http://www.cnr.it/ontology/cnr/individuo/prodotto/ID17716
Chemo-enzymatic synthesis of ethyl ( R )-2-hydroxy-4-phenylbutyrate (Articolo in rivista)
- Type
- Label
- Chemo-enzymatic synthesis of ethyl ( R )-2-hydroxy-4-phenylbutyrate (Articolo in rivista) (literal)
- Anno
- 2010-01-01T00:00:00+01:00 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- DArrigo P., Pedrocchi-Fantoni G., Servi S. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Titolo
- Chemo-enzymatic synthesis of ethyl ( R )-2-hydroxy-4-phenylbutyrate (literal)
- Abstract
- A new biocatalytic strategy to obtain the ethyl (R)-2-hydroxy-4-oxo-4-phenylbutyrate precursor of ethyl
(R)-2-hydroxy-4-phenylbutyrate, an important intermediate in the synthesis of a variety of ACE inhibitors,
has been set up. Starting from ethyl 2,4-dioxo-4-phenylbutyrate, a screen of microorganisms has
been performed in order to find the best catalyst able to reduce the keto group in the a-position with high
chemo- and enantioselectivity. The biotransformation catalyzed by Pichia pastoris CBS 704 gave the best
results in terms of conversion and enantioselectivity. The addition of adsorbing resins in the fermentation
medium is effective in controlling substrate and product concentration in the medium, thus improving
both conversion and enantioselectivity of the biotransformation. Preliminary experiments in a continuous
batch reactor with growing culture of P. pastoris will be also presented (literal)
- Prodotto di
- Autore CNR
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