Technology Process of H2N-Lys(Z)-O-decyl(F17)
There total 3 articles about H2N-Lys(Z)-O-decyl(F17) which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
methoxybenzene; trifluoroacetic acid;
In
dichloromethane;
at 20 ℃;
for 15h;
DOI:10.1002/ejoc.201100648
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 20 °C / Inert atmosphere
1.2: 18 h / 20 °C / Inert atmosphere; Reflux
2.1: methoxybenzene; trifluoroacetic acid / dichloromethane / 15 h / 20 °C
With
benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; methoxybenzene; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid;
In
dichloromethane;
DOI:10.1002/ejoc.201100648
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 20 °C / Inert atmosphere
1.2: 18 h / 20 °C / Inert atmosphere; Reflux
2.1: methoxybenzene; trifluoroacetic acid / dichloromethane / 15 h / 20 °C
With
benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; methoxybenzene; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid;
In
dichloromethane;
DOI:10.1002/ejoc.201100648