Technology Process of (7R,7′S,8R,8′S)-4,4′-dibenzyloxy-3,3′-dimethoxy-7,7′-epoxylignane-9,9′-diol
There total 3 articles about (7R,7′S,8R,8′S)-4,4′-dibenzyloxy-3,3′-dimethoxy-7,7′-epoxylignane-9,9′-diol 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:
-
C36H40O11S2;
With
1,8-diazabicyclo[5.4.0]undec-7-ene; sodium iodide;
In
N,N-dimethyl-formamide;
at 80 ℃;
for 0.5h;
With
boron trichloride methyl sulfide complex;
In
tetrahydrofuran; N,N-dimethyl-formamide;
at 20 ℃;
for 1h;
With
dihydrogen peroxide; sodium hydrogencarbonate;
In
tetrahydrofuran; water; N,N-dimethyl-formamide;
DOI:10.1021/jf4046396
- Guidance literature:
-
C34H32O5;
With
dimethylsulfide borane complex;
In
tetrahydrofuran;
at 20 ℃;
for 1h;
With
water; dihydrogen peroxide; sodium hydrogencarbonate;
In
tetrahydrofuran;
DOI:10.1021/jf4046396
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: triethylamine / dichloromethane / 0.5 h / 20 °C
2.1: sodium iodide; 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 0.5 h / 80 °C
2.2: 1 h / 20 °C
With
1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; sodium iodide;
In
dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jf4046396