The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.
Metal-free C–H alkylation of heteroarenes with alkyltrifluoroborates: a general protocol for 1°, 2° and 3° alkylation
Open accessAbstract
A photoredox-catalyzed C–H functionalization of heteroarenes using a variety of primary, secondary, and tertiary alkyltrifluoroborates is reported.
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Citations
Cites
Fluorine in medicinal chemistry
Purser, S., Moore, P. R., Swallow, S., & Gouverneur, V. (2008) · Chem. Soc. Rev. · doi:10.1039/b610213c · Cited by 7,570
Applications of Fluorine in Medicinal Chemistry
Gillis, E. P., Eastman, K. J., Hill, M. D., Donnelly, D. J., & Meanwell, N. A. (2015) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.5b00258 · Cited by 3,618
Privileged scaffolds for library design and drug discovery
Welsch, M. E., Snyder, S. A., & Stockwell, B. R. (2010) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2010.02.018 · Cited by 1,509
Trifluoromethylation of arenes and heteroarenes by means of photoredox catalysis
Nagib, D. A., & MacMillan, D. W. C. (2011) · Nature · doi:10.1038/nature10647 · Cited by 1,327
Single-electron transmetalation in organoboron cross-coupling by photoredox/nickel dual catalysis
Tellis, J. C., Primer, D. N., & Molander, G. A. (2014) · Science · doi:10.1126/science.1253647 · Cited by 1,281
Self-citationAromatic Nucleophilic Substitution Reactions.
Bunnett, J. F., & Zahler, R. E. (1951) · Chemical Reviews · doi:10.1021/cr60153a002 · Cited by 1,032
Practical and innate carbon–hydrogen functionalization of heterocycles
Fujiwara, Y., Dixon, J. A., O’Hara, F., Funder, E. D., Dixon, D. D., Rodriguez, R. A., Baxter, R. D., Herlé, B., Sach, N., Collins, M. R., et al. (2012) · Nature · doi:10.1038/nature11680 · Cited by 924
Luo, J., & Zhang, J. (2016) · ACS Catalysis · doi:10.1021/acscatal.5b02204 · Cited by 863
Recent Applications of Organic Dyes as Photoredox Catalysts in Organic Synthesis
Nicewicz, D. A., & Nguyen, T. M. (2014) · ACS Catalysis · doi:10.1021/cs400956a · Cited by 856
Innate C-H trifluoromethylation of heterocycles
Ji, Y., Brueckl, T., Baxter, R. D., Fujiwara, Y., Seiple, I. B., Su, S., Blackmond, D. G., & Baran, P. S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1109059108 · Cited by 757
Cited by
Speckmeier, E., Fischer, T. G., & Zeitler, K. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b08933 · Cited by 771
Photocatalytic Late-Stage C–H Functionalization
Bellotti, P., Huang, H.-M., Faber, T., & Glorius, F. (2023) · Chemical Reviews · doi:10.1021/acs.chemrev.2c00478 · Cited by 623
Catalytic enantioselective Minisci-type addition to heteroarenes
Proctor, R. S. J., Davis, H. J., & Phipps, R. J. (2018) · Science · doi:10.1126/science.aar6376 · Cited by 527
Photoelectrochemical C−H Alkylation of Heteroarenes with Organotrifluoroborates
Yan, H., Hou, Z., & Xu, H. (2019) · Angewandte Chemie International Edition · doi:10.1002/anie.201814488 · Cited by 283
Metadata
- Authors
- Matsui, J. K., Primer, D. N., & Molander, G. A.
- Venue
- Chemical Science
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2017
- Volume
- 8
- Issue
- 5
- Pages
- 3512-3522
- ISSN
- 2041-6520 (ISSN-L)
- 2041-6539
- OpenAlex
- W2593124765
- Cited by
- 284
- References
- 37
- FWCI
- 16.80
- Type
- journal article
- Language
- en
- Open access
- diamond
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- CoChat. (2026). Citation check: Metal-free C–H alkylation of heteroarenes with alkyltrifluoroborates: a general protocol for 1°, 2° and 3° alkylation. https://app.cochat.ai/papers/10.1039/c7sc00283a
- The paper
- Matsui, J. K., Primer, D. N., & Molander, G. A. (2017). Metal-free C–H alkylation of heteroarenes with alkyltrifluoroborates: a general protocol for 1°, 2° and 3° alkylation. Chemical Science. https://doi.org/10.1039/c7sc00283a
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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.
