Chloride → 1,3-Di(tert-butyloxycarbonylamino)-2-(p-toluenesulfonyloxy)propane
Reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[NH:8][CH2:9][CH:10]([CH2:11][NH:12][C:13](=[O:14])[O:15][C:16]([CH3:17])([CH3:18])[CH3:19])[OH:20].[CH3:21][CH2:22][N:23]([CH2:24][CH3:25])[CH2:26][CH3:27].[Cl-:39].[Cl:40][CH2:41][Cl:42].[OH2:43].[S:28](=[O:29])(=[O:30])([c:31]1[cH:32][cH:33][c:34]([CH3:35])[cH:36][cH:37]1)[Cl:38]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[NH:8][CH2:9][CH:10]([CH2:11][NH:12][C:13](=[O:14])[O:15][C:16]([CH3:17])([CH3:18])[CH3:19])[O:20][S:28](=[O:29])(=[O:30])[c:31]1[cH:32][cH:33][c:34]([CH3:35])[cH:36][cH:37]1Participants
7
Sources & evidence
- ORD record
- ord-4ff89cc53ad54ad6b18b98105f273c42
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (7/10)
Reaction notes
Loading…