Hydroxylamine → HCID 178447787, compound
Reaction equation
[CH2:51]1[O:52][CH2:53][CH2:54][CH2:55]1.[CH3:1][S:2](=[O:3])(=[O:4])[N:5]1[CH2:6][CH2:7][N:8]([c:11]2[cH:12][cH:13][c:14]([C:17]#[C:18][Si:19]([CH3:20])([CH3:21])[CH3:22])[cH:15][cH:16]2)[CH2:9][CH2:10]1.[CH3:24][Si:25]([N-:26][Si:27]([CH3:28])([CH3:29])[CH3:30])([CH3:31])[CH3:32].[Cl:33][Si:34]([CH3:35])([CH3:36])[CH3:37].[Li+:23].[NH2:49][OH:50].[c:38]1([CH:44]([CH2:45][CH:46]=[O:47])[CH3:48])[cH:39][cH:40][cH:41][cH:42][cH:43]1>>[CH2:1]([S:2](=[O:3])(=[O:4])[N:5]1[CH2:6][CH2:7][N:8]([c:11]2[cH:12][cH:13][c:14]([C:17]#[C:18][Si:19]([CH3:20])([CH3:21])[CH3:22])[cH:15][cH:16]2)[CH2:9][CH2:10]1)[CH:46]([CH2:45][CH:44]([c:38]1[cH:39][cH:40][cH:41][cH:42][cH:43]1)[CH3:48])[NH:49][OH:50]Participants
8
Sources & evidence
- ORD record
- ord-e6c7ea8f953c4e388f8869947eced88d
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (7/10)
Reaction notes
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