Hydrogen Bromide → 2-(1-(4-Bromophenyl)-3-(1,3-dioxan-2-yl)-1-oxopropan-2-yl) 1-tert-butyl pyrrolidine-1,2-dicarboxylate
Reaction equation
[Br:1].[Br:2][c:3]1[cH:4][cH:5][c:6]([C:9]([CH2:10][CH2:11][CH:12]2[O:13][CH2:14][CH2:15][CH2:16][O:17]2)=[O:18])[cH:7][cH:8]1.[C:19](=[O:20])([O:21][C:22]([CH3:23])([CH3:24])[CH3:25])[N:26]1[CH:27]([C:28](=[O:29])[OH:30])[CH2:31][CH2:32][CH2:33]1.[CH2:48]1[O:49][CH2:50][CH2:51][O:52][CH2:53]1.[CH3:43][CH2:44][O:45][CH2:46][CH3:47].[CH:34]([N:35]([CH2:36][CH3:37])[CH:38]([CH3:39])[CH3:40])([CH3:41])[CH3:42]>>[Br:2][c:3]1[cH:4][cH:5][c:6]([C:9]([CH:10]([CH2:11][CH:12]2[O:13][CH2:14][CH2:15][CH2:16][O:17]2)[O:30][C:28]([CH:27]2[N:26]([C:19](=[O:20])[O:21][C:22]([CH3:23])([CH3:24])[CH3:25])[CH2:33][CH2:32][CH2:31]2)=[O:29])=[O:18])[cH:7][cH:8]1Participants
7
Reactant 6
Product 1
Sources & evidence
- ORD record
- ord-2b4132d273094307a51a8867e9d40edc
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (4/10)
Reaction notes
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