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DOI: 10.1055/a-2739-0548
Drug Late-Stage Modification by Photocatalytic Conversion of a Carboxyl Group into a Heterocycle
Authors
One-Pot Bioisosteric Replacement of Alkyl Carboxylic Acids via Organic Photoredox Catalysis.
Org. Lett. 2025;
27: 12194-12199
DOI: 10.1021/acs.orglett.5c04049
Keywords
photoredox cyanation - heterocycle installation - late-stage modification - bioisostere replacement
Significance
Nicewicz and co-workers reported a straightforward photocatalytic method for converting drug molecules bearing a carboxyl group into their imidazole bioisosteres. The method was also applied to the synthesis of Flurbiprofen and Fenoprofen oxadiazolone and oxathiadiazolone analogues.
Comment
Replacement of a carboxyl group with its bioisosteres typically requires multistep procedures. Therefore, simple one-step methods, such as that reported by Nicewicz and co-workers, are highly valuable in medicinal chemistry. Their approach provides easy access to three types of bioisosteres directly from the parent drug molecule, greatly simplifying synthesis.
Publication History
Article published online:
16 December 2025
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