The DOI matches its Crossref record; 12 of the 12 references it cites were found in a registry or an index.
Oxalates as Activating Groups for Alcohols in Visible Light Photoredox Catalysis: Formation of Quaternary Centers by Redox-Neutral Fragment Coupling
Open accessAbstract
Alkyl oxalates are new bench-stable alcohol-activating groups for radical generation under visible light photoredox conditions. Using these precursors, the first net redox-neutral coupling of tertiary and secondary alcohols with electron-deficient alkenes is achieved.
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Cites
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Self-citationSolar Synthesis: Prospects in Visible Light Photocatalysis
Schultz, D. M., & Yoon, T. P. (2014) · Science · doi:10.1126/science.1239176 · Cited by 2,586
Shining Light on Photoredox Catalysis: Theory and Synthetic Applications
Tucker, J. W., & Stephenson, C. R. J. (2012) · The Journal of Organic Chemistry · doi:10.1021/jo202538x · Cited by 1,158
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Enantioselective Radical Processes
Sibi, M. P., Manyem, S., & Zimmerman, J. (2003) · Chemical Reviews · doi:10.1021/cr020044l · Cited by 479
Lackner, G. L., Quasdorf, K. W., & Overman, L. E. (2013) · Journal of the American Chemical Society · doi:10.1021/ja408971t · Cited by 316
Self-citationSchnermann, M. J., & Overman, L. E. (2012) · Angewandte Chemie International Edition · doi:10.1002/anie.201204977 · Cited by 274
Self-citationUse of Lewis Acids in Free Radical Reactions
Renaud, P., & Gerster, M. (1998) · Angewandte Chemie International Edition · doi:10.1002/(sici)1521-3773(19981016)37:19<2562::aid-anie2562>3.0.co;2-d · Cited by 267
When C–H bond functionalization meets visible-light photoredox catalysis
Xie, J., Jin, H., Xu, P., & Zhu, C. (2014) · Tetrahedron Letters · doi:10.1016/j.tetlet.2013.10.090 · Cited by 233
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Cited by
Metallaphotoredox: The Merger of Photoredox and Transition Metal Catalysis
Chan, A. Y., Perry, I. B., Bissonnette, N. B., Buksh, B. F., Edwards, G. A., Frye, L. I., Garry, O. L., Lavagnino, M. N., Li, B. X., Liang, Y., et al. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00383 · Cited by 1,754
Self-citationCarbon–Carbon Bond Forming Reactions via Photogenerated Intermediates
Ravelli, D., Protti, S., & Fagnoni, M. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00662 · Cited by 1,109
Tay, N. E. S., Lehnherr, D., & Rovis, T. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00384 · Cited by 518
Strategic Use of Visible-Light Photoredox Catalysis in Natural Product Synthesis
Pitre, S. P., & Overman, L. E. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00247 · Cited by 486
Self-citationStache, E. E., Ertel, A. B., Rovis, T., & Doyle, A. G. (2018) · ACS Catalysis · doi:10.1021/acscatal.8b03592 · Cited by 366
Metadata
- Authors
- Nawrat, C. C., Jamison, C. R., Slutskyy, Y., MacMillan, D. W. C., & Overman, L. E.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2015-08-31
- Volume
- 137
- Issue
- 35
- Pages
- 11270-11273
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W1453281523
- Cited by
- 403
- References
- 12
- FWCI
- 16.78
- Type
- journal article
- Language
- en
- Open access
- green
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- CoChat. (2026). Citation check: Oxalates as Activating Groups for Alcohols in Visible Light Photoredox Catalysis: Formation of Quaternary Centers by Redox-Neutral Fragment Coupling. https://app.cochat.ai/papers/10.1021/jacs.5b07678
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- Nawrat, C. C., Jamison, C. R., Slutskyy, Y., MacMillan, D. W. C., & Overman, L. E. (2015). Oxalates as Activating Groups for Alcohols in Visible Light Photoredox Catalysis: Formation of Quaternary Centers by Redox-Neutral Fragment Coupling. Journal of the American Chemical Society. https://doi.org/10.1021/jacs.5b07678
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
