An Efficient Synthesis of the Bicyclic Darunavir Side Chain Using Chemoenzymatic Catalysis

Herein, we describe a chemoenzymatic synthesis of the bicyclic fragment of Darunavir. A ketoreductase was identified using metagenomic mining to catalyze a highly enantio- and diastereoselective dynamic kinetic resolution of a β-ketolactone. Subsequent lactone reduction with diisobutylaluminum hydri...

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Veröffentlicht in:Organic process research & development 2022-07, Vol.26 (7), p.2096-2101
Hauptverfasser: Riehl, Paul S., Lim, Jesmine, Finnigan, James D., Charnock, Simon J., Hyster, Todd K.
Format: Artikel
Sprache:eng
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Zusammenfassung:Herein, we describe a chemoenzymatic synthesis of the bicyclic fragment of Darunavir. A ketoreductase was identified using metagenomic mining to catalyze a highly enantio- and diastereoselective dynamic kinetic resolution of a β-ketolactone. Subsequent lactone reduction with diisobutylaluminum hydride and phase transfer cyclization affords the bicyclic acetal fragment in 39% yield over four steps.
ISSN:1083-6160
1520-586X
DOI:10.1021/acs.oprd.2c00017