Dimethyl Sulfoxide → HCID 57314607, compound
Reaction equation
[CH2:11]([CH3:12])[CH:13]1[C:14](=[O:76])[CH2:15][CH:16]([O:65][Si:66]([CH:67]([CH3:68])[CH3:69])([CH:70]([CH3:71])[CH3:72])[CH:73]([CH3:74])[CH3:75])[CH:17]([CH3:64])[CH:18]([C:52](=[CH:53][CH:54]2[CH2:55][CH:56]([O:61][CH3:62])[CH:57]([OH:60])[CH2:58][CH2:59]2)[CH3:63])[O:19][C:20](=[O:51])[CH:21]2[CH2:22][CH2:23][CH2:24][CH2:25][N:26]2[C:27](=[O:50])[C:28](=[O:49])[C:29]2([OH:48])[CH:30]([CH3:47])[CH2:31][CH:32]([O:45][CH3:46])[CH:33]([CH:34]([O:42][CH3:43])[CH2:35][CH:36]([CH3:41])[CH2:37][C:38]([CH3:40])=[CH:39]1)[O:44]2.[CH2:84]([Cl:85])[Cl:86].[CH3:77][CH2:78][N:79]([CH2:80][CH3:81])[CH2:82][CH3:83].[CH3:7][S:8](=[O:9])[CH3:10].[Cl:1][C:2]([C:3]([Cl:4])=[O:5])=[O:6].[OH2:87]>>[CH2:11]([CH3:12])[CH:13]1[C:14](=[O:76])[CH2:15][CH:16]([O:65][Si:66]([CH:67]([CH3:68])[CH3:69])([CH:70]([CH3:71])[CH3:72])[CH:73]([CH3:74])[CH3:75])[CH:17]([CH3:64])[CH:18]([C:52](=[CH:53][CH:54]2[CH2:55][CH:56]([O:61][CH3:62])[C:57](=[O:60])[CH2:58][CH2:59]2)[CH3:63])[O:19][C:20](=[O:51])[CH:21]2[CH2:22][CH2:23][CH2:24][CH2:25][N:26]2[C:27](=[O:50])[C:28](=[O:49])[C:29]2([OH:48])[CH:30]([CH3:47])[CH2:31][CH:32]([O:45][CH3:46])[CH:33]([CH:34]([O:42][CH3:43])[CH2:35][CH:36]([CH3:41])[CH2:37][C:38]([CH3:40])=[CH:39]1)[O:44]2Participants
7
Sources & evidence
- ORD record
- ord-46aaf489299546cdbec629dba434a078
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (5/10)
Reaction notes
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