Technology Process of Oxiranemethanol, 2-[2-(4-octylphenyl)ethyl]-, (2S)-
There total 5 articles about Oxiranemethanol, 2-[2-(4-octylphenyl)ethyl]-, (2S)- which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
L-(+)-diisopropyl tartrate; Cumene hydroperoxide;
titanium(IV) isopropylate;
In
dichloromethane;
at -20 ℃;
DOI:10.1016/j.tetlet.2005.11.092
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: n-BuLi / tetrahydrofuran
1.2: 81 percent / H2 / Pd(OH)2/C / methanol
2.1: PCC; NaOAc; molecular sieves / CH2Cl2
2.2: 76 percent / Et3N / CH2Cl2
3.1: 87 percent / NaBH4 / CeCl3 / methanol
4.1: 83 percent / (+)-DIPT; cumene hydroperoxide; MS / Ti(OPr-i)4 / CH2Cl2 / -20 °C
With
sodium tetrahydroborate; n-butyllithium; molecular sieve; L-(+)-diisopropyl tartrate; Cumene hydroperoxide; sodium acetate; pyridinium chlorochromate;
titanium(IV) isopropylate; cerium(III) chloride;
In
tetrahydrofuran; methanol; dichloromethane;
1.1: Wittig reaction / 2.2: Mannich reaction / 4.1: asymmetric Sharpless epoxidation;
DOI:10.1016/j.tetlet.2005.11.092
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 87 percent / NaBH4 / CeCl3 / methanol
2: 83 percent / (+)-DIPT; cumene hydroperoxide; MS / Ti(OPr-i)4 / CH2Cl2 / -20 °C
With
sodium tetrahydroborate; L-(+)-diisopropyl tartrate; Cumene hydroperoxide;
titanium(IV) isopropylate; cerium(III) chloride;
In
methanol; dichloromethane;
2: asymmetric Sharpless epoxidation;
DOI:10.1016/j.tetlet.2005.11.092