Rapid Development of a Scalable Reduction of <i>R</i>-Carvone Utilizing Commercially Available Biocatalysts

This work demonstrates the rapid optimization and scale-up of biocatalytic cascades in early development programs, achieving efficient results without the need for lengthy upfront evolution campaigns which are expensive and often do not meet project delivery timelines, which range from 6 to 12 months. By utilizing readily available enzymes, we were able to streamline the process from initial screening to a 100 g reaction, highlighting the feasibility and benefits of this approach in a significantly reduced time frame. Specifically, the ERED- and KRED-catalyzed reduction of R-carvone is described, which allows access to R,R,R-dihydrocarveol with high enantio- and diastereoselectivity under mild conditions.

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Publication Details

Journal
Organic Process Research & Development
Published
2025-05-29
DOI
https://doi.org/10.1021/acs.oprd.5c00116
Citations
2
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
Field-Weighted Citation Impact
1.61
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article

Rapid Development of a Scalable Reduction of R-Carvone Utilizing Commercially Available Biocatalysts

Shane McKenna, Yichen Tan, David T. George
2 citations
Organic Process Research & Development
Enzyme Catalysis and Immobilization
1.61
article

Rapid Development of a Scalable Reduction of R-Carvone Utilizing Commercially Available Biocatalysts

Shane McKenna, Yichen Tan, David T. George
article en
2 citations

Abstract

This work demonstrates the rapid optimization and scale-up of biocatalytic cascades in early development programs, achieving efficient results without the need for lengthy upfront evolution campaigns which are expensive and often do not meet project delivery timelines, which range from 6 to 12 months. By utilizing readily available enzymes, we were able to streamline the process from initial screening to a 100 g reaction, highlighting the feasibility and benefits of this approach in a significantly reduced time frame. Specifically, the ERED- and KRED-catalyzed reduction of R-carvone is described, which allows access to R,R,R-dihydrocarveol with high enantio- and diastereoselectivity under mild conditions.

Organic Process Research & DevelopmentVol. 29(6)
Bristol-Myers Squibb (Germany) (DE), Bristol-Myers Squibb (United States) (US), Bristol-Myers Squibb (United Kingdom) (GB)
Openalex Percentile: Top 17%
Enzyme Catalysis and Immobilization
1.61
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