Hept-6-en-1-ol → N-[(Hept-6-en-1-yloxy)carbonyl]-L-norleucine
Reaktionsgleichung
[CH2:1]([O:6][C:7]([NH:9][C@H:10]([C:15]([OH:17])=[O:16])[CH2:11][CH2:12][CH2:13][CH3:14])=[O:8])[CH2:2][CH2:3][CH:4]=[CH2:5].[CH2:18](O)[CH2:19]CCCC=C>>[CH2:1]([O:6][C:7]([NH:9][C@H:10]([C:15]([OH:17])=[O:16])[CH2:11][CH2:12][CH2:13][CH3:14])=[O:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH:18]=[CH2:19]Komponenten
3
Versuchsvorschrift
N-[(Hept-6-en-1-yloxy)carbonyl]-L-norleucine was prepared according to the procedure for N-[(pent-4-en-1-yloxy)carbonyl]-L-norleucine by using 6-heptenol instead of 4-pentenol. LRMS (ESI) m/z 272 [(M+H)+; calcd for C14H26NO4: 272].
Quellen und Nachweise
- ORD-Eintrag
- ord-7250f4100c214379a286b20366403340
- Quelldatensatz
- uspto-grants-2012_07
- Patentnummer
- US08216999B2
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