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Stereoselective Reduction of Prochiral Cyclic 1,3-Diketones Using Different Biocatalysts

Academic Article
Publication Date:
2019
Citation:
Stereoselective Reduction of Prochiral Cyclic 1,3-Diketones Using Different Biocatalysts / M.L. Contente, F. Dall'Oglio, F. Annunziata, F. Molinari, M. Rabuffetti, D. Romano, L. Tamborini, D. Rother, A. Pinto. - In: CATALYSIS LETTERS. - ISSN 1011-372X. - (2019). [Epub ahead of print]
abstract:
We have developed biocatalytic methods for the stereoselective reduction of cyclic prochiral 1,3-diketones for the production of optically active β-hydroxyketones and/or 1,3-diols. The recombinant ketoreductase KRED1-Pglu (formulated as purified catalyst) and whole cells of wild type Escherichia coli DE3 Star were used as biocatalysts, displaying different and sometimes complementary stereoselectivity, thus allowing the preparation of stereochemically pure β-hydroxyketones (12–66% isolated yields, > 99% e.e.) and 1,3-diols (40–60% isolated yields, > 99% e.e.).
IRIS type:
01 - Articolo su periodico
Keywords:
1,3-Diols; 1-3 diketones; Biocatalytic reduction; Enzymatic; Whole cells; β-hydroxyketones
List of contributors:
M.L. Contente, F. Dall'Oglio, F. Annunziata, F. Molinari, M. Rabuffetti, D. Romano, L. Tamborini, D. Rother, A. Pinto
Authors of the University:
CONTENTE MARTINA LETIZIA ( author )
MOLINARI FRANCESCO ENZO ( author )
PINTO ANDREA ( author )
ROMANO DIEGO ( author )
TAMBORINI LUCIA ( author )
Link to information sheet:
https://air.unimi.it/handle/2434/695089
Full Text:
https://air.unimi.it/retrieve/handle/2434/695089/1362436/manuscript%20catalysis%20letters_revised_clean%20copy.pdf
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Concepts (3)


Settore CHIM/06 - Chimica Organica

Settore CHIM/08 - Chimica Farmaceutica

Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni
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