Reaction equation
[C:1]1([B:7]([CH:9]([O:16][CH:17]([B:24]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[OH:25])[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[OH:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:32]([NH:36][CH2:37][CH2:38]O)[CH2:33][CH2:34][CH3:35]>C(O)C>[C:1]1([B:7]([CH:9]([O:16][CH:17]([B:24]([C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=2)[O:25][CH2:38][CH2:37][NH:36][CH2:32][CH2:33][CH2:34][CH3:35])[C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[O:8][CH2:38][CH2:37][NH:36][CH2:32][CH2:33][CH2:34][CH3:35])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The entitled compound (35 mg) was obtained by allowing 40.6 mg of bis(4,4′-(phenylhydroxyboryl)benzyl) ether and 23 mg of N-n-butylethanolamine to act in 1 mL of ethanol.
Sources & evidence
- ORD record
- ord-53d81728ad064952a5975bf43eaa37ba
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08017809B2
Linked notes
Loading…