Technology Process of (2S,3R)-methyl 3-(4-(2-(tert-butyldimethylsilyloxy)ethyl)phenyl)-2,3-dihydroxypropanoate
There total 6 articles about (2S,3R)-methyl 3-(4-(2-(tert-butyldimethylsilyloxy)ethyl)phenyl)-2,3-dihydroxypropanoate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
hydroquinidine 1 4-phthalazinediyl diether; potassium dioxotetrahydroxoosmate(VI); methanesulfonamide; water; potassium carbonate; potassium hexacyanoferrate(III);
In
tert-butyl alcohol;
at 0 - 20 ℃;
stereoselective reaction;
Inert atmosphere;
DOI:10.1002/chem.201101978
- Guidance literature:
-
Multi-step reaction with 2 steps
1: dichloromethane / 20 °C / Inert atmosphere
2: hydroquinidine 1 4-phthalazinediyl diether; potassium dioxotetrahydroxoosmate(VI); methanesulfonamide; water; potassium carbonate; potassium hexacyanoferrate(III) / tert-butyl alcohol / 0 - 20 °C / Inert atmosphere
With
hydroquinidine 1 4-phthalazinediyl diether; potassium dioxotetrahydroxoosmate(VI); methanesulfonamide; water; potassium carbonate; potassium hexacyanoferrate(III);
In
dichloromethane; tert-butyl alcohol;
1: Wittig reaction / 2: Sharpless dihydroxylation;
DOI:10.1002/chem.201101978
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: 1H-imidazole / dichloromethane / 1 h / 20 °C / Inert atmosphere; Cooling with water bath
2.1: n-butyllithium / tetrahydrofuran; hexane / 1 h / -90 - -80 °C / Inert atmosphere
2.2: 0.5 h / -100 - -10 °C / Inert atmosphere
3.1: dichloromethane / 20 °C / Inert atmosphere
4.1: hydroquinidine 1 4-phthalazinediyl diether; potassium dioxotetrahydroxoosmate(VI); methanesulfonamide; water; potassium carbonate; potassium hexacyanoferrate(III) / tert-butyl alcohol / 0 - 20 °C / Inert atmosphere
With
1H-imidazole; hydroquinidine 1 4-phthalazinediyl diether; n-butyllithium; potassium dioxotetrahydroxoosmate(VI); methanesulfonamide; water; potassium carbonate; potassium hexacyanoferrate(III);
In
tetrahydrofuran; hexane; dichloromethane; tert-butyl alcohol;
2.2: Wittig reaction / 3.1: Wittig reaction / 4.1: Sharpless dihydroxylation;
DOI:10.1002/chem.201101978