反応式
[C:1]1([C:7]#[C:8][C:9]#[C:10][C:11]#[C:12][C@@H:13]2[O:15][C@H:14]2[CH:16]=[CH:17][CH2:18][OH:19])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C([O:24]O)(C)(C)C>C1C=CC=CC=1.C/C(/O)=C\C(C)=O.C/C(/O)=C\C(C)=O.O=[V]>[C:1]1([C:7]#[C:8][C:9]#[C:10][C:11]#[C:12][CH:13]2[O:15][CH:14]2[C@@H:16]2[O:24][C@H:17]2[CH2:18][OH:19])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1参加物
5
実験手順
To a stirred solution of 22 mg (0.089 mmole) of (trans)-3-[3-(6-phenyl-1,3,5-hexatriynyl)oxiranyl]-2-propen-1-ol (see example 6) in 5 ml of dry benzene was added 2 mg of vanadyl acetylacetonate and 50 μl (0.26 mmole) of a 5.43M solution of t-butylhydroperoxide in benzene. The mixture was stirred for 4 hours. The mixture was concentrated and the residue was purified via preparative thin layer chromatography (silica gel; ethyl acetate-hexane 1:1) to afford 11 mg of the title compound as an approximately 1:1 mixture of diastereomers.
後処理
- concentrationThe mixture was concentrated
- customthe residue was purified via preparative thin layer chromatography (silica gel; ethyl acetate-hexane 1:1)
出典と根拠
- ORDレコード
- ord-054629668bf84860bef5a8229ea8ea7d
- 出典データセット
- uspto-grants-1987_03
- 特許番号
- US04654426
関連ノート
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