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Rapid Communication

Efficient biotransformations in Cunninghamella elegans and Streptomyces sp. JCM9888 of selectively fluorinated benzoic acids to the corresponding benzamides and benzyl alcohols

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Pages 480-484 | Received 21 Aug 2023, Accepted 01 Oct 2023, Published online: 12 Oct 2023

Figures & data

Figure 1. Benzoic 1a–e and 2a–c, phenylacetic 3a–b and cinnamic acids 4a–b used as substrates for biotransformations.

Figure 1. Benzoic 1a–e and 2a–c, phenylacetic 3a–b and cinnamic acids 4a–b used as substrates for biotransformations.

Figure 2. Bioconversions of benzoic acids 12 to benzyl alcohols 56 with Cunninghamella elegans. Conversions (%) are indicated in each case for three day incubations as averages of at least duplicate experiments.

Figure 2. Bioconversions of benzoic acids 1–2 to benzyl alcohols 5–6 with Cunninghamella elegans. Conversions (%) are indicated in each case for three day incubations as averages of at least duplicate experiments.

Figure 3. Biotransformations of aromatic carboxylic acids 1ae, 2ac, 3ab, 4ab to amides 7ae, 8ac, 9ab, 10ab with Streptomyces sp. JCM9888. Conversions are indicated in each case for six day incubations of the various substrates.

Figure 3. Biotransformations of aromatic carboxylic acids 1a–e, 2a–c, 3a–b, 4a–b to amides 7a–e, 8a–c, 9a–b, 10a–b with Streptomyces sp. JCM9888. Conversions are indicated in each case for six day incubations of the various substrates.
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