Technology Process of C27H43N3O6
There total 10 articles about C27H43N3O6 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:
-
Boc-Leu-Phe-MeLeu-OMe;
With
dihydrogen peroxide; lithium hydroxide;
In
methanol;
at 0 ℃;
With
hydrogenchloride; sodium thiosulfate;
In
methanol; water;
pH=1;
DOI:10.1016/j.tet.2011.11.089
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 20 °C / Inert atmosphere
2.1: dihydrogen peroxide; lithium hydroxide / methanol / 0 °C
2.2: pH 1
3.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 20 °C / Inert atmosphere
4.1: dihydrogen peroxide; lithium hydroxide / methanol / 0 °C
4.2: pH 1
With
dihydrogen peroxide; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; lithium hydroxide;
In
methanol; dichloromethane;
DOI:10.1016/j.tet.2011.11.089
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: methoxybenzene; trifluoroacetic acid / dichloromethane / 0.67 h
2.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / dichloromethane / 1.5 h / 20 °C / Inert atmosphere
3.1: dihydrogen peroxide; lithium hydroxide / methanol / 0 °C
3.2: pH 1
With
dihydrogen peroxide; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; methoxybenzene; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; lithium hydroxide;
In
methanol; dichloromethane;
DOI:10.1016/j.tet.2011.11.089