Reaction equation
[C:1]([N:4]1[C:12]2[C:7](=[CH:8][C:9]([C:13](=[O:15])[CH3:14])=[CH:10][CH:11]=2)[CH2:6][C:5]1=[O:16])(=[O:3])[CH3:2].[C:17](O)(=[O:22])[CH2:18][CH:19]([CH3:21])[CH3:20]>>[C:1]([N:4]1[C:12]2[C:7](=[CH:8][C:9]([C:13](=[O:15])[CH3:14])=[CH:10][CH:11]=2)[C:6](=[C:17]([OH:22])[CH2:18][CH:19]([CH3:21])[CH3:20])[C:5]1=[O:16])(=[O:3])[CH3:2]Participants
3
Procedure
Prepared from 1,5-diacetyl-2-indolinone and isovaleric acid
Sources & evidence
- ORD record
- ord-a7dcbb6ffd164f4e996a4fa361d612a4
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07560480B2
Linked notes
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