The DOI matches its Crossref record; 19 of the 19 references it cites were found in a registry or an index.
Catalytic cascade reactions by radical relay
Abstract
Catalytic radical relays are an attractive tool for the rapid construction of complex molecular architectures.
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Citations
Cites
Cascade Reactions in Total Synthesis
Nicolaou, K. C., Edmonds, D. J., & Bulger, P. G. (2006) · Angewandte Chemie International Edition · doi:10.1002/anie.200601872 · Cited by 2,101
Catalysis of Radical Reactions: A Radical Chemistry Perspective
Studer, A., & Curran, D. P. (2016) · Angewandte Chemie International Edition · doi:10.1002/anie.201505090 · Cited by 1,266
Efficient Visible Light Photocatalysis of [2+2] Enone Cycloadditions
Ischay, M. A., Anzovino, M. E., Du, J., & Yoon, T. P. (2008) · Journal of the American Chemical Society · doi:10.1021/ja805387f · Cited by 1,167
Radicals: Reactive Intermediates with Translational Potential
Yan, M., Lo, J. C., Edwards, J. T., & Baran, P. S. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b08856 · Cited by 1,098
Photochemical Approaches to Complex Chemotypes: Applications in Natural Product Synthesis
Kärkäs, M. D., Porco, J. A., & Stephenson, C. R. J. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00760 · Cited by 1,017
The recent achievements of redox-neutral radical C–C cross-coupling enabled by visible-light
Xie, J., Jin, H., & Hashmi, A. S. K. (2017) · Chemical Society Reviews · doi:10.1039/c7cs00339k · Cited by 532
Asymmetric catalytic formation of quaternary carbons by iminium ion trapping of radicals
Murphy, J. J., Bastida, D., Paria, S., Fagnoni, M., & Melchiorre, P. (2016) · Nature · doi:10.1038/nature17438 · Cited by 434
[3+2] Cycloadditions of Aryl Cyclopropyl Ketones by Visible Light Photocatalysis
Lu, Z., Shen, M., & Yoon, T. P. (2011) · Journal of the American Chemical Society · doi:10.1021/ja107849y · Cited by 320
Copper‐Catalyzed Radical Cross‐Coupling of Redox‐Active Oxime Esters, Styrenes, and Boronic Acids
Yu, X., Zhao, Q., Chen, J., Chen, J., & Xiao, W. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201809820 · Cited by 238
Enantioselective Photocatalytic [3 + 2] Cycloadditions of Aryl Cyclopropyl Ketones
Amador, A. G., Sherbrook, E. M., & Yoon, T. P. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b01728 · Cited by 217
Total synthesis of complex terpenoids employing radical cascade processes
Hung, K., Hu, X., & Maimone, T. J. (2018) · Natural Product Reports · doi:10.1039/c7np00065k · Cited by 180
Okada, Y., & Chiba, K. (2018) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00400 · Cited by 177
Jiang, H., Lang, K., Lu, H., Wojtas, Ł., & Zhang, X. P. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b05778 · Cited by 157
He, J., Chen, C., Fu, G. C., & Peters, J. C. (2018) · ACS Catalysis · doi:10.1021/acscatal.8b04094 · Cited by 140
Catalytic, Atom‐Economical Radical Arylation of Epoxides
Gansäuer, A., Behlendorf, M., von Laufenberg, D., Fleckhaus, A., Kube, C., Sadasivam, D. V., & Flowers, R. A. I. (2012) · Angewandte Chemie International Edition · doi:10.1002/anie.201200431 · Cited by 139
Zheng, S., Gutiérrez‐Bonet, Á., & Molander, G. A. (2019) · Chem · doi:10.1016/j.chempr.2018.11.014 · Cited by 127
Providing a New Aniline Bioisostere through the Photochemical Production of 1-Aminonorbornanes
Staveness, D., Sodano, T. M., Li, K., Burnham, E. A., Jackson, K. D., & Stephenson, C. R. J. (2018) · Chem · doi:10.1016/j.chempr.2018.10.017 · Cited by 92
Jiang, H., Lang, K., Lu, H., Wojtas, Ł., & Zhang, X. P. (2016) · Angewandte Chemie International Edition · doi:10.1002/anie.201605238 · Cited by 76
Wang, J., & Zheng, N. X. (2015) · Angewandte Chemie International Edition · doi:10.1002/anie.201504076 · Cited by 70
Cited by
Opportunities and Challenges of Metal–Organic Framework Micro/Nano Reactors for Cascade Reactions
Wu, P., Zhao, Y., Zhang, X., Fan, Y., Zhang, S., Zhang, W., & Huo, F. (2023) · JACS Au · doi:10.1021/jacsau.3c00344 · Cited by 48
Metadata
- Authors
- Huang, H.-M., Garduño-Castro, M. H., Morrill, C., & Procter, D. J.
- Venue
- Chemical Society Reviews
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2019
- Volume
- 48
- Issue
- 17
- Pages
- 4626-4638
- ISSN
- 0306-0012 (ISSN-L)
- 1460-4744
- OpenAlex
- W2959631650
- Cited by
- 308
- References
- 19
- FWCI
- 1.73
- Type
- journal article
- Language
- en
- Open access
- closed
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Data sources
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.