Enantioselective hydrolysis of cyclopentaneacetic acid esters related to methyl jasmonate

Enantioselective hydrolysis of cyclopentaneacetic acid esters related to methyl jasmonate

The hydrolysis of methyl jasmonate with Aspergillus niger and A. carbonarius is shown to be very dependent upon the particular structure of the substrate. Some variation of the side chain at C-2 is tolerated, whereas the 3-keto group and the methyl ester moieties are particularly important. Porcine...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Enzyme and microbial technology 1993, Vol.15 (10), p.818-820
Hauptverfasser: Kerry, S., Dart, R.K., Marples, B.A.
Format: Artikel
Sprache:eng
Schlagworte:
Aspergillus carbonarius
Aspergillus niger
Bioconversions. Hemisynthesis
Biological and medical sciences
Biotechnology
cyclopentaneacetic acid esters
Enantioselective hydrolysis
Fundamental and applied biological sciences. Psychology
Methods. Procedures. Technologies
methyl jasmonate
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The hydrolysis of methyl jasmonate with Aspergillus niger and A. carbonarius is shown to be very dependent upon the particular structure of the substrate. Some variation of the side chain at C-2 is tolerated, whereas the 3-keto group and the methyl ester moieties are particularly important. Porcine pancreatic lipase, Candida lipase, and Rhizopus lipase are unreactive towards butyl jasmonate.
ISSN:0141-0229
1879-0909
DOI:10.1016/0141-0229(93)90092-G