Unlocking the Accessibility of Alkyl Radicals from Boronic Acids through Solvent-Assisted Organophotoredox Activation
- Prabhat Ranjana
- Serena Pillitteria
- Guglielmo Coppolaa
- Monica Olivaa
- Erik V. Van der Eyckena,b
- Upendra K. Sharmaa
- aLaboratory for Organic & Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven (KU Leuven), Celestijnenlaan 200F, B-3001 Leuven, Belgium
- bPeoples’ Friendship University of Russia (RUDN University), Miklukho-Maklaya Street 6, 117198 Moscow, RussiaRead the publication that featured this abstract
Despite their prevalence in organic synthesis, the application of boronic acids (BAs) as alkyl radical precursors in visible-light-assisted photocatalyzed reactions has been limited by their high oxidation potential. This study demonstrates the prominent ability of amide solvents, namely, N,N-dimethylacetamide, to participate in hydrogen-bonding interactions with BAs, thus enabling the modulation of their oxidation potential toward the generation of alkyl radicals. The developed protocol is simple and robust and demonstrates broad applicability for alkylation, allylation, and elimination reactions in batch and continuous flow. The application toward dehydroalanine allows the synthesis of unnatural amino acids. Furthermore, the chemoselective generation of radical species from BAs in the presence of boronic ester-containing molecules is now feasible, endorsing plausible boron-selective (bio-) orthogonal modifications.
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