反応式
C[O:2][C:3]1[CH:8]=[CH:7][C:6](B(O)O)=[CH:5][CH:4]=1.[CH3:12][C:13]1([CH3:29])[CH2:18][C:17]([CH3:20])([CH3:19])[CH2:16][C:15](OS(C(F)(F)F)(=O)=O)=[CH:14]1>>[CH3:12][C:13]1([CH3:29])[CH2:18][C:17]([CH3:20])([CH3:19])[CH2:16][CH:15]([C:6]2[CH:7]=[CH:8][C:3]([OH:2])=[CH:4][CH:5]=2)[CH2:14]1参加物
3
実験手順
The title compound was prepared from 4-methoxy-benzeneboronic acid and trifluoro-methanesulfonic acid 3,3,5,5-tetramethyl-cyclohex-1-enyl ester in accordance with the procedure described in Step 1, Example 86.
出典と根拠
- ORDレコード
- ord-6977e0eeff3649f4a53ceae7dd33409a
- 出典データセット
- uspto-grants-2014_02
- 特許番号
- US08642603B2
関連ノート
読み込み中…