反応式
[CH3:1][C@H]1OC(=O)C2C(O)=CC(O)=C(Cl)C=2CC(=O)C=CC=C[C@H]2O[C@H]2C1.C[Si](C)(C)CCOCOCCCCCCCCCCCCCCCC(O)=O.[CH:53]1([N:59]=[C:60]=[N:61][CH:62]2[CH2:67][CH2:66][CH2:65]CC2)CCCCC1>O1CCCC1>[CH3:1][N:59]([C:60]1[CH:65]=[CH:66][CH:67]=[CH:62][N:61]=1)[CH3:53]参加物
5
実験手順
Following a procedure similar to that described in Example 12, but using 121 mg of radicicol, 470 mg of 16-[(2-trimethylsilylethoxy)methoxy]hexadecanoic acid, 7 ml of dry tetrahydrofuran, 240 mg of dicyclohexylcarbodiimide and a catalytic amount of dimethylaminopyridine, 481 mg of the title compound were obtained.
出典と根拠
- ORDレコード
- ord-54986dcb837047f3bcb5034468dedfd1
- 出典データセット
- uspto-grants-1997_01
- 特許番号
- US05597846
関連ノート
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