Citric Acid → (1H-indol-2-yl)methanol
Reaction equation
[CH2:22]([N:23]=[C:24]=[N:25][CH2:26][CH2:27][CH2:28][N:29]([CH3:30])[CH3:31])[CH3:32].[CH3:51][N:52]([CH3:53])[CH:54]=[O:55].[ClH:21].[O:46]1[CH2:47][CH2:48][CH2:49][CH2:50]1.[OH:13][N:14]1[C:15](=[O:16])[CH2:17][CH2:18][C:19]1=[O:20].[OH:33][C:34]([CH2:35][C:36]([C:37](=[O:38])[OH:39])([CH2:40][C:41](=[O:42])[OH:43])[OH:44])=[O:45].[nH:1]1[c:2]([C:10](=[O:11])[OH:12])[cH:3][c:4]2[cH:5][cH:6][cH:7][cH:8][c:9]12>>[nH:1]1[c:2]([CH2:10][OH:11])[cH:3][c:4]2[cH:5][cH:6][cH:7][cH:8][c:9]12Participants
8
Sources & evidence
- ORD record
- ord-5736af391eb64739a54b45fbe5fa4a7c
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (10/10)
Reaction notes
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