反応式
[NH2:1][C@H:2]([C:11]([OH:13])=[O:12])[CH2:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][CH:5]=1.CO.O>C(#N)C>[NH2:1][C@@H:2]([C:11]([OH:13])=[O:12])[CH2:3][C:4]1[CH:5]=[CH:6][C:7]([OH:10])=[CH:8][CH:9]=1参加物
5
実験手順
Example 1 was repeated with the difference that the sample to be tested was a tyrosine of unknown enantiomer composition, the comparison samples were (RS)-, (R)-, and (S)-tyrosine, and the mobile phase was a mixture of methanol, water, and acetonitrile in a 1:1:0.6 ratio by volume. In this case, the (R)-tyrosine gave a spot with an Rf -value of 0.34 and the (S)-tyrosine gave a spot with an Rf value of 0.26.
出典と根拠
- ORDレコード
- ord-b797c9bf619347f691fe461e33ed48fa
- 出典データセット
- uspto-grants-1986_05
- 特許番号
- US04590167
関連ノート
読み込み中…