Light-induced palladium catalysis enhances allylic C−H alkylation in internal alkenes, suggesting broader application in natural products.
Tertiary and quaternary carbon centers containing allylic systems are prevalent in natural products and drugs. Among existing approaches toward these valuable motifs, a direct allylic C−H alkylation is the most straightforward approach, which bypasses the requirement for prefunctionalization of allylic substrates. However, existing methods suffer from limited scope both in terms of alkenes and carbon nu-cleophiles. Herein, we report a light-induced Pd photocatalyzed method that overcomes these challenges, enabling the coupling of diverse internal alkenes with a range of carbon pronucleophiles including those with pKa >20. This method provides direct access to the con-struction of tertiary and quaternary carbon centers.
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Pradhan et al. (2025) studied this question.
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