Reaction equation
[CH3:1][C:2]1([CH3:21])[CH2:15][CH2:14][C:13]([CH3:17])([CH3:16])[C:12]2[CH:11]=[C:10]3[C:5]([CH:6]=[CH:7][C:8](B(O)O)=[CH:9]3)=[CH:4][C:3]1=2.[CH2:22]([N:25]1[CH:29]=[C:28](I)[CH:27]=[C:26]1[C:31]([O:33][CH3:34])=[O:32])[CH2:23][CH3:24]>>[CH2:22]([N:25]1[CH:29]=[C:28]([C:8]2[CH:7]=[CH:6][C:5]3[C:10](=[CH:11][C:12]4[C:13]([CH3:17])([CH3:16])[CH2:14][CH2:15][C:2]([CH3:21])([CH3:1])[C:3]=4[CH:4]=3)[CH:9]=2)[CH:27]=[C:26]1[C:31]([O:33][CH3:34])=[O:32])[CH2:23][CH3:24]Participants
3
Procedure
Following the basic procedure of Example 7(f), by reacting 1.7 g (6 mmol) of 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-anthrylboronic acid with 1.47 g (5 mmol) of methyl N-propyl-4-iodo-2-pyrrolecarboxylate, 450 mg (22%) of methyl N-propyl-4-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-anthryl)-2-pyrrolecarboxylate were obtained.
Sources & evidence
- ORD record
- ord-00a204d0f65b435cab8a71dca632e9c7
- Source dataset
- uspto-grants-1998_03
- Patent number
- US05723499
Linked notes
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