The DOI matches its Crossref record; 19 of the 19 references it cites were found in a registry or an index.
Generation of Phosphoranyl Radicals via Photoredox Catalysis Enables Voltage–Independent Activation of Strong C–O Bonds
Open accessAbstract
Despite the prevalence of alcohols and carboxylic acids as functional groups in organic molecules and the potential to serve as radical precursors, C-O bonds remain difficult to activate. We report a synthetic strategy for direct access to both alkyl and acyl radicals from these ubiquitous functional groups via photoredox catalysis. This method exploits the unique reactivity of phosphoranyl radicals, generated from a polar/SET crossover between a phosphine radical cation and an oxygen-centered nucleophile. We show the desired reactivity in the reduction of benzylic alcohols to the corresponding benzyl radicals with terminal H atom trapping to afford the deoxygenated products. Using the same method, we demonstrate access to synthetically versatile acyl radicals, which enables the reduction of aromatic and aliphatic carboxylic acids to the corresponding aldehydes with exceptional chemoselectivity. This protocol also transforms carboxylic acids to heterocycles and cyclic ketones via intramolecular acyl radical cyclizations to forge C-O, C-N, and C-C bonds in a single step.
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Citations
Cites
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The Reaction of Trialkyl Phosphites with Thiyl and Alkoxy Radicals1
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Cited by
Kwon, K., Simons, R. T., Nandakumar, M., & Roizen, J. L. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00444 · Cited by 389
Lipshultz, J. M., Li, G., & Radosevich, A. T. (2021) · Journal of the American Chemical Society · doi:10.1021/jacs.0c12816 · Cited by 353
Metadata
- Authors
- Stache, E. E., Ertel, A. B., Rovis, T., & Doyle, A. G.
- Venue
- ACS Catalysis
- Publisher
- American Chemical Society (ACS)
- Published
- 2018-10-18
- Volume
- 8
- Issue
- 12
- Pages
- 11134-11139
- ISSN
- 2155-5435 (ISSN-L)
- OpenAlex
- W2897878623
- Cited by
- 366
- References
- 19
- FWCI
- 10.94
- Type
- journal article
- Language
- en
- Open access
- green
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