Technology Process of 23R,25-dihydroxyvitamin D3
There total 20 articles about 23R,25-dihydroxyvitamin D3 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:
-
C37H62O5Si;
With
toluene-4-sulfonic acid;
In
methanol;
at 20 ℃;
With
potassium carbonate;
In
methanol;
at 20 ℃;
DOI:10.1002/cbic.202100250
- Guidance literature:
-
C37H62O5Si;
With
toluene-4-sulfonic acid;
In
methanol;
at 20 ℃;
With
potassium carbonate;
In
methanol;
at 20 ℃;
DOI:10.1002/cbic.202100250
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: indium / tetrahydrofuran / 0 °C / Sonication
2.1: tetrahydrofuran / 0 °C
3.1: triethylamine; dmap / dichloromethane / Reflux
4.1: water; hydrogen fluoride / dichloromethane; acetonitrile / 20 °C
5.1: tetrapropylammonium perruthennate; 4-methylmorpholine N-oxide / dichloromethane / 20 °C / Molecular sieve
6.1: n-butyllithium / tetrahydrofuran / -78 °C
7.1: toluene-4-sulfonic acid / methanol / 20 °C
7.2: 20 °C
With
dmap; indium; n-butyllithium; tetrapropylammonium perruthennate; hydrogen fluoride; water; toluene-4-sulfonic acid; 4-methylmorpholine N-oxide; triethylamine;
In
tetrahydrofuran; methanol; dichloromethane; acetonitrile;
6.1: |Wittig Olefination;
DOI:10.1002/cbic.202100250