Reaktionsgleichung
[P:1]([O:5][C:6]1[CH:17]=[CH:16][C:9]([CH2:10][C@@H:11]([C:13]([OH:15])=[O:14])[NH2:12])=[CH:8][CH:7]=1)([OH:4])([OH:3])=[O:2].Cl>O1CCCC1>[P:1]([O:5][C:6]1[CH:7]=[CH:8][C:9]([CH2:10][C@@H:11]([C:13]([OH:15])=[O:14])[NH2:12])=[CH:16][CH:17]=1)([OH:3])([OH:4])=[O:2].[NH3:12]Komponenten
5
Edukt 2
Produkt 2
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The tyrosine phosphate derivative VIII when treated with a mixture of 0.1M hydrochloric acid and tetrahydrofuran (1:1) at room temperature for 3 hours gave less than 5% loss of the phosphate group. Treatment of compound VIII with concentrated ammonia in a sealed tube for 5 hours at 60° C. gave rise to complete removal of both 2-cyanoethyl groups with only a trace of loss of phosphate.
Aufarbeitung
- customgave less than 5% loss of the phosphate group
Quellen und Nachweise
- ORD-Eintrag
- ord-debd17f443ba4611b13f3af1e8b81e49
- Quelldatensatz
- uspto-grants-1999_01
- Patentnummer
- US05864032
Verknüpfte Notizen
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