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.CC1CCCC(C)(C)C=1/C=C/C(/C)=C\C=C\C(\C)=C\C(O)=O.[CH:48]1([N:54]=[C:55]=[N:56][CH:57]2[CH2:62][CH2:61][CH2:60]CC2)CCCCC1>O1CCCC1>[CH3:1][N:54]([C:55]1[CH:60]=[CH:61][CH:62]=[CH:57][N:56]=1)[CH3:48]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Following a procedure similar to that described in Example 12, but using 277 mg of radicicol, 665 mg of trans-vitamin A acid (trans-retinoic acid), 10 ml of dry tetrahydrofuran, 470 mg of dicyclohexylcarbodiimide and a catalytic amount of dimethylaminopyridine, 388 mg of the title compound were obtained.
Quellen und Nachweise
- ORD-Eintrag
- ord-eb678ea0115448fb9f2ef6770f340d19
- Quelldatensatz
- uspto-grants-1997_07
- Patentnummer
- US05650430
Verknüpfte Notizen
Wird geladen…