Technology Process of Butanoic acid, (3-oxo-2-phenyl-5-isoxazolidinyl)methyl ester, (R)-
There total 6 articles about Butanoic acid, (3-oxo-2-phenyl-5-isoxazolidinyl)methyl ester, (R)- 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 5 steps
1: diethyl ether / 0.25 h
2: 48 percent / aq. sodium bicarbonate / diethyl ether / Ambient temperature
3: 61 percent / NaBH4, LiCl / tetrahydrofuran; methanol / 0.17 h
4: pyridine / CH2Cl2
5: potassium phosphate buffer, pH 7 / lipase PS / acetone / Ambient temperature
With
pyridine; sodium tetrahydroborate; potassium phosphate buffer; sodium hydrogencarbonate; lithium chloride;
Lipase PS;
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane; acetone;
DOI:10.1021/jo00036a013
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 61 percent / NaBH4, LiCl / tetrahydrofuran; methanol / 0.17 h
2: pyridine / CH2Cl2
3: potassium phosphate buffer, pH 7 / lipase PS / acetone / Ambient temperature
With
pyridine; sodium tetrahydroborate; potassium phosphate buffer; lithium chloride;
Lipase PS;
In
tetrahydrofuran; methanol; dichloromethane; acetone;
DOI:10.1021/jo00036a013
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 48 percent / aq. sodium bicarbonate / diethyl ether / Ambient temperature
2: 61 percent / NaBH4, LiCl / tetrahydrofuran; methanol / 0.17 h
3: pyridine / CH2Cl2
4: potassium phosphate buffer, pH 7 / lipase PS / acetone / Ambient temperature
With
pyridine; sodium tetrahydroborate; potassium phosphate buffer; sodium hydrogencarbonate; lithium chloride;
Lipase PS;
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane; acetone;
DOI:10.1021/jo00036a013