Benzenesulfonyl chloride → HCID 68997020, compound
Reaction equation
[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[O:8][c:9]1[c:10]([N:22]2[CH2:23][C:24](=[O:35])[N:25]([CH2:29][CH2:30][Si:31]([CH3:32])([CH3:33])[CH3:34])[S:26]2(=[O:27])=[O:28])[cH:11][cH:12][c:13]([CH:15]=[CH:16][CH:17]2[CH2:18][NH:19][CH2:20][CH2:21]2)[cH:14]1.[c:36]1([S:42](=[O:43])(=[O:44])[Cl:45])[cH:37][cH:38][cH:39][cH:40][cH:41]1>>[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[O:8][c:9]1[c:10]([N:22]2[CH2:23][C:24](=[O:35])[N:25]([CH2:29][CH2:30][Si:31]([CH3:32])([CH3:33])[CH3:34])[S:26]2(=[O:27])=[O:28])[cH:11][cH:12][c:13]([CH:15]=[CH:16][CH:17]2[CH2:18][N:19]([S:42]([c:36]3[cH:37][cH:38][cH:39][cH:40][cH:41]3)(=[O:43])=[O:44])[CH2:20][CH2:21]2)[cH:14]1Participants
3
Sources & evidence
- ORD record
- ord-1d48d8c05dc24fafadd58ce267131594
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (9/10)
Reaction notes
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