Homoallyl bromide → 5-But-3-enyloxy-pyridine-2-carboxylic acid
Reaction equation
[Br:26][CH2:27][CH2:28][CH:29]=[CH2:30].[CH3:15][O:16][C:17]([c:18]1[cH:19][cH:20][c:21]([OH:22])[cH:23][n:24]1)=[O:25].[CH3:31][O:32][C:33]([c:34]1[cH:35][cH:36][c:37]([O:38][CH2:39][CH2:40][CH:41]=[CH2:42])[cH:43][n:44]1)=[O:45].[CH:1]1([CH2:4][O:5][c:6]2[cH:7][cH:8][c:9]([C:12](=[O:13])[OH:14])[n:10][cH:11]2)[CH2:2][CH2:3]1>>[CH2:1]([CH:2]=[CH2:3])[CH2:4][O:5][c:6]1[cH:7][cH:8][c:9]([C:12](=[O:13])[OH:14])[n:10][cH:11]1Participants
5
Sources & evidence
- ORD record
- ord-2039507d0d2c435f87653a010c0ec2ec
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (3/10)
Reaction notes
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