Technology Process of Ser(Bzl)-Tyr(Bzl)-Gly-Leu-OBzl
There total 5 articles about Ser(Bzl)-Tyr(Bzl)-Gly-Leu-OBzl 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
trifluoroacetic acid;
In
dichloromethane;
for 0.25h;
Ambient temperature;
DOI:10.1021/jm00138a009
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 76 percent / 1-hydroxybenzotriazole (HBT), dicyclohexylcarbodiimide (DCC) / CH2Cl2 / 16 h / 0 °C
2: 50percent F3AcOH / CH2Cl2 / 0.25 h / Ambient temperature
With
benzotriazol-1-ol; dicyclohexyl-carbodiimide; trifluoroacetic acid;
In
dichloromethane;
DOI:10.1021/jm00138a009
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 4 M HCl / ethyl acetate / 0.33 h
2: 91 percent / TEA, dicycloxexylcarbodiimide (DCC), 1-hydroxybenzotriazole (HBT) / CH2Cl2 / 16 h / 0 °C
3: 4 N KOH / methanol / 0.83 h / 0 °C
4: 76 percent / 1-hydroxybenzotriazole (HBT), dicyclohexylcarbodiimide (DCC) / CH2Cl2 / 16 h / 0 °C
5: 50percent F3AcOH / CH2Cl2 / 0.25 h / Ambient temperature
With
hydrogenchloride; potassium hydroxide; TEA; benzotriazol-1-ol; dicyclohexyl-carbodiimide; trifluoroacetic acid;
In
methanol; dichloromethane; ethyl acetate;
DOI:10.1021/jm00138a009
