Technology Process of C39H52O4
There total 16 articles about C39H52O4 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 11 steps
1: Sharpless oxidation
3: 60 percent / imidazole / dimethylformamide / Ambient temperature
4: LDA / tetrahydrofuran / -40 °C
5: 91 percent / LiAlH4 / tetrahydrofuran / 1.5 h / -50 °C
6: pyridine / 36 h / Ambient temperature
7: Pr2NEt / 24 h / Ambient temperature
8: n-Bu4NF / tetrahydrofuran / 3.5 h / 0 °C
9: n-Bu3P / pyridine / 24 h / Ambient temperature
10: 99.7 percent / m-chloroperbenzoic acid / CH2Cl2 / 14 h / -20 - -10 °C
With
1H-imidazole; lithium aluminium tetrahydride; dipropylethylamine; tributylphosphine; tetrabutyl ammonium fluoride; 3-chloro-benzenecarboperoxoic acid; lithium diisopropyl amide;
In
tetrahydrofuran; pyridine; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(01)80742-5
- Guidance literature:
-
Multi-step reaction with 2 steps
1: PCC / CH2Cl2 / 0.5 h / 0 - 25 °C
With
pyridinium chlorochromate;
In
dichloromethane;
DOI:10.1016/S0040-4039(01)80742-5
- Guidance literature:
-
Multi-step reaction with 6 steps
1: pyridine / 36 h / Ambient temperature
2: Pr2NEt / 24 h / Ambient temperature
3: n-Bu4NF / tetrahydrofuran / 3.5 h / 0 °C
4: n-Bu3P / pyridine / 24 h / Ambient temperature
5: 99.7 percent / m-chloroperbenzoic acid / CH2Cl2 / 14 h / -20 - -10 °C
With
dipropylethylamine; tributylphosphine; tetrabutyl ammonium fluoride; 3-chloro-benzenecarboperoxoic acid;
In
tetrahydrofuran; pyridine; dichloromethane;
DOI:10.1016/S0040-4039(01)80742-5