The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Site-selective arene C-H amination via photoredox catalysis
Abstract
Lighting the way to aryl C-N bonding: Medicinal chemists like to add N bonds to the C atoms of aromatic rings to make bioactive compounds. By harnessing the energy in visible light, Romero et al. made these links and transformed C-H into C-N bonds. They used a blue-absorbing acridinium ion to activate a ring C for an incoming N partner. A nitroxyl radical co-catalyst (TEMPO) then choreographed the transfer of the H atom to O. The reaction worked for a broad range of substrates, including ammonium as a N source. Science , this issue p. 1326
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Citations
Cites
Prier, C. K., Rankic, D. A., & MacMillan, D. W. C. (2013) · Chemical Reviews · doi:10.1021/cr300503r · Cited by 9,590
Cited by
Tay, N. E. S., Lehnherr, D., & Rovis, T. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00384 · Cited by 518
Self-citationDouglas, J. J., Sevrin, M. J., & Stephenson, C. R. J. (2016) · Organic Process Research & Development · doi:10.1021/acs.oprd.6b00125 · Cited by 361
Metadata
- Authors
- Romero, N. A., Margrey, K. A., Tay, N. E., & Nicewicz, D. A.
- Venue
- Science
- Published
- 2015-09-18
- Volume
- 349
- Issue
- 6254
- Pages
- 1326-1330
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2265362920
- Cited by
- 930
- References
- 1
- FWCI
- 35.96
- Type
- journal article
- Language
- en
- Open access
- closed
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- Romero, N. A., Margrey, K. A., Tay, N. E., & Nicewicz, D. A. (2015). Site-selective arene C-H amination via photoredox catalysis. Science. https://doi.org/10.1126/science.aac9895
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