Chloride → {5-[6-(cis-4-Butylcyclohexyloxy)-5-iodo-naphthalen-2-yl]-2,2-dimethyl-1,3-dioxinan-5-yl}-carbamic acid tert-butyl ester
Reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6]([NH:7][C:8]1([c:16]2[cH:17][c:18]3[cH:19][cH:20][c:21]([O:26][CH:27]4[CH2:28][CH2:29][CH:30]([CH2:33][CH2:34][CH2:35][CH3:36])[CH2:31][CH2:32]4)[cH:22][c:23]3[cH:24][cH:25]2)[CH2:9][O:10][C:11]([CH3:14])([CH3:15])[O:12][CH2:13]1)=[O:37].[CH2:46]([Cl:47])[Cl:48].[Cl-:49].[Cl-:50].[Cl-:51].[Cl-:52].[I:38][N:39]1[C:40](=[O:41])[CH2:42][CH2:43][C:44]1=[O:45].[Zr+4:53]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6]([NH:7][C:8]1([c:16]2[cH:17][c:18]3[cH:19][cH:20][c:21]([O:26][CH:27]4[CH2:28][CH2:29][CH:30]([CH2:33][CH2:34][CH2:35][CH3:36])[CH2:31][CH2:32]4)[c:22]([I:38])[c:23]3[cH:24][cH:25]2)[CH2:9][O:10][C:11]([CH3:14])([CH3:15])[O:12][CH2:13]1)=[O:37]Participants
6
Reactant 5
Product 1
Sources & evidence
- ORD record
- ord-3f37c5bd64b84e1999d20e22bec42457
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (5/10)
Reaction notes
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