4-Aminocarbonylphenylboronic acid → HCID 57488973, compound
Reaction equation
[Cl:1][c:2]1[c:3]([Cl:40])[cH:4][c:5]2[c:6]([cH:39]1)[N:7]([CH2:12][C:13](=[O:14])[N:15]([CH:16]([CH2:17][N:18]1[CH2:19][CH2:20][CH2:21][CH2:22]1)[c:23]1[cH:24][cH:25][c:26](-[c:29]3[cH:30][cH:31][cH:32][c:33]([C:34]([NH2:35])=[O:36])[cH:37]3)[cH:27][cH:28]1)[CH3:38])[C:8](=[O:11])[CH2:9][O:10]2.[NH2:41][C:42](=[O:43])[c:44]1[cH:45][cH:46][c:47]([B:50]([OH:51])[OH:52])[cH:48][cH:49]1>>[Cl:1][c:2]1[c:3]([Cl:40])[cH:4][c:5]2[c:6]([cH:39]1)[N:7]([CH2:12][C:13](=[O:14])[N:15]([CH:16]([CH2:17][N:18]1[CH2:19][CH2:20][CH2:21][CH2:22]1)[c:23]1[cH:24][cH:25][c:26](-[c:47]3[cH:46][cH:45][c:44]([C:42]([NH2:41])=[O:43])[cH:49][cH:48]3)[cH:27][cH:28]1)[CH3:38])[C:8](=[O:11])[CH2:9][O:10]2Participants
3
Sources & evidence
- ORD record
- ord-30a9477e3e4c4b38959a240d263fa910
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (8/10)
Reaction notes
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