Technology Process of C33H40O4
There total 15 articles about C33H40O4 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:
-
Multi-step reaction with 10 steps
1: t-BuOK / tetrahydrofuran / 1 h / 0 °C
2: tetrahydrofuran / 1 h / -78 °C
3: TMSOTf / CH2Cl2 / 1 h / -78 °C
4: 70 percent / TiCl3(O-i-Pr) / CH2Cl2 / 1 h / -78 °C
5: lithium tri(t-butoxy)aluminum hydride / tetrahydrofuran / Ambient temperature
6: 2,6-lutidine / CH2Cl2 / 1 h / -23 °C
7: DIBAL / CH2Cl2; hexane / 1 h / -78 °C
8: diethylzinc / diethyl ether; hexane / 6 h / Ambient temperature
9: PDC, 4A molecular sieves / CH2Cl2 / 1.5 h / Ambient temperature
10: TBAF
With
2,6-dimethylpyridine; dipyridinium dichromate; titanium(IV) trichloride isopropoxide; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; potassium tert-butylate; tetrabutyl ammonium fluoride; diethylzinc; diisobutylaluminium hydride; lithium tri-t-butoxyaluminum hydride;
In
tetrahydrofuran; diethyl ether; hexane; dichloromethane;
DOI:10.1021/ja984250f
- Guidance literature:
-
Multi-step reaction with 12 steps
1: Ph3P / tetrahydrofuran / 0.17 h / -23 °C
2: tetrahydrofuran / 168 h / Ambient temperature
3: t-BuOK / tetrahydrofuran / 1 h / 0 °C
4: tetrahydrofuran / 1 h / -78 °C
5: TMSOTf / CH2Cl2 / 1 h / -78 °C
6: 70 percent / TiCl3(O-i-Pr) / CH2Cl2 / 1 h / -78 °C
7: lithium tri(t-butoxy)aluminum hydride / tetrahydrofuran / Ambient temperature
8: 2,6-lutidine / CH2Cl2 / 1 h / -23 °C
9: DIBAL / CH2Cl2; hexane / 1 h / -78 °C
10: diethylzinc / diethyl ether; hexane / 6 h / Ambient temperature
11: PDC, 4A molecular sieves / CH2Cl2 / 1.5 h / Ambient temperature
12: TBAF
With
2,6-dimethylpyridine; dipyridinium dichromate; titanium(IV) trichloride isopropoxide; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; potassium tert-butylate; tetrabutyl ammonium fluoride; diethylzinc; diisobutylaluminium hydride; lithium tri-t-butoxyaluminum hydride; triphenylphosphine;
In
tetrahydrofuran; diethyl ether; hexane; dichloromethane;
DOI:10.1021/ja984250f
- Guidance literature:
-
Multi-step reaction with 11 steps
1: tetrahydrofuran / 168 h / Ambient temperature
2: t-BuOK / tetrahydrofuran / 1 h / 0 °C
3: tetrahydrofuran / 1 h / -78 °C
4: TMSOTf / CH2Cl2 / 1 h / -78 °C
5: 70 percent / TiCl3(O-i-Pr) / CH2Cl2 / 1 h / -78 °C
6: lithium tri(t-butoxy)aluminum hydride / tetrahydrofuran / Ambient temperature
7: 2,6-lutidine / CH2Cl2 / 1 h / -23 °C
8: DIBAL / CH2Cl2; hexane / 1 h / -78 °C
9: diethylzinc / diethyl ether; hexane / 6 h / Ambient temperature
10: PDC, 4A molecular sieves / CH2Cl2 / 1.5 h / Ambient temperature
11: TBAF
With
2,6-dimethylpyridine; dipyridinium dichromate; titanium(IV) trichloride isopropoxide; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; potassium tert-butylate; tetrabutyl ammonium fluoride; diethylzinc; diisobutylaluminium hydride; lithium tri-t-butoxyaluminum hydride;
In
tetrahydrofuran; diethyl ether; hexane; dichloromethane;
DOI:10.1021/ja984250f