Phenylboronic Acid → HCID 21462922, compound
Reaction equation
[Br:1][c:2]1[cH:3][cH:4][c:5]2[c:6]([cH:7]1)[c:8]1[n:9]([CH2:29][c:30]3[c:31]([O:38][CH3:39])[cH:32][cH:33][c:34]([O:36][CH3:37])[cH:35]3)[c:10](=[O:28])[c:11]([C:23](=[O:24])[O:25][CH2:26][CH3:27])[c:12](-[c:15]3[cH:16][cH:17][c:18]([O:21][CH3:22])[cH:19][cH:20]3)[c:13]1[o:14]2.[OH:40][B:41]([OH:42])[c:43]1[cH:44][cH:45][cH:46][cH:47][cH:48]1>>[c:2]1(-[c:43]2[cH:44][cH:45][cH:46][cH:47][cH:48]2)[cH:3][cH:4][c:5]2[c:6]([cH:7]1)[c:8]1[n:9]([CH2:29][c:30]3[c:31]([O:38][CH3:39])[cH:32][cH:33][c:34]([O:36][CH3:37])[cH:35]3)[c:10](=[O:28])[c:11]([C:23](=[O:24])[O:25][CH2:26][CH3:27])[c:12](-[c:15]3[cH:16][cH:17][c:18]([O:21][CH3:22])[cH:19][cH:20]3)[c:13]1[o:14]2Participants
3
Sources & evidence
- ORD record
- ord-e813d7165ab0422eaed2206bf7eff8a5
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (10/10)
Reaction notes
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