Technology Process of (R)-1-((2R,5R)-5-(phenylethynyl)tetrahydrofuran-2-yl)propan-1-ol
There total 6 articles about (R)-1-((2R,5R)-5-(phenylethynyl)tetrahydrofuran-2-yl)propan-1-ol which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
1,1'-bis-(diphenylphosphino)ferrocene; boric acid; palladium diacetate;
In
1,4-dioxane;
at 50 ℃;
for 0.5h;
optical yield given as %de;
diastereoselective reaction;
Inert atmosphere;
DOI:10.1002/anie.201105720
- Guidance literature:
-
Multi-step reaction with 3 steps
1: pyridine / dichloromethane / 0 °C / Inert atmosphere
2: AD-mix-β; methanesulfonamide / water; tert-butyl alcohol / 0 °C
3: 1,1'-bis-(diphenylphosphino)ferrocene; boric acid; palladium diacetate / 1,4-dioxane / 0.5 h / 50 °C / Inert atmosphere
With
pyridine; 1,1'-bis-(diphenylphosphino)ferrocene; methanesulfonamide; AD-mix-β; boric acid; palladium diacetate;
In
1,4-dioxane; dichloromethane; water; tert-butyl alcohol;
2: Sharpless dihydroxylation;
DOI:10.1002/anie.201105720
- Guidance literature:
-
Multi-step reaction with 4 steps
1: Noyori's catalyst / 20 °C / Inert atmosphere
2: pyridine / dichloromethane / 0 °C / Inert atmosphere
3: AD-mix-β; methanesulfonamide / water; tert-butyl alcohol / 0 °C
4: 1,1'-bis-(diphenylphosphino)ferrocene; boric acid; palladium diacetate / 1,4-dioxane / 0.5 h / 50 °C / Inert atmosphere
With
pyridine; 1,1'-bis-(diphenylphosphino)ferrocene; Noyori's catalyst; methanesulfonamide; AD-mix-β; boric acid; palladium diacetate;
In
1,4-dioxane; dichloromethane; water; tert-butyl alcohol;
1: Noyori reduction / 3: Sharpless dihydroxylation;
DOI:10.1002/anie.201105720