N-Hydroxyphthalimide → Tert-butyl 4-(1,3-dioxoisoindolin-2-yloxy)piperidine-1-carboxylate
Reaction equation
[N:46]([C:47]([O:48][CH:49]([CH3:50])[CH3:51])=[O:52])=[N:53][C:54]([O:55][CH:56]([CH3:57])[CH3:58])=[O:59].[OH:1][CH:2]1[CH2:3][CH2:4][N:5]([C:8](=[O:9])[O:10][C:11]([CH3:12])([CH3:13])[CH3:14])[CH2:6][CH2:7]1.[OH:34][N:35]1[C:36](=[O:45])[c:37]2[cH:38][cH:39][cH:40][cH:41][c:42]2[C:43]1=[O:44].[c:15]1([P:16]([c:17]2[cH:18][cH:19][cH:20][cH:21][cH:22]2)[c:23]2[cH:24][cH:25][cH:26][cH:27][cH:28]2)[cH:29][cH:30][cH:31][cH:32][cH:33]1>>[O:1]([CH:2]1[CH2:3][CH2:4][N:5]([C:8](=[O:9])[O:10][C:11]([CH3:12])([CH3:13])[CH3:14])[CH2:6][CH2:7]1)[N:35]1[C:36](=[O:45])[c:37]2[cH:38][cH:39][cH:40][cH:41][c:42]2[C:43]1=[O:44]Participants
5
Sources & evidence
- ORD record
- ord-4591314ba47a4a378c9251df7a68c55d
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (5/10)
Reaction notes
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