Technology Process of 1''',2''',5'''-triepisilvestrol
There total 6 articles about 1''',2''',5'''-triepisilvestrol which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
- Guidance literature:
-
With
tetrabutyl ammonium fluoride;
In
tetrahydrofuran;
at 0 - 20 ℃;
for 1h;
DOI:10.1021/np300376f
- Guidance literature:
-
Multi-step reaction with 3 steps
1: hydrogen; 20% Pd/C / ethanol / 3 h
2: triphenylphosphine; azodicarboxylic acid bis(2-methoxyethyl) ester / toluene / 48 h / 0 °C / Molecular sieve
3: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 0 - 20 °C
With
azodicarboxylic acid bis(2-methoxyethyl) ester; 20% Pd/C; tetrabutyl ammonium fluoride; hydrogen; triphenylphosphine;
In
tetrahydrofuran; ethanol; toluene;
2: |Mitsunobu Displacement;
DOI:10.1021/np300376f
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: chloroform; 2,2,2-trifluoroethanol / 15 h / -5 °C / Inert atmosphere; UV-irradiation
2.1: sodium methylate / methanol / 0.67 h / Reflux
2.2: 19 h / Inert atmosphere
3.1: 5 μm Phenomenex Lux Cellulose-1 semipreparative column / acetonitrile; water / Resolution of racemate
4.1: hydrogen; 20% Pd/C / ethanol / 3 h
5.1: triphenylphosphine; azodicarboxylic acid bis(2-methoxyethyl) ester / toluene / 48 h / 0 °C / Molecular sieve
6.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 0 - 20 °C
With
azodicarboxylic acid bis(2-methoxyethyl) ester; 20% Pd/C; tetrabutyl ammonium fluoride; hydrogen; sodium methylate; triphenylphosphine;
In
tetrahydrofuran; methanol; ethanol; chloroform; 2,2,2-trifluoroethanol; water; toluene; acetonitrile;
5.1: |Mitsunobu Displacement;
DOI:10.1021/np300376f