Oxalic Acid → HCID 178510641, compound
Reaction equation
[C:1](#[N:2])[C:3]1([NH:6][C:7](=[O:8])[CH:9]2[CH:10]([C:28](=[O:29])[N:30]3[CH2:31][C:32]([F:34])([F:35])[CH2:33]3)[CH2:11][CH:12]([S:14](=[O:15])(=[O:16])[c:17]3[c:18]([C:24]([F:25])([F:26])[F:27])[cH:19][c:20]([F:23])[cH:21][cH:22]3)[CH2:13]2)[CH2:4][CH2:5]1.[CH2:36]1[O:37][CH2:38][C:39]12[CH2:40][NH:41][CH2:42]2.[OH:43][C:44]([C:45](=[O:46])[OH:47])=[O:48]>>[C:1](#[N:2])[C:3]1([NH:6][C:7](=[O:8])[CH:9]2[CH:10]([C:28](=[O:29])[N:30]3[CH2:31][C:32]([F:34])([F:35])[CH2:33]3)[CH2:11][CH:12]([S:14](=[O:15])(=[O:16])[c:17]3[c:18]([C:24]([F:25])([F:26])[F:27])[cH:19][c:20]([N:41]4[CH2:40][C:39]5([CH2:36][O:37][CH2:38]5)[CH2:42]4)[cH:21][cH:22]3)[CH2:13]2)[CH2:4][CH2:5]1Participants
4
Sources & evidence
- ORD record
- ord-90b96d75af6d4a779c912429403c3db2
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (10/10)
Reaction notes
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