Dimethyl Sulfoxide → HCID 178445259, compound
Reaction equation
[CH3:36][CH2:37][N:38]([CH2:39][CH3:40])[CH2:41][CH3:42].[CH3:54][S:55](=[O:56])[CH3:57].[OH2:53].[S:49](=[O:50])(=[O:51])=[O:52].[c:1]1([C:7]([NH:8][CH:9]([CH2:10][CH:11]([CH3:12])[CH3:13])[C:14](=[O:15])[NH:16][CH:17]([CH2:18][CH2:19][CH2:20][CH3:21])[CH2:22][OH:23])([c:24]2[cH:25][cH:26][cH:27][cH:28][cH:29]2)[c:30]2[cH:31][cH:32][cH:33][cH:34][cH:35]2)[cH:2][cH:3][cH:4][cH:5][cH:6]1.[n:43]1[cH:44][cH:45][cH:46][cH:47][cH:48]1>>[c:1]1([C:7]([NH:8][CH:9]([CH2:10][CH:11]([CH3:12])[CH3:13])[C:14](=[O:15])[NH:16][CH:17]([CH2:18][CH2:19][CH2:20][CH3:21])[CH:22]=[O:23])([c:24]2[cH:25][cH:26][cH:27][cH:28][cH:29]2)[c:30]2[cH:31][cH:32][cH:33][cH:34][cH:35]2)[cH:2][cH:3][cH:4][cH:5][cH:6]1Participants
7
Sources & evidence
- ORD record
- ord-0898a25bd1b7426fa532a033642a5459
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (6/10)
Reaction notes
Loading…