Chloride → 1-Cyclohexylbut-3-yn-2-ol
Reaction equation
[CH3:1][Si:2]([C:3]#[C:4][Si:5]([CH3:6])([CH3:7])[CH3:8])([CH3:9])[CH3:10].[CH:12]1([CH2:13][C:14]([OH:15])=[O:16])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21]1.[CH:45]1([CH2:51][C:52]([C:53]#[CH:54])=[O:55])[CH2:46][CH2:47][CH2:48][CH2:49][CH2:50]1.[Cl-:11].[Na+:22].[Na+:23].[OH2:24].[OH2:25].[OH2:26].[OH2:27].[OH2:28].[OH2:29].[OH2:30].[OH2:31].[OH:32][B:33]1[O:34][B-:35]2([OH:44])[O:36][B-:37]([OH:42])([O:38][B:39]([OH:41])[O:40]2)[O:43]1>>[CH:45]1([CH2:51][CH:52]([C:53]#[CH:54])[OH:55])[CH2:46][CH2:47][CH2:48][CH2:49][CH2:50]1Participants
8
Sources & evidence
- ORD record
- ord-75b4aa36c0744f20853819856ce42beb
- Source dataset
- Test data from https://doi.org/10.1039/C8SC04228D
Reaction notes
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