5-Hexen-1-ol → N-[(Hex-5-en-1-yloxy)carbonyl]-L-norleucine
Reaction equation
[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)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][CH:5]=[CH2:18]Participants
3
Procedure
N-[(Hex-5-en-1-yloxy)carbonyl]-L-norleucine was prepared according to the procedure for N-[(pent-4-en-1-yloxy)carbonyl]-L-norleucine by using 5-hexenol instead of 4-pentenol. LRMS (ESI) m/z 258 [(M+H)+; calcd for C13H24NO4: 258].
Sources & evidence
- ORD record
- ord-acabccb6db764d8cb92b8063355c7b52
- Source dataset
- uspto-grants-2012_07
- Patent number
- US08216999B2
Reaction notes
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