Reaktionsgleichung
CC(C)(C)[C@@H](C(O)=O)N[C:5](OCCCC=C)=[O:6].[NH2:18][C@@H:19]([CH:23]1[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]1)[C:20]([OH:22])=[O:21].[CH3:29][C:30]([CH3:37])([CH2:33][CH2:34][CH:35]=[CH2:36])[CH2:31][OH:32]>>[CH:23]1([C@H:19]([NH:18][C:5]([O:32][CH2:31][C:30]([CH3:37])([CH3:29])[CH2:33][CH2:34][CH:35]=[CH2:36])=[O:6])[C:20]([OH:22])=[O:21])[CH2:28][CH2:27][CH2:26][CH2:25][CH2:24]1Komponenten
4
Versuchsvorschrift
(2S)-Cyclohexyl({[(2,2-dimethylhex-5-en-1-yl)oxy]carbonyl}amino)acetic acid was prepared according to the procedure for 3-methyl-N-[(pent-4-enyloxy)carbonyl]-L-valine using (2S)-amino(cyclohexyl)acetic acid and 2,2-dimethylhex-5-en-1-ol. LRMS (ESI) m/z 312.3 [(M+H)+; calcd for C17H30NO4: 312.2].
Quellen und Nachweise
- ORD-Eintrag
- ord-3beae7aac3094a5e874349abe5fceef8
- Quelldatensatz
- uspto-grants-2012_07
- Patentnummer
- US08216999B2
Verknüpfte Notizen
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