反応式
[CH3:1][C:2]1[CH2:7][CH2:6][CH2:5][C:4]([CH3:9])([CH3:8])[C:3]=1/[CH:10]=[CH:11]/[C:12](/[CH3:22])=[CH:13]/[CH:14]([CH2:16]/[C:17](/[CH3:21])=[CH:18]\[CH2:19][OH:20])C.[BH4-].[Na+].CC1CCCC(C)(C)C=1/C=C/C(/C)=C\C=C\C(\C)=C\C=O>>[CH3:1][C:2]1[CH2:7][CH2:6][CH2:5][C:4]([CH3:8])([CH3:9])[C:3]=1/[CH:10]=[CH:11]/[C:12](/[CH3:22])=[CH:13]\[CH:14]=[CH:16]\[C:17](\[CH3:21])=[CH:18]\[CH2:19][OH:20]参加物
4
実験手順
All-trans-retinol was obtained as a gift from Dr. Christian Eckhoff of Hoffmann-LaRoche, Inc. (Nutley, N.J.), and 13-cis-retinol was purchased from Sigma. 9-cis-Retinol was synthesized by NaBH4 reduction of authentic 9-cis-retinaldehyde (Sigma) and subsequently purified by normal phase HPLC essentially as we have described for 11-cis-retinol synthesis and purification (25). All-trans-, 13-cis-, and 9-cis-retinaldehydes were purchased from Sigma.
後処理
- customsubsequently purified by normal phase HPLC essentially as we
- customhave described for 11-cis-retinol synthesis and purification (25)
出典と根拠
- ORDレコード
- ord-fed8c9324be34a5a8e6c9e26c2754501
- 出典データセット
- uspto-grants-2007_03
- 特許番号
- US07186534B1
関連ノート
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