Reaktionsgleichung
O[C:2]1[C:7]([CH:8]=[CH:9][C:10]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[O:11])=[C:6](O)[C:5](O)=[C:4](O)[C:3]=1O.P(O)(O)([O-])=[O:23].C(O)(=O)CC(CC(O)=O)(C(O)=O)O.[Na+]>O>[CH:4]1[CH:5]=[CH:6][C:7](/[CH:8]=[C:9]2/[C:10]([C:12]3[C:17]([O:23]/2)=[CH:16][CH:15]=[CH:14][CH:13]=3)=[O:11])=[CH:2][CH:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In addition, the reaction was carried out under the same conditions using pentahydroxychalcone (PHC) instead of THC as a substrate, and using 0.116 M sodium citrate phosphate buffer (pH 5.4) as a buffer. Similarly, water was used instead of tyrosinase as a control.
Quellen und Nachweise
- ORD-Eintrag
- ord-a95c404bc81a4d1a8327e13d0597751e
- Quelldatensatz
- uspto-grants-2006_01
- Patentnummer
- US06982325B1
Verknüpfte Notizen
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