3,5-Dichlorophenylboronic acid → HCID 178524507, compound
Reaction equation
[Br:1][c:2]1[cH:3][c:4]([CH2:5][N:6]([C:7](=[O:8])[c:9]2[c:10]([C:21](=[O:22])[OH:23])[cH:11][c:12]([C:18](=[O:19])[OH:20])[c:13]([C:15](=[O:16])[OH:17])[cH:14]2)[CH:24]2[CH2:25][CH2:26][CH2:27][c:28]3[cH:29][cH:30][cH:31][cH:32][c:33]32)[cH:34][cH:35][cH:36]1.[Cl:37][c:38]1[cH:39][c:40]([B:45]([OH:46])[OH:47])[cH:41][c:42]([Cl:44])[cH:43]1>>[c:2]1(-[c:40]2[cH:39][c:38]([Cl:37])[cH:43][c:42]([Cl:44])[cH:41]2)[cH:3][c:4]([CH2:5][N:6]([C:7](=[O:8])[c:9]2[c:10]([C:21](=[O:22])[OH:23])[cH:11][c:12]([C:18](=[O:19])[OH:20])[c:13]([C:15](=[O:16])[OH:17])[cH:14]2)[CH:24]2[CH2:25][CH2:26][CH2:27][c:28]3[cH:29][cH:30][cH:31][cH:32][c:33]32)[cH:34][cH:35][cH:36]1Participants
3
Sources & evidence
- ORD record
- ord-db9c09aa40b84bdf9566273f4d38f378
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (7/10)
Reaction notes
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