Technology Process of (22R,25R)-3β-O-tert-butyldiphenylsilyloxy-26-hydroxy-5-furosten
There total 2 articles about (22R,25R)-3β-O-tert-butyldiphenylsilyloxy-26-hydroxy-5-furosten which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
lithium aluminium tetrahydride; aluminium trichloride;
In
diethyl ether;
at 20 ℃;
DOI:10.1002/ejoc.200300290
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 96 percent / imidazole / dimethylformamide
2: 47 percent / LiAlH4; AlCl3 / diethyl ether / 20 °C
With
1H-imidazole; lithium aluminium tetrahydride; aluminium trichloride;
In
diethyl ether; N,N-dimethyl-formamide;
DOI:10.1002/ejoc.200300290
- Guidance literature:
-
Multi-step reaction with 9 steps
1.1: Jones reagent / acetone / 3 h / 0 °C / Inert atmosphere
2.1: lithium bromide; trifluoroacetic anhydride / dichloromethane; acetonitrile / 24 h / 20 °C / Inert atmosphere
3.1: palladium 10% on activated carbon; hydrogen; sodium acetate / methanol; dichloromethane / 7 h / 30 °C / 7600.51 Torr
4.1: potassium carbonate / methanol / 3 h / 50 °C / Inert atmosphere
4.2: 20 °C / Inert atmosphere
5.1: triethylamine; dmap / dichloromethane / 20 °C / Inert atmosphere
6.1: sodium azide / N,N-dimethyl-formamide / 6 h / 60 °C / Inert atmosphere
7.1: sodium hydrogencarbonate; Dess-Martin periodane / dichloromethane / 2 h / 20 °C / Inert atmosphere
8.1: hydrogen / methanol / 4 h / 40 °C
9.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 50 °C / Inert atmosphere
With
dmap; Jones reagent; sodium azide; palladium 10% on activated carbon; tetrabutyl ammonium fluoride; hydrogen; sodium acetate; sodium hydrogencarbonate; potassium carbonate; Dess-Martin periodane; triethylamine; trifluoroacetic anhydride; lithium bromide;
In
tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; acetone; acetonitrile;
1.1: |Jones Oxidation;
DOI:10.1021/acs.orglett.0c00747