Reaktionsgleichung
[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(O)(=O)CCCCCCCCCCCCCC.[CH:43]1([N:49]=[C:50]=[N:51][CH:52]2[CH2:57][CH2:56][CH2:55]CC2)CCCCC1>O1CCCC1>[CH3:1][N:49]([C:50]1[CH:55]=[CH:56][CH:57]=[CH:52][N:51]=1)[CH3:43]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Following a procedure similar to that described in Example 12, but using 500 mg of radicicol, 830 mg of pentadecanoic acid, 15 ml of dry tetrahydrofuran, 707 mg of dicyclohexylcarbodiimide and a catalytic amount of dimethylaminopyridine, 782 mg of the title compound were obtained.
Quellen und Nachweise
- ORD-Eintrag
- ord-6638c1d13ecf416d8f33623e10da7a25
- Quelldatensatz
- uspto-grants-1997_01
- Patentnummer
- US05597846
Verknüpfte Notizen
Wird geladen…