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. Author manuscript; available in PMC: 2024 Jun 8.
Published in final edited form as: Chem. 2023 May 4;9(6):1610–1621. doi: 10.1016/j.chempr.2023.04.008

Figure 2. Optimization of carbon–carbon bond formation.

Figure 2.

Reaction conducted using metal salt (3.0 equiv), base (3.0 equiv), nucleophile 2 (3.0 equiv), and carboxylic acid 1 (0.1 mmol) in CH2Cl2 (0.10 M) setup under inert atmosphere and irradiated with a 427 nm blue Kessil Lamp at RT for 24 h. Yields were determined by 1H NMR analysis of the crude reaction mixture using 1-methylnaphthalene as an internal standard. aSee supplemental information for full reaction details. bReaction vessel was wrapped in aluminum foil.