Ammonium → tert-Butyl 5-ethenyl-1H-indole-1-carboxylate
Reaction equation
[Br-:26].[C:6]([CH3:7])([CH3:8])([CH3:9])[O:10][C:11](=[O:12])[n:13]1[cH:14][cH:15][c:16]2[cH:17][c:18]([CH:22]=[O:23])[cH:19][cH:20][c:21]12.[CH2:47]1[O:48][CH2:49][CH2:50][CH2:51]1.[CH3:1][CH2:2][CH2:3][CH2:4][Li:5].[CH3:27][P+:28]([c:29]1[cH:30][cH:31][cH:32][cH:33][cH:34]1)([c:35]1[cH:36][cH:37][cH:38][cH:39][cH:40]1)[c:41]1[cH:42][cH:43][cH:44][cH:45][cH:46]1.[Cl-:24].[NH4+:25]>>[CH2:1]=[CH:22][c:18]1[cH:17][c:16]2[cH:15][cH:14][n:13]([C:11]([O:10][C:6]([CH3:7])([CH3:8])[CH3:9])=[O:12])[c:21]2[cH:20][cH:19]1Participants
8
Sources & evidence
- ORD record
- ord-0515606ff2374b8bbc088ae8a5ce3aa2
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (1/10)
Reaction notes
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