydrofuran / 0 - 20 °C
With
iodine; potassium carbonate; magnesium;
In
tetrahydrofuran; methanol;
2.2: Crignard reaction;
DOI:10.1016/j.tetasy.2005.08.039
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: 84 percent / sodium hydride / dimethylformamide / 20 °C
2.1: 84 percent / acetic acid / H2O / 20 °C
3.1: triethylamine / CH2Cl2 / 16 h / 20 °C
4.1: 860 mg / potassium carbonate / methanol / 0.5 h / 20 °C
5.1: magnesium; iodine / tetrahydrofuran
5.2: 86 percent / copper(I) iodide / tetrahydrofuran / 0 - 20 °C
With
iodine; sodium hydride; potassium carbonate; magnesium; acetic acid; triethylamine;
In
tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
5.2: Crignard reaction;
DOI:10.1016/j.tetasy.2005.08.039