反応式
[CH3:1][C:2]([O:4][CH2:5][C@H:6]1[O:11][C@@H:10]([O:12]C(C)=O)[C@H:9]([O:16][C:17]([CH3:19])=[O:18])[C@@H:8]([O:20][C:21]([CH3:23])=[O:22])[C@H:7]1[O:24][C:25]([CH3:27])=[O:26])=[O:3].C(N)C1C=CC=CC=1>C1COCC1>[C:17]([O:16][C@@H:9]1[C@@H:8]([O:20][C:21](=[O:22])[CH3:23])[C@@H:7]([O:24][C:25](=[O:26])[CH3:27])[C@@H:6]([CH2:5][O:4][C:2](=[O:3])[CH3:1])[O:11][C@H:10]1[OH:12])(=[O:18])[CH3:19]参加物
4
実験手順
The synthesis of compound 9 is illustrated in FIG. 6. 20 g (51.24 mmol) of β-D-galactosepentaacetate 1 was dissolved in 150 ml THF and 6.7 ml (61.49 mmol) of benzylamine was added with a dropping funnel. The reaction was stirred for 18 h at room temperature to give 2,3,4,6-tetra-O-acetyl-β-D-galactopyranose 2.
出典と根拠
- ORDレコード
- ord-9208ea680a3d4041996f1373e850ba66
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08877917B2
関連ノート
読み込み中…