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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 395256Erstellt: 23. Oktober 2026

L-Leucine → L-Tyrosine

https://huagongshe.com/de/reaction/395256

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktL-LeucineHCID 6106—
EduktL-MethionineHCID 6137—
EduktL-Leucine ethyl esterHCID 75971—
EduktMethyl 2-hydroxybutanoateHCID 520445—
EduktHCID 131724020HCID 131724020—
EduktHCID 131724021HCID 131724021—
ProduktL-TyrosineHCID 6057—
ProduktL-MethionineHCID 6137—

Reaktionsschritte

The papain-catalyzed synthesis of leucine and MHBA co-oligomers was also explored. Synthesis of leucine oligomers and MHBA-leucine co-oligomers was initiated with leucine ethyl ester and MHBA ethyl ester as the substrates. The overall synthesis and purification approach was similar to the one used in the case of methionine and MHBA-methionine. Reaction rates similar to those obtained with methionine and tyrosine were achieved. Approximate oligomer yield was 58%. The freeze-dried oligomers precipitates were solubilized in DMSO. The solution concentration was brought to approximately 2 μg/μl. The solution was mixed with 1:1 acetonitrile:water mixture containing 0.1% acetic acid. The total fluid volume entering the ESI-MS was maintained at 0.2 mL min.−1 The positive mass spectrum of the leucine oligomers is shown in FIG. 33A.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06605590B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-2f5b427d7bed48daa1186d8c9b6dfb35
Quellennotizuspto-grants-2003_08