Dimethyl Sulfoxide → HCID 57251512, compound
Reaction equation
[CH2:11]([CH3:12])[CH:13]1[C:14](=[O:78])[CH2:15][CH:16]([O:67][Si:68]([CH:69]([CH3:70])[CH3:71])([CH:72]([CH3:73])[CH3:74])[CH:75]([CH3:76])[CH3:77])[CH:17]([CH3:66])[CH:18]([C:52](=[CH:53][CH:54]2[CH2:55][CH:56]([O:61][CH2:62][CH:63]=[CH2:64])[CH:57]([OH:60])[CH2:58][CH2:59]2)[CH3:65])[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.[CH2:86]([Cl:87])[Cl:88].[CH3:79][CH2:80][N:81]([CH2:82][CH3:83])[CH2:84][CH3:85].[CH3:7][S:8](=[O:9])[CH3:10].[Cl:1][C:2]([C:3]([Cl:4])=[O:5])=[O:6].[OH2:89]>>[CH2:11]([CH3:12])[CH:13]1[C:14](=[O:78])[CH2:15][CH:16]([O:67][Si:68]([CH:69]([CH3:70])[CH3:71])([CH:72]([CH3:73])[CH3:74])[CH:75]([CH3:76])[CH3:77])[CH:17]([CH3:66])[CH:18]([C:52](=[CH:53][CH:54]2[CH2:55][CH:56]([O:61][CH2:62][CH:63]=[CH2:64])[C:57](=[O:60])[CH2:58][CH2:59]2)[CH3:65])[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-1d8ae575f0e143edaaa33fb91ca050e8
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (3/10)
Reaction notes
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