Trifluoromethanesulfonic acid → HCID 178436250, compound
Reaction equation
[CH2:1]([CH3:2])[CH:3]1[C:4](=[O:63])[CH2:5][CH:6]([O:55][Si:56]([CH3:57])([CH3:58])[C:59]([CH3:60])([CH3:61])[CH3:62])[CH:7]([CH3:54])[CH:8]([C:42](=[CH:43][CH:44]2[CH2:45][CH:46]([O:51][CH3:52])[CH:47]([OH:50])[CH2:48][CH2:49]2)[CH3:53])[O:9][C:10](=[O:41])[CH:11]2[CH2:12][CH2:13][CH2:14][CH2:15][N:16]2[C:17](=[O:40])[C:18](=[O:39])[C:19]2([OH:38])[CH:20]([CH3:37])[CH2:21][CH:22]([O:35][CH3:36])[CH:23]([CH:24]([O:32][CH3:33])[CH2:25][CH:26]([CH3:31])[CH2:27][C:28]([CH3:30])=[CH:29]1)[O:34]2.[Cl:64][C:65]([Cl:66])([Cl:67])[C:84](=[NH:85])[O:86][CH2:68][c:69]1[cH:70][c:71]([CH:75]([O:76][SiH:77]([CH3:78])[CH3:79])[C:80]([CH3:81])([CH3:82])[CH3:83])[cH:72][cH:73][cH:74]1.[OH:87][S:88]([C:89]([F:90])([F:91])[F:92])(=[O:93])=[O:94]>>[CH2:1]([CH3:2])[CH:3]1[C:4](=[O:63])[CH2:5][CH:6]([O:55][Si:56]([CH3:57])([CH3:58])[C:59]([CH3:60])([CH3:61])[CH3:62])[CH:7]([CH3:54])[CH:8]([C:42](=[CH:43][CH:44]2[CH2:45][CH:46]([O:51][CH3:52])[CH:47]([O:50][CH2:68][c:69]3[cH:70][c:71]([CH:75]([O:76][SiH:77]([CH3:78])[CH3:79])[C:80]([CH3:81])([CH3:82])[CH3:83])[cH:72][cH:73][cH:74]3)[CH2:48][CH2:49]2)[CH3:53])[O:9][C:10](=[O:41])[CH:11]2[CH2:12][CH2:13][CH2:14][CH2:15][N:16]2[C:17](=[O:40])[C:18](=[O:39])[C:19]2([OH:38])[CH:20]([CH3:37])[CH2:21][CH:22]([O:35][CH3:36])[CH:23]([CH:24]([O:32][CH3:33])[CH2:25][CH:26]([CH3:31])[CH2:27][C:28]([CH3:30])=[CH:29]1)[O:34]2Participants
4
Reactant 3
HCID 62406Trifluoromethanesulfonic acid
HCID 5724677817-Ethyl-1-hydroxy-12-[2'-(4"-hydroxy-3"-methoxycyclohexyl)-1'-methylvinyl]-14-t-butyl-dimethylsilyloxy-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9]octacos-18-ene-2,3,10,16-tetraone
HCID 178504469HCID 178504469, compoundProduct 1
Sources & evidence
- ORD record
- ord-87f1811c35d74134bdfb9ee63f6c49ad
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (4/10)
Reaction notes
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