4.8 Article

Redefining the Synthetic Logic of Medicinal Chemistry. Photoredox-Catalyzed Reactions as a General Tool for Aliphatic Core Functionalization

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ORGANIC LETTERS
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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.3c00994

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We present a general approach to synthesis of diversified libraries featuring aliphatic core rings via photoredox catalysis under mild conditions.
C(sp3)-rich aliphatic motifs in drug molecules are strongly associated with clinical success. Historically, the availability of compound libraries based on C(sp3)-rich cores has been limited due to the challenging direct functionalization of aliphatic rings. Instead, most small molecule drug-like libraries are diversified around central aromatic rings. Herein, we present a general approach to the synthesis of diversified libraries featuring aliphatic core rings via photoredox catalysis under mild conditions.

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